Archive for April, 2011

InfuSystem (INFU) Paperless Solutions Enhance Efficiency

MADISON HEIGHTS, Mich., April 14, 2011 (GLOBE NEWSWIRE) — InfuSystem Holdings, Inc. (NYSE Amex:INFU), the leading provider of infusion pumps and associated products and services, today announced the availability of its secure, compliant, paperless solutions. These new solutions allow facilities to create physician work order forms and view treatment logs and patient information. InfuSystem paperless offerings work with customer’s existing workflow and systems and can be accessed anywhere, anytime, from any internet-enabled device.

Customers can increase efficiency by reducing time spent completing traditional paper forms. The process is simplified by linking information across forms and allowing users to add comments and submit corrections instantly. “Reducing the use of paper forms is an important initiative for our customers. We’ve taken the time to develop a paperless system that’s both easy to use and fulfills payers’ documentation and compliance requirements. We’re confident our offering is the most flexible, secure and compliant paperless solution available,” says Sean McDevitt, Chairman and CEO of InfuSystem.

Paperless solutions from InfuSystem are customizable and available across platforms and devices. The secure system protects the privacy of patient data and adheres to patient data compliance regulations. Gaining access to InfuSystem paperless solutions is simple–registration can be done on the website and customers can be up and running quickly. “We’ve found the system to be very intuitive, and the support team has been extremely responsive to our needs. It’s the same service and innovation we’ve come to expect from InfuSystem,” stated Marie Garcia, RN OCN, Director of Clinical Services at Virginia Cancer Specialists.

About InfuSystem Holdings, Inc.

InfuSystem is the leading provider of infusion pumps and related services. InfuSystem services hospitals, oncology practices and other alternate site healthcare providers. Headquartered in Madison Heights, Michigan, InfuSystem delivers local, field-based customer support, and also operates Centers of Excellence in Michigan, Kansas, California, and Ontario, Canada.

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Clearfield (CLFD) Ensures Fiber Protection With Enclosure Line Optimized for Optical Protection

MINNEAPOLIS, April 14, 2011 (GLOBE NEWSWIRE) — Clearfield, Inc. (Nasdaq:CLFDNews), the specialist in fiber management solutions for Fiber to the Premise (FTTp) deployments, is providing an optimized optical protection system with CraftSmart — a full line of above- and below-grade field enclosures. The CraftSmart Fiber Protection Pedestals (FPP) and CraftSmart Fiber Protection Vaults (FPV) are integrated solutions, optimized to house the FieldSmart Small Count Delivery (SCD) Case at the last mile access point of the network in above-grade or below-grade installations.

The combined solution provides an “any application, any media, anywhere” approach to the unique challenges of delivering the last mile drop. The Fiber Protection Vaults (FPV) will also support integration of Clearfield’s FieldSmart Fiber Scalability Center OSP cabinets and traditional splice point slack and closure storage. The CraftSmart line is RUS-listed and is currently shipping.

Integrated Design

“Retrofitting legacy copper solutions in the field is expensive and time-consuming,” explains Johnny Hill, chief operating officer for Clearfield. “Clients have asked for an OSP environmental enclosure line that could reduce the cost of field deployment by providing complete hardware compatibility. CraftSmart optimizes fiber protection and storage while ensuring industry standards. Utilizing tried-and-true methods of sealing and below-grade protection, along with that Clearfield innovation, we have developed a complete, turn-key solution for the deployment of passive optics from the central office/head-end to the customer premise.”

Product Details

The CraftSmart Fiber Protection Pedestal is the industry’s most cost-effective thermoplastic enclosure system featuring a full complement of standard features, including a self-locking security cover and factory installed bracketry. CraftSmart Pedestals are available in two sizes – 9″ x 22″ and 10″ x 24″ – providing maximum work space and bend radius provisions for all passive cables and connectors.

The CraftSmart Fiber Protection Vaults lead the way with 1730, 2436, and 3048 sizes that set new performance standards for below-grade thermoplastic enclosures. Utilizing a straight vertical design that supports the cover’s load across the entire vault, sidewall deflection is neutralized with a high-rib design for utilization in a variety of environments including greenbelt. A factory installed stud system on the interior wall allows for a variety of accessories from storage racks, horizontal brackets, and a two-position swing-arm for mounting Clearfield’s FieldSmart SCD Case onto for easy access and storage.

Video Presentation Available

To learn more about CraftSmart Fiber Protection, an informational video can be viewed at http://www.clearfieldconnection.com/resource-center/demonstration-videos/.

About Clearfield, Inc.

Clearfield, Inc. sets the standard for fiber performance with FiberDeep, while lowering the cost of broadband deployment with the FieldSmart fiber management platform and the CraftSmart OSP enclosure system. FieldSmart is the only fiber management platform to be designed around a single architecture — the Clearview Cassette and xPAK– for the inside plant, outside plant and access network. Scaling from 1 to 1728 ports, FieldSmart supports a wide range of panel and cabinet configurations, densities, connectors and adapter options, and are offered alongside an assortment of passive optical components. CraftSmart is the industry’s only field enclosure system optimized for fiber deployment. FiberDeep is a new class of fiber patch cords that guarantees performance at .2dB insertion loss — fully half that of the industry standard. Clearfield provides a complete line of fiber and copper assemblies for inside plant, outside plant and access networks. Clearfield is a public company traded on NASDAQ: CLFD.

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CDC Global Services (CHINA) and Zhangzhou Development Zone Plan to Invest in High-Tech Food Processing Park

Apr. 14, 2011 (Business Wire) — CDC Global Services, a business unit of CDC Corporation (NASDAQ: CHINA) and a provider of IT and IT-enabled services and consulting, announced that it signed a memorandum of understanding with the Administrative Committee of China Merchant’s Zhangzhou Economic and Technology Development Zone (“China Merchant Group”) to invest in a High-Tech Food Processing Park in that region, as well as to plan projects involving the development of food processing technology solutions and aged care solutions for the China market.

As part of this partnership, CDC Global Services and China Merchant Group plan to set up a R&D center near Xiamen University Campus to develop new software solutions for the food processing industry, focusing on areas such as food safety. As part of this agreement, CDC Global Services and China Merchant Group also plan to host an international food safety IT application seminar in Zhangzhou in the second quarter of 2011. In addition, both organizations plan to study how to use IT to enhance management level and service quality of the aged care market in China. CDC Global Services also expects to leverage the expertise and solutions of CDC Software that offers its Peoplepoint solutions, which enable care suppliers to achieve business efficiencies while improving the quality of care for their elderly residents.

“We are very excited to partner with China Merchant Group to promote food safety and aged care projects in China,” said CK Wong, CEO of CDC Global Services. “We also are creating a model to follow within this region with the collaborative partnership formed between corporate business, government and a higher learning institute. Zhangzhou has agricultural resources which give the food processing industry a solid foundation. That is one reason why we believe this project is a good investment. We also believe our aged care project with China Merchant Group will eventually be ideal for that region when you consider the favorable combination of fine ecological, cultural science, tourism, sports and leisure, entertainment and eco-living resources there. We believe that all of these attributes will contribute to the development of a modern aged people care and services business in China.”

Hu Zheng, executive director of the Administrative Committee of China Merchant’s Zhangzhou Economic and Technology Development Zone and corporate vice president of the China Merchant Group said, “We welcome CDC Global Services’ investment in Zhangzhou. In the past few years, we have made great progress here, however, most of our development was focused on the construction of ports, highways, machinery manufacturing, and metal products. CDC Global Services’ projects represent a milestone for the transition of our industrial structure here.”

Zhangzhou Development Zone is a national development zone and has already completed the industrial layout of three of its core industries: food, machinery and metals manufacturing. Food manufacturing represents a key target industry for Zhangzhou Development Zone.

About CDC Global Services

CDC Global Services provides IT consulting services, including platform-specific services for Microsoft and SAP, as well as project management, staff augmentation, managed-help desk solutions and a full range of business process outsourcing offerings. It can also provide hardware for data collection and RFID, through partnerships with some of the industry’s most reputable vendors. CDC Global Services embraces a customer-first approach being able to draw upon a wide range of expert resources to address each customer’s unique business needs, while keeping their best interest as a top priority. CDC Global Services customers benefit from streamlined vendor management and the ability to control project costs, while being able to access the right IT resources through a singular point of contact. For more information, please visit www.cdcglobalservices.com.

About CDC Corporation

CDC Corporation is a China-based value-added operator of, and growth investor in, hybrid (on premise and SaaS) enterprise software, IT, and new media businesses. The company pursues two value-added investment strategies. The first strategy includes actively managing majority interests in its core portfolio of hybrid enterprise software, IT services and New Media businesses, adding value by driving operational excellence, top-line growth and overall profitability. The second strategy includes identifying and executing on opportunities to co-invest with leading venture capital and private equity funds through minority interests in fast growth companies in emerging markets related to CDC Corporation’s core assets. This second strategy, which complements the first, helps to mitigate risk and enhance deal flow for the company. CDC Corporation expects to deliver superior returns and additional value for its shareholders through these strategies, as well as through its plans to declare and pay regular dividends in the form of registered shares of its publicly listed subsidiaries and other assets. For more information about CDC Corporation (NASDAQ: CHINA), please visit www.cdccorporation.net.

Cautionary Note Regarding Forward-Looking Statements

This press release includes “forward-looking statements” within the meaning of the United States Private Securities Litigation Reform Act of 1995. These forward-looking statements include statements regarding CDC Global Services’ and Zhangzhou Development Zone’s plans, including those to build a high-tech food processing park and establish an R&D center, our expectations regarding expansion with the Zhangzhou Development Zone, our expectations regarding any future plans or projects with the Zhangzhou Development Zone, our expectations regarding involvement of CDC Software in this initiative, our beliefs regarding the benefits of this investment to the Zhangzhou region and the company, including the potential success of this project, our expectations regarding the partnership and high tech park, including the closing thereof and the receipt of any requisite approvals and the satisfaction of any required conditions, and other statements we may make. These statements are based on management’s current expectations and are subject to risks and uncertainties and changes in circumstances. There are important factors that could cause actual results to differ materially from those anticipated in the forward looking statements. If any such risks or uncertainties materialize or if any of the assumptions proves incorrect, our results could differ materially from the results expressed or implied by the forward-looking statements we make. Further information on risks or other factors that could cause results to differ is detailed in filings or submissions with the United States Securities and Exchange Commission made by CDC Corporation in its Annual Report for the year ended December 31, 2009 on Form 20-F filed on June 30, 2010. All forward-looking statements included in this press release are based upon information available to management as of the date of the press release, and you are cautioned not to place undue reliance on any forward looking statements which speak only as of the date of this press release. The company assumes no obligation to update or alter the forward looking statements whether as a result of new information, future events or otherwise. Historical results are not indicative of future performance. For these and other reasons, investors are cautioned not to place undue reliance upon any forward-looking statement in this press release.

CDC Corporation

Investor Relations

Monish Bahl, 678-259-8510

mbahl@cdcsoftware.com

or

Media Relations

Lorretta Gasper, 678-259-8631

lgasper@cdcsoftware.com

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Independent Report Concludes CAMAC Energy, Inc.’s (CAK) OML 120 & 121 Blocks Host Substantial Quantities of Oil

CAMAC Energy Inc., a U.S.-based energy company focused on exploring for, developing and producing oil and gas, was excited to announce today the results of an independent engineering report prepared by Netherland, Sewell & Associates, Inc. (NSAI) for the purpose of estimating the total resource in place at the OML 120 & 121 Blocks situated offshore Nigeria.

The report concluded that the best estimate for gross undiscovered original oil-in-place for OML 120 & 121 is 1.9 billion barrels with a high of 6.3 billion barrels; and the best estimate for associated recoverable gross contingent and unrisked prospective oil resources is 626 million barrels with a high of 2.2 billion barrels. This is substantially greater than the estimated 500 million barrels of potential recoverable oil stated in the company’s recent investor presentation.

“We are pleased to receive this report on resources for the OML 120 & 121 Blocks,” commented Dr. Kase Lawal, Chairman and Chief Executive of CAMAC Energy. “This report clearly supports the potential we see in the two blocks and we are excited about the results. OML 120 & 121 are in a known hydrocarbon province, have existing production, extensive 3D seismic coverage and over a dozen identified prospects and leads. Together with ENI, the technical operator of OML 120 & 121, we will now work towards testing the greater potential of this play, including the deeper Miocene zone.”

The NSAI report, with further information and qualifications, can be found on CAMAC Energy’s website at www.camacenergy.com in the Investor Relations section.

Wednesday, April 13th, 2011 Uncategorized Comments Off on Independent Report Concludes CAMAC Energy, Inc.’s (CAK) OML 120 & 121 Blocks Host Substantial Quantities of Oil

BioTime (BTX) Presents Data at FABS 2011 on the Restoration of Cell Lifespan Using iPS Cell Technology

Apr. 12, 2011 (Business Wire) — BioTime, Inc. (NYSE Amex:BTX) and its subsidiary ReCyte Therapeutics, Inc. announced that today, BioTime CEO Dr. Michael West will present at the French-American Biotech Symposium (FABS 2011) on “New Therapeutic Approaches of Aging” held in San Francisco, CA, showing data for the first time on the restoration of cell lifespan using transcriptional reprogramming technology. Dr. West will speak on “Resetting Telomere Length using Transcriptional Reprogramming and its Application in Age-Related Degenerative Disease” during Session II (2:00-6:30 pm PDT): Innovative Approaches to Age-Related Diseases.On March 16, 2010, BioTime announced the publication of a peer-reviewed scientific article reporting that iPS cell reprogramming technologies could, under certain conditions, reverse the developmental aging of human cells. In other words, through genetic modification, cells from the human body can be reverted back to an embryonic state similar to that of embryonic stem cells, which are capable of developing into all other cell and tissue types. In the same publication, BioTime reported that these reprogramming technologies could reset the telomere clock of cellular aging. Today, Dr. West will be presenting new data validating this technology as it relates to actual cell lifespan. In particular, new evidence will be presented that the technique is capable not only of resetting telomere length, but also of restoring the proliferative lifespan of aged human cells back to that seen in cells obtained from young tissues. Specifically, BioTime scientists measured the replicative lifespan of five human cell types derived from aged human cells that had been returned to the embryonic state using transcriptional reprogramming. These lifespans, which greatly exceeded the normal life expectancy of the original aged cells, provide the first definitive evidence that such technologies provide a means of manufacturing young cells genetically identical to the cells of an aged patient.

“Ever since Dr. Leonard Hayflick’s original observations that human body cells have a finite capacity for cell division, researchers around the world have sought to discover a means to reset that clock for diverse clinical applications,” said Michael D. West, Ph.D., President and Chief Executive Officer of BioTime, Inc. “The rising worldwide demand for novel therapeutics targeting the chronic degenerative diseases of aging makes these new technologies timely, and strategic for the biotechnology industry. We plan to aggressively pursue the commercialization of therapeutic products from this platform, beginning with the vascular products of our ReCyte Therapeutics subsidiary.”

This is the fourth French-American Biotech Symposium co-organized by The Office for Science and Technology of the French Embassy in Washington, DC and Eurobiomed, a French biotech cluster dedicated to health sciences, in partnership with the Gladstone Institute for Virology and Immunology.

Dr. West’s presentation will be available on BioTime’s website at www.biotimeinc.com. For more information on ReCyte Therapeutics, Inc. please visit our website at www.recytecorp.com.

Background:

Regenerative medicine refers to the development and use of therapies based on human embryonic stem (hES) cell or induced pluripotent stem (iPS) cell technology. These therapies will be designed to regenerate healthy tissues to replace tissues afflicted by degenerative diseases. The great scientific and public interest in regenerative medicine lies in the potential of hES and iPS cells to become all of the cell types of the human body. Many scientists therefore believe that hES and iPS cells have considerable potential as sources of new therapies for a host of currently incurable diseases such as diabetes, Parkinson’s disease, heart failure, arthritis, muscular dystrophy, spinal cord injury, macular degeneration, hearing loss, liver failure, and many other disorders where cells and tissues become dysfunctional and need to be replaced.

In 2010, BioTime announced the publication of a peer-reviewed scientific paper titled “Spontaneous Reversal of Developmental Aging in Normal Human Cells Following Transcriptional Reprogramming” in the journal Regenerative Medicine. The discovery that the aging of human cells can be reversed may have significant implications for targeting age-related degenerative disease through the development of new classes of cell-based therapies. The article is available online at www.futuremedicine.com/doi/abs/10.2217/rme.10.21.

BioTime and its collaborators in the article demonstrated the successful reversal of the developmental aging of normal human cells. Normal human cells were induced to reverse the “clock” of differentiation (the process by which an embryonic stem cell becomes the many specialized differentiated cell types of the body), as well as the “clock” of cellular aging (telomere length), using precise genetic modifications. Aged differentiated cells became young stem cells capable of regeneration as a result.

The paper threw some light on the controversy over the aged status of induced pluripotent stem (iPS) cells. The scientific community has been excited over iPS technology as it has been demonstrated to be a means of transforming adult human cells back to a state very similar to that of embryonic stem cells (reversing the process of development) without the use of human embryos. However, there were reports that suggested that iPS cells, though very similar to embryonic stem cells in many respects, may not have the normal replicative potential of embryonic stem cells (i.e., the iPS cells may be prematurely old). This problem has been called “the Achilles heel of iPS cell technology.” In this paper, BioTime scientists and their collaborators showed that many iPS cell lines currently being circulated in the scientific community have short telomeres, meaning that their clock of cellular aging is still set at the age of relatively old cells. However, among these prematurely old cells, other cells can be found with sufficient levels of telomerase (a protein that keeps reproductive cells young) that allow these cells to reverse cellular aging all the way back to the very beginning of the human life cycle.

The research presented in this paper is part of BioTime’s broader research strategy to advance the capabilities of the company’s proprietary ReCyte™ technology, which is being developed as a means of implementing iPS technology on an industrial scale. Whereas the study published in 2010 intentionally used older viral-based means of introducing genes, BioTime now plans further studies of cellular aging reversal using its proprietary ReCyte™ technology specifically designed to rapidly reprogram cells in a manner expected to prevent the telomeric and other genetic abnormalities afflicting previous iPS cell approaches.

About BioTime, Inc.

BioTime, headquartered in Alameda, California, is a biotechnology company focused on regenerative medicine and blood plasma volume expanders. Its broad platform of stem cell technologies is developed through subsidiaries focused on specific fields of applications. BioTime develops and markets research products in the field of stem cells and regenerative medicine, including a wide array of proprietary ACTCellerate™ cell lines, culture media, and differentiation kits. BioTime’s wholly owned subsidiary ES Cell International Pte Ltd (ESI) has produced clinical-grade human embryonic stem cell lines that were derived following principles of Good Manufacturing Practice and currently offers them for use in research. BioTime’s therapeutic product development strategy is pursued through subsidiaries that focus on specific organ systems and related diseases for which there is a high unmet medical need. BioTime’s majority owned subsidiary Cell Cure Neurosciences, Ltd. is developing therapeutic products derived from stem cells for the treatment of retinal and neural degenerative diseases. Cell Cure’s minority shareholder Teva Pharmaceutical Industries has an option to clinically develop and commercialize Cell Cure’s OpRegen™ retinal cell product for use in the treatment of age-related macular degeneration (AMD). BioTime’s subsidiary OrthoCyte Corporation is developing therapeutic applications of stem cells to treat orthopedic diseases and injuries. Another subsidiary, OncoCyte Corporation, focuses on the therapeutic applications of stem cell technology in cancer. ReCyte Therapeutics, Inc. is developing applications of BioTime’s proprietary iPS cell technology to reverse the developmental aging of human cells to treat cardiovascular and blood cell diseases. BioTime’s newest subsidiary, LifeMap Sciences, Inc., is developing an online database of the complex cell lineages arising from hES and iPS cells to guide basic research and to market BioTime’s research products. In addition to its stem cell products, BioTime develops blood plasma volume expanders, blood replacement solutions for hypothermic (low temperature) surgery, and technology for use in surgery, emergency trauma treatment and other applications. BioTime’s lead product, Hextend®, is a blood plasma volume expander manufactured and distributed in the U.S. by Hospira, Inc. and in South Korea by CJ CheilJedang Corp. under exclusive licensing agreements. Additional information about BioTime, ReCyte Therapeutics, Cell Cure, OrthoCyte, OncoCyte, BioTime Asia, and ESI can be found on the web at www.biotimeinc.com.

Forward-Looking Statements

Statements pertaining to future financial and/or operating results, future growth in research, technology, clinical development, and potential opportunities for the company and its subsidiaries, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management constitute forward-looking statements. Any statements that are not historical fact (including, but not limited to statements that contain words such as “will,” “believes,” “plans,” “anticipates,” “expects,” “estimates”) should also be considered to be forward-looking statements. Forward-looking statements involve risks and uncertainties, including, without limitation, risks inherent in the development and/or commercialization of potential products, uncertainty in the results of clinical trials or regulatory approvals, need and ability to obtain future capital, and maintenance of intellectual property rights. Actual results may differ materially from the results anticipated in these forward-looking statements and as such should be evaluated together with the many uncertainties that affect the company’s business, particularly those mentioned in the cautionary statements found in the company’s Securities and Exchange Commission filings. The company disclaims any intent or obligation to update these forward-looking statements.

To receive ongoing BioTime corporate communications, please click on the following link to join our email alert list: http://www.b2i.us/irpass.asp?BzID=1152&to=ea&s=0

BioTime, Inc.

Judith Segall, 510-521-3390 ext. 301

jsegall@biotimemail.com

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TOFUTTI (TOF) Announces 2010 Results

CRANFORD, N.J., April 12, 2011 /PRNewswire/ — TOFUTTI BRANDS INC. (NYSE AMEX Symbol: TOF) issued its results for the fiscal year ended January 1, 2011 today.

Net sales for the fiscal year ended January 1, 2011 were $17,713,000, a decrease of $904,000, or 5%, from the Company’s net sales of $18,617,000, for the fiscal year ended January 2, 2010. The reduction in sales was caused by the continuing difficult general economic conditions and the discontinuance of a number of slower moving, less profitable products during 2010. Although the discontinuance of these slower moving items contributed to reduced sales in fiscal 2010, it also contributed to an improvement in the gross profit percentage for the year. Tofutti’s gross profit percentage increased slightly to 31% in fiscal 2010 from 30% in fiscal 2009.

For fiscal 2010, the Company’s income before income taxes decreased to $802,000 from $835,000 in fiscal 2009, primarily as a result of lower revenues and gross profit, which was partially offset by a reduction in operating expenses. Net income for fiscal 2010 decreased to $462,000 ($0.09 per share) compared to $506,000 ($0.10 per share) for fiscal 2009, primarily as a result of a reduction in operating profit and an increase in income taxes. Income taxes for the 2010 fiscal period were $340,000 compared to $329,000 in fiscal 2009, and the Company’s income tax rate was 42% for the 2010 year compared to 39% in the 2009 fiscal year.

As of January 1, 2011, the Company had cash and cash equivalents of approximately $2.5 million and working capital of approximately $4.4 million compared to cash and cash equivalents of approximately $1.4 million and working capital of approximately $3.9 million at January 2, 2010.

“During the last few fiscal years our industry was subject to significant pricing and economic pressures. We worked hard to maintain the market position of our leading products while shedding slower moving, less profitable products. As a result, we were able to maintain our operating profitability despite a decrease in sales. At the same time, we continued to improve our financial condition as our cash and cash equivalents increased to $2.5 million at January 1, 2011 from $1.4 million at January 2, 2010. Our working capital also improved to $4.4 million at January 1, 2011 from $3.9 million at January 2, 2010.

“Most importantly, we completed the development of two new products that are expected to be rolled out by September of this year. We are very excited about what we believe to be the first commercially available nondairy and gluten-free ricotta cheese product. The second new product is a dairy-free, sugar-free, frozen dessert than incorporates Stevia as the sweetening agent. We believe that the continued market acceptance of our dairy-free, soy based products and the introduction of our new products will drive the growth in our Company’s revenues and profitability in 2011 and the future,” said David Mintz, the Company’s Chairman and CEO.

TOFUTTI BRANDS INC. is principally involved in the development, production and marketing of TOFUTTI brand soy-based, dairy-free frozen desserts, soy-based dairy free cheese products and other soy-based, dairy-free food products. TOFUTTI products are sold in grocery stores, supermarkets, health and convenience stores throughout the United States and in approximately twenty-five other countries.

Some of the statements in this press release concerning the Company’s future prospects are forward-looking statements that involve risks and uncertainties that could cause actual results to differ materially from those in the forward-looking statements. Actual results may vary significantly based upon a number of factors including, but not limited to business conditions both domestic and international, competition, changes in product mix or distribution channels, resource constraints encountered in promoting and developing new products and other risk factors detailed in the Company’s filings with the Securities and Exchange Commission, including its annual report on Form 10-K.

TOFUTTI BRANDS INC.

Statements of Income
(in thousands, except per share figures)

Fiscal Year
ended
January 1, 2011

Fiscal Year
ended
January 2, 2010

Net sales

$17,713

$18,617

Cost of sales

12,271

12,995

Gross profit

5,442

5,622

Operating expenses

4,640

4,787

Income before income taxes

802

835

Income taxes

340

329

Net income

$462

$506

Weighted average number of
shares outstanding:

Basic

5,177

5,177

Diluted

5,177

5,177

Net income per share:

Basic

$0.09

$0.10

Diluted

$0.09

$0.10

TOFUTTI BRANDS INC.

Balance Sheets
(in thousands, except per share figures)

Assets

January 1,
2011

January 2,
2010, restated

Current assets:

Cash and cash equivalents

$2,528

$1,413

Accounts receivable, net of allowance for doubtful

accounts and sales promotions of $320 and $538, respectively

1,338

1,461

Inventories, net

1,697

1,931

Prepaid expenses

16

13

Refundable income taxes

109

Deferred income taxes

186

299

Total current assets

5,765

5,226

Fixed assets (net of accumulated amortization of $33 and $29)

10

15

Other assets

16

16

$5,791

$5,257

Liabilities and Stockholders’ Equity

Current liabilities:

Accounts payable

$ 260

$ 164

Accrued expenses

585

616

Accrued officers’ compensation

500

500

Total current liabilities

1,345

1,280

Commitment and Contingencies

Stockholders’ equity:

Preferred stock – par value $.01 per share;
authorized 100,000 shares, none issued

Common stock – par value $.01 per share;
authorized 15,000,000 shares, issued and
outstanding 5,176,678 shares at January 1, 2011
and 5,176,678 shares at January 2, 2010

52

52

Additional paid-in capital

7

Retained earnings

4,387

3,925

Total stockholders’ equity

4,446

3,977

Total liabilities and stockholders’ equity

$5,791

$5,257

SOURCE TOFUTTI BRANDS INC.

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Intervest Bancshares Corp. (IBCA) Reports 2011 First Quarter Earnings of $1.7 Million

Apr. 12, 2011 (Business Wire) — Intervest Bancshares Corporation (NASDAQ-GS: IBCA), parent company of Intervest National Bank, today reported its financial results for the first quarter of 2011.

Financial Highlights:

  • Net earnings for the first quarter of 2011 (“Q1-11”) amounted to $1.7 million, or $0.08 per diluted common share, compared to a net loss of $2.9 million, or $0.35 per share, for the same quarter a year ago (“Q1-10”) and net earnings of $0.4 million, or $0.02 per share, for the fourth quarter of 2010 (“Q4-10”).
  • Pre-tax earnings before deducting provisions for loan and real estate losses and real estate expenses amounted to $6.3 million in Q1-11, compared to $8.3 million in Q1-10 and $6.6 million in Q4-10.
  • Net interest margin for Q1-11 was 2.14%, compared to 2.23% in Q1-10 and 2.06% in Q4-10.
  • Nonaccrual loans and real estate owned totaled $72 million at March 31, 2011, down 10% from $80 million at December 31, 2010 and 53% from $154 million at March 31, 2010. New non-accrual loans decreased to $5 million in Q1-11, down from $26 million in Q1-10 and $15 million in Q4-10.
  • The total provision for loan and real estate losses decreased to $2.0 million for Q1-11, down substantially from $11.6 million in Q1-10 and $4.7 million in Q4-10. The allowance for loan losses amounted to 2.49% of total outstanding loans at March 31, 2011, compared to 2.61% at December 31, 2010 and 1.73% at March 31, 2010.
  • Noninterest expense amounted to $4.4 million in Q1-11, down from $4.7 million in Q1-10 and $4.9 million in Q4-10. The Company’s efficiency ratio, which is a measure of its ability to control expenses as a percentage of its revenues, was 41% in Q1-11, 42% in Q4-10 and 36% in Q1-10.
  • Intervest National Bank’s regulatory capital ratios continued to improve and were well in excess of the minimums that the Bank has agreed with its regulator to maintain. At March 31, 2011, the Bank’s actual ratios were as follows: total capital to risk-weighted assets – 14.81%; Tier 1 capital to risk-weighted assets – 13.55%; and Tier 1 capital to total average assets (leverage ratio) – 10.04%. The Bank’s minimum required capital ratios are 12%, 10% and 9%, respectively.
  • Common book value per share increased to $7.69 at March 31, 2011 from $7.61 at December 31, 2010.

Net earnings for Q1-11 increased by $4.6 million over Q1-10 due to a $9.6 million decrease in the total provision for loan and real estate losses (reflecting fewer problem assets and credit rating downgrades), a $0.6 million decrease in real estate expenses (reflecting less real estate owned) and a $0.3 million decrease in noninterest expenses (primarily due to lower data processing costs). The aggregate of these items was partially offset by a $2.1 million decrease in net interest and dividend income, a $0.2 million decrease in noninterest income and a $3.6 million increase in tax expense (resulting from pre-tax income in Q1-11 versus a pre-tax loss in Q1-10).

The decrease in net interest and dividend income reflected the planned reduction in the Bank’s assets and liabilities and a slightly lower net interest margin as noted above. Total average interest-earning assets decreased by $305 million in Q1-11 from Q1-10 in part due to the previously reported bulk loan sale in May 2010, with the remainder due to loan payoffs and principal repayments exceeding a reduced volume of new loan originations. These cash inflows were used to fund deposit outflow and repayments of maturing borrowed funds, which positively impacted the Bank’s regulatory capital ratios.

The decrease in the net interest margin in Q1-11 from Q1-10 reflected the impact of the bulk loan sale, a large portion of which included the sale of $108 million of performing troubled debt restructured loans (TDRs) and other loans yielding approximately 5%, payoffs of other higher yielding loans and early calls of U.S. government agency security investments coupled with the reinvestment of the proceeds into similar securities with lower market interest rates, all of which was largely offset by lower rates paid on deposit accounts. The yield on average interest-earning assets decreased by 42 basis points to 4.88% in Q1-11, from 5.30% in Q1-10, while the average cost of funds decreased at nearly the same pace or by 40 basis points to 2.96% in Q1-11, from 3.36% in Q1-10.

Total assets at March 31, 2011 decreased to $2.01 billion from $2.07 billion at December 31, 2010, primarily reflecting a decrease in loans receivable and security investments.

Loans receivable, net of unearned fees, amounted to $1.30 billion at March 31, 2011, a $37 million decrease from $1.34 billion at December 31, 2010. The decrease was due to an aggregate of $39.5 million of principal repayments (resulting from loan payoffs and normal amortization) and $4.5 million of loan chargeoffs, partially offset by $6.6 million of new loan originations. The Company does not own or originate construction/development loans.

Nonaccrual loans and real estate owned aggregated to $72 million, or 3.6% of total assets, at March 31, 2011, compared to $80 million, or 3.9%, at December 31, 2010 and $154 million, or 6.8%, at March 31, 2010. The decrease in total assets since 2009 has negatively impacted the percentages. Nonaccrual loans at March 31, 2011 and December 31, 2010 included $18 million and $21 million, respectively, of performing TDRs that are classified as nonaccrual based on regulatory guidance. These TDRs continue to pay as agreed under their renegotiated terms. As a result of updated appraisals in March 2011, the Bank charged off in Q1-11 a portion of three of these performing TDRs.

The allowance for loan losses at March 31, 2011 was $32.4 million, representing 2.49% of total net loans, compared to $34.8 million, or 2.61%, at December 31, 2010 and $28.3 million, or 1.73%, at March 31, 2010. The overall allowance included specific reserves for impaired loans (comprised of nonaccrual loans and TDRs) at each date of $3.8 million, $7.2 million and $11.0 million, respectively.

Securities held to maturity decreased by $24.4 million to $589.9 million at March 31, 2011 from $614.3 million at December 31, 2010, primarily due to calls exceeding new purchases. The securities portfolio is comprised mainly of U.S. government agency debt securities. At March 31, 2011, the portfolio had a weighted-average yield to earliest call date of 1.64% and a weighted-average remaining contractual maturity of 4.8 years. The Bank invests in U.S. government agency debt obligations to emphasize safety and liquidity. The Company does not own or invest in collateralized debt obligations or collateralized mortgage obligations.

Deposits at March 31, 2011 decreased to $1.71 billion from $1.77 billion at December 31, 2010, reflecting a $46.2 million decrease in time deposits and a $12.8 million decrease in money market deposit accounts.

Borrowed funds and related interest payable at March 31, 2011 decreased to $82 million, from $85 million at December 31, 2010, due to the maturity and repayment of FHLBNY borrowings.

Stockholders’ equity increased to $188 million at March 31, 2011 from $186 million at December 31, 2010, primarily due to the Q1-11 net earnings before preferred dividend requirements of $2.2 million. As required by agreements with its regulators, and as permitted by the underlying documents, the Company has suspended the payment of TARP dividends on its preferred stock and interest on its trust preferred securities since February 2010.

Intervest Bancshares Corporation is a bank holding company. Its principal operating subsidiary is Intervest National Bank, a nationally chartered commercial bank that has its headquarters and full-service banking office at One Rockefeller Plaza, in New York City, and a total of six full-service banking offices in Clearwater and Gulfport, Florida. Intervest Bancshares Corporation’s Class A Common Stock is listed on the NASDAQ Global Select Market: Trading Symbol IBCA. This press release may contain forward-looking information. Words such as “may,” “will,” “could,” “should,” “would,” “believe,” “anticipate,” “estimate,” “expect,” “intend,” “plan,” “project,” “assume,” “indicate,” “continue,” “target,” “goal,” and similar words or expressions of the future are intended to identify forward-looking statements. Except for historical information, the matters discussed herein are subject to certain risks and uncertainties that may affect the Company’s actual results of operations. The following important factors, among others, could cause actual results to differ materially from those set forth in forward looking statements: changes in general economic conditions and real estate values in the Company’s market areas; changes in regulatory policies and enforcement actions; fluctuations in interest rates; demand for loans and deposits; changes in tax laws or the availability of net operating losses, the effects of additional capital, the availability of regulatory waivers; and competition. Reference is made to the Company’s filings with the SEC for further discussion of risks and uncertainties regarding the Company’s business. Historical results are not necessarily indicative of the future prospects of the Company.

Selected Consolidated Financial Information Follows.

INTERVEST BANCSHARES CORPORATION

Selected Consolidated Financial Information

(Dollars in thousands, except per share amounts) Quarter Ended
March 31,
Selected Operating Data: 2011 2010
Interest and dividend income $23,594 $29,631
Interest expense 13,243 17,141
Net interest and dividend income 10,351 12,490
Provision for loan losses 2,045 9,639
Noninterest income 323 512
Noninterest expenses:
Provision for real estate losses 2,001
Real estate expenses 325 976
All other noninterest expenses 4,410 4,689
Earnings (loss) before income taxes 3,894 (4,303 )
Provision (benefit) for income taxes 1,741 (1,825 )
Net earnings (loss) before preferred dividend requirements 2,153 (2,478 )
Preferred dividend requirements (1) 427 409
Net earnings (loss) available to common stockholders $ 1,726 $(2,887 )
Basic earnings (loss) per common share $0.08 $(0.35 )
Diluted earnings (loss) per common share $0.08 $(0.35 )
Average shares used for basic and diluted earnings (loss) per share (2) 21,126,489 8,270,812
Common shares outstanding at end of period 21,126,489 8,270,812
Common stock options/warrants outstanding at end of period 1,045,422 1,018,722
Yield on interest-earning assets 4.88 % 5.30 %
Cost of funds 2.96 % 3.36 %
Net interest margin 2.14 % 2.23 %
Return on average assets (annualized) 0.42 % -0.42 %
Return on average common equity (annualized) 5.29 % -5.20 %
Effective income tax rate 44.71 % 42.41 %
Efficiency ratio (3) 41 % 36 %
Average loans outstanding $1,329,413 $1,680,810
Average securities outstanding 615,357 566,635
Average short-term investments outstanding 17,055 19,145
Average assets outstanding 2,045,999 2,335,592
Average interest-bearing deposits outstanding $1,732,180 $1,961,132
Average borrowings outstanding 81,589 109,028
Average stockholders’ equity 186,823 214,235
At Mar 31, At Dec 31, At Sep 30, At Jun 30, At Mar 31,
Selected Financial Condition Information: 2011 2010 2010 2010 2010
Total assets $ 2,014,125 $ 2,070,868 $ 2,104,098 $ 2,164,442 $ 2,284,257
Cash and short-term investments 29,079 23,911 13,815 35,535 56,470
Securities held to maturity 589,940 614,335 613,844 621,244 491,067
Loans, net of unearned fees 1,300,546 1,337,326 1,363,312 1,395,564 1,634,140
Allowance for loan losses 32,400 34,840 32,250 30,350 28,300
Allowance for loan losses/net loans 2.49 % 2.61 % 2.37 % 2.17 % 1.73 %
Deposits 1,706,630 1,766,083 1,806,834 1,852,356 1,926,772
Borrowed funds and accrued interest payable 82,072 84,676 89,135 98,582 103,060
Preferred stockholder’s equity 23,948 23,852 23,755 23,659 23,563
Common stockholders’ equity 164,243 162,108 140,317 140,643 187,711
Common book value per share (4) 7.69 7.61 15.26 15.33 22.69
Loan chargeoffs for the quarter $ 4,513 $ 386 $ 298 $ 85,483 $ 13,979
Loan recoveries for the quarter 28 283 600
Real estate chargeoffs for the quarter 2,970 912 11,732
Security impairment writedowns for the quarter 105 351 293 18 530
Nonaccrual loans $ 45,192 $ 52,923 $ 38,560 $ 18,927 $ 96,248
Real estate owned, net of valuation allowance 27,064 27,064 38,792 34,259 57,858
Investment securities on a cash basis 4,475 2,318 2,670 2,963 2,981
Accruing troubled debt restructured (TDR) loans (5). 5,630 3,632 617 21,362 116,906
Loans 90 days past due and still accruing 3,879 7,481 16,865 8,788 3,629
Loans 31-89 days past due and still accruing (6) 21,785 11,364 5,264 13,066 14,427
(1) Represents dividend requirements on cumulative preferred stock held by the U.S. Treasury and amortization of related preferred stock discount.
(2) Outstanding options/warrants were not dilutive for the reporting periods.
(3) Represents noninterest expenses (excluding provisions for real estate losses & real estate expenses) as a percentage of net interest and dividend income plus noninterest income.
(4) Represents common stockholders’ equity less preferred dividends in arrears ($1.7 million and $1.4 million at March 31, 2011 and December 31, 2010 only) divided by common shares outstanding.
(5) Represent loans whose terms have been modified mostly through the deferral of principal and/or a partial reduction in interest payments.
(6) At March 31, 2011, these loans were past due 31-59 days. Five loans ($12.3 million) matured – payments are current and extensions are in process, three loans ($6.0 million) are historically slow payers, one loan ($0.9 million) was brought current in April and one loan ($2.6 million) is expected to be extended.
INTERVEST BANCSHARES CORPORATION

Consolidated Financial Highlights

At or For The Period Ended
Quarter Year Year Year Year
($ in thousands, except per share amounts) Ended Ended Ended Ended Ended
Mar 31, Dec 31, Dec 31, Dec 31, Dec 31,
2011 2010 2009 2008 2007
Balance Sheet Highlights:
Total assets $ 2,014,125 $ 2,070,868 $ 2,401,204 $ 2,271,833 $ 2,021,392
Cash and short-term investments 29,079 23,911 7,977 54,903 33,086
Securities held to maturity 589,940 614,335 634,856 475,581 344,105
Loans, net of unearned fees 1,300,546 1,337,326 1,686,164 1,705,711 1,614,032
Allowance for loan losses 32,400 34,840 32,640 28,524 21,593
Allowance for loan losses/net loans 2.49 % 2.61 % 1.94 % 1.67 % 1.34 %
Deposits 1,706,630 1,766,083 2,029,984 1,864,135 1,659,174
Borrowed funds and accrued interest payable 82,072 84,676 118,552 149,566 136,434
Preferred stockholder’s equity 23,948 23,852 23,466 23,080
Common stockholders’ equity 164,243 162,108 190,588 188,894 179,561
Common book value per share (1) 7.69 7.61 23.04 22.84 22.23
Market price per common share 2.55 2.93 3.28 3.99 17.22
Asset Quality Highlights
Nonaccrual loans $ 45,192 $ 52,923 $ 123,877 $ 108,610 $ 90,756
Real estate owned, net of valuation allowance 27,064 27,064 31,866 9,081
Investment securities on a cash basis 4,475 2,318 1,385
Accruing troubled debt restructured loans (2) 5,630 3,632 97,311
Loans past due 90 days and still accruing 3,879 7,481 6,800 1,964 11,853
Loans past due 31-89 days and still accruing 21,785 11,364 5,925 18,943 25,122
Loan chargeoffs 4,513 100,146 8,103 4,227
Loan recoveries 28 883 1,354
Real estate chargeoffs 15,614
Impairment writedowns on security investments 105 1,192 2,258
Statement of Operations Highlights:
Interest and dividend income $ 23,594 $ 107,072 $ 123,598 $ 128,497 $ 131,916
Interest expense 13,243 62,692 81,000 90,335 89,653
Net interest and dividend income 10,351 44,380 42,598 38,162 42,263
Provision for loan losses 2,045 101,463 10,865 11,158 3,760
Noninterest income 323 2,110 297 5,026 8,825
Noninterest expenses:
Provision for real estate losses 15,509 2,275 518
Real estate expenses 325 4,105 4,945 4,281 489
All other noninterest expenses 4,410 19,069 19,864 14,074 12,387
Earnings (loss) before income taxes 3,894 (93,656 ) 4,946 13,157 34,452
Provision (benefit) for income taxes 1,741 (40,348 ) 1,816 5,891 15,012
Net earnings (loss) before preferred dividend requirements 2,153 (53,308 ) 3,130 7,266 19,440
Preferred dividend requirements (3) 427 1,667 1,632 41
Net earnings (loss) available to common stockholders $ 1,726 $ (54,975 ) $ 1,498 $ 7,225 $ 19,440
Basic earnings (loss) per common share $ 0.08 $ (4.95 ) $ 0.18 $ 0.87 $ 2.35
Diluted earnings (loss) per common share $ 0.08 $ (4.95 ) $ 0.18 $ 0.87 $ 2.31
Adjusted net earnings (loss) used to calculatediluted earnings (loss) per common share $ 1,726 $ (54,975 ) $ 1,498 $ 7,225 $ 19,484
Average common shares used to calculate:
Basic earnings (loss) per common share 21,126,489 11,101,196 8,270,812 8,259,091 8,275,539
Diluted earnings (loss) per common share 21,126,489 11,101,196 8,270,812 8,267,781 8,422,017
Common shares outstanding 21,126,489 21,126,489 8,270,812 8,270,812 8,075,812
Net interest margin (4) 2.14 % 2.11 % 1.83 % 1.79 % 2.11 %
Return on average assets 0.42 % -2.42 % 0.13 % 0.34 % 0.96 %
Return on average common equity 5.29 % -32.20 % 1.65 % 3.94 % 11.05 %
Effective income tax rate 44.71 % 43.08 % 36.72 % 44.77 % 43.57 %
Efficiency ratio (5) 41 % 41 % 46 % 33 % 24 %
(1) Represents common stockholders’ equity less preferred dividends in arrears ($1.7 million and $1.4 million at March 31, 2011 and December 31, 2010 only) divided by common shares outstanding.
(2) Represent loans whose terms have been modified mostly through the deferral of principal and/or a partial reduction in interest payments.
(3) Represents dividend requirements on cumulative preferred stock held by the U.S. Treasury and amortization of related preferred stock discount.
(4) Net interest margin is reported exclusive of income from loan prepayments, which is included as a component of noninterest income. Inclusive of such income, the margin would compute to 2.14% for the quarter ended March 31, 2011, 2.32% for 2010, 1.68% for 2009, 1.74% for 2008 and 2.64% for 2007.
(5) Represents noninterest expenses (excluding provisions for real estate losses and real estate expenses) as a percentage of net interest and dividend income plus noninterest income.

Intervest Bancshares Corporation

Lowell S. Dansker, Chairman

Phone 212-218-2800

Fax 212-218-2808

Tuesday, April 12th, 2011 Uncategorized Comments Off on Intervest Bancshares Corp. (IBCA) Reports 2011 First Quarter Earnings of $1.7 Million

Sigma-Aldrich Corp. (SIAL) Division and Kraig Biocraft Laboratories, Inc. (KBLB) to Collaborate for the Production of Spider Silk

Sigma Life Science, the innovative biological products and services research business of Sigma-Aldrich, announced this morning that it has signed an agreement with Kraig Biocraft Laboratories, Inc. to develop genetically modified silkworms for the production of spider silk, using its proprietary CompoZr Zinc Finger Nuclease (ZFN) technology. Transferring silk genes from the spider to the silkworm is anticipated to allow the mass production of stronger silk with enhanced elasticity. Potential applications include sutures, tendon and ligament repair, bulletproof vests, and automobile airbags.

Since the first published sequence of a spider silk gene over twenty years ago, much research has focused on the production of commercially viable spider silk with high tensile strength and elasticity. Last year Kraig Biocraft made an important advance by producing hybrid silkworms with randomly inserted spider silk genes, yielding hybrid spider­silkworm silk with greater strength and durability than native silkworm silk. The precise gene targeting and high efficiency of Sigma’s ZFN technology enables Kraig Biocraft to build on its success by concomitantly targeting the insertion of spider silk genes into the silkworm genome while removing endogenous silkworm silk genes. The resulting transgenic silkworm is believed to be capable of spinning pure spider silk at commercially viable production levels.

“ZFN technology has been revolutionary in genome engineering for various applications, including animal models of disease, engineering of biopharmaceutical production systems, academic research and therapeutics,” stated Dr. Joseph Bedell, Director of Sigma Life Science’s Commercial Animal Technologies Group. “Spider silk production is just the first example of a potential commercial animal application for this exciting technology, perfectly positioning Sigma Life Science as a leading provider of innovative technologies that are changing the face of science and improving the quality of life.”

Tuesday, April 12th, 2011 Uncategorized Comments Off on Sigma-Aldrich Corp. (SIAL) Division and Kraig Biocraft Laboratories, Inc. (KBLB) to Collaborate for the Production of Spider Silk

Cytokinetics (CYTK) Announces Data From Phase IIa “Evidence of Effect” Clinical Trial of CK-2017357

SOUTH SAN FRANCISCO, CA — (Marketwire) — 04/11/11 — Cytokinetics, Incorporated (NASDAQ: CYTK) announced today that an oral presentation of results from its Phase IIa “Evidence of Effect” (EoE) clinical trial of CK-2017357 in patients with amyotrophic lateral sclerosis (ALS) is scheduled to be presented as part of the Clinical Trials Session at the 63rd Annual Meeting of the American Academy of Neurology, to be held April 9-16, 2011 in Honolulu, Hawaii. CK-2017357, a fast skeletal muscle troponin activator, is the lead drug candidate from the company’s skeletal muscle contractility program and the subject of a Phase IIa clinical trials program in patients with ALS, in patients with symptoms of claudication associated with peripheral artery disease, and in patients suffering from myasthenia gravis.

Oral Presentation at the 63rd Annual Meeting of the American Academy of Neurology

Date: Friday, April 15, 2011

Time: 12:15 PM Hawaii-Aleutian Standard Time

Session: 2011 Clinical Trials Session

Location: Hawaii Convention Center in Honolulu, Hawaii

Title: A Phase 2A, Double-Blind, Randomized, Placebo-Controlled, Single-Dose, Crossover Study of the Selective Fast Skeletal Muscle Troponin Activator, CK-2017357, in Patients with ALS

Presenter: Jeffrey M. Shefner, M.D., Ph.D., Professor and Chair, Department of Neurology at the Upstate Medical University, State University of New York

About Cytokinetics

Cytokinetics is a clinical-stage biopharmaceutical company focused on the discovery and development of novel small molecule therapeutics that modulate muscle function for the potential treatment of serious diseases and medical conditions. Cytokinetics’ lead drug candidate from its cardiac muscle contractility program, omecamtiv mecarbil (formerly CK-1827452), is in clinical development for the potential treatment of heart failure. Amgen Inc. holds an exclusive license worldwide (excluding Japan) to develop and commercialize omecamtiv mecarbil and related compounds, subject to Cytokinetics’ specified development and commercialization participation rights. Cytokinetics is independently developing CK-2017357, a skeletal muscle activator, as a potential treatment for diseases and conditions associated with aging, muscle wasting or neuromuscular dysfunction. CK-2017357 is currently the subject of a Phase IIa clinical trials program and has been granted orphan-drug designation by the U.S. Food and Drug Administration for the potential treatment of amyotrophic lateral sclerosis. Cytokinetics is also conducting non-clinical development of compounds that inhibit smooth muscle contractility and which may be useful as potential treatments for diseases and conditions associated with excessive smooth muscle contraction, such as bronchoconstriction associated with asthma and chronic pulmonary obstructive disease. In addition, prior Cytokinetics’ research generated three anti-cancer drug candidates that have progressed into clinical development: ispinesib, SB-743921 and GSK-923295. All of these drug candidates and potential drug candidates have arisen from Cytokinetics’ research activities and are directed towards the cytoskeleton. The cytoskeleton is a complex biological infrastructure that plays a fundamental role within every human cell. Additional information about Cytokinetics can be obtained at www.cytokinetics.com.

This press release contains forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995 (the “Act”). Cytokinetics disclaims any intent or obligation to update these forward-looking statements, and claims the protection of the Act’s safe harbor for forward-looking statements. Examples of such statements include, but are not limited to, statements relating to planned presentations, and the properties and potential benefits of Cytokinetics’ drug candidates and potential drug candidates. Such statements are based on management’s current expectations, but actual results may differ materially due to various risks and uncertainties, including, but not limited to, potential difficulties or delays in the development, testing, regulatory approval and production of Cytokinetics’ drug candidates and potential drug candidates that could slow or prevent clinical development or product approval, including risks that current and past results of clinical trials or preclinical studies may not be indicative of future clinical trials results and that Cytokinetics’ drug candidates and potential drug candidates may have unexpected adverse side effects or inadequate therapeutic efficacy. For further information regarding these and other risks related to Cytokinetics’ business, investors should consult Cytokinetics’ filings with the Securities and Exchange Commission.

Contact:
Christopher S. Keenan
Director, Investor Relations
(650) 624-3000

Monday, April 11th, 2011 Uncategorized Comments Off on Cytokinetics (CYTK) Announces Data From Phase IIa “Evidence of Effect” Clinical Trial of CK-2017357

EFI (EFII) Announces Preliminary First Quarter 2011 Revenue and Earnings Per Share Results

FOSTER CITY, Calif., April 11, 2011 (GLOBE NEWSWIRE) — Electronics For Imaging, Inc. (Nasdaq:EFII), a world leader in customer-focused digital printing innovation, today announced preliminary unaudited results for the quarter ended March 31, 2011. Based on preliminary data, the Company expects to report revenues in the range of $139 million to $140 million and non-GAAP earnings per share (EPS) in the range of $0.27 to $0.28 per share, including a $0.03 benefit from currency. The Company had previously provided an outlook for the first quarter of 2011 of approximately $128 million in revenues, and non-GAAP EPS of $0.14 to $0.16 per share.

Guy Gecht, CEO of EFI, noted that the outstanding preliminary results reflect robust demand across the company’s three business segments, particularly in the Fiery product line. “We were very pleased with the approximately 25% year-over-year increase in revenues, driven by the growth and efficiencies our customers are achieving with EFI’s innovative technology. We continued to see strong customer loyalty for our Fiery digital print servers, along with accelerating demand globally for our software application products. At the same time, the strategic initiatives implemented to improve inkjet margins are showing solid results.”

Commenting on the tragic events in Japan, headquarters for several of EFI’s OEM partners, Gecht continued, “Our hearts go out to the Japanese people. With our long-standing strategic partnerships in Japan, we have developed many close friendships there. We have always had great admiration for the Japanese people’s strength and resilience and are confident in their ability to recover and rebuild. We will continue to monitor the recovery efforts for any potential impact on EFI’s operations or on our OEM partners.”

Q1 2011 Earnings Conference Call Information

EFI will report final, complete financial results on its first quarter 2011 earnings conference call scheduled for April 25, 2011 after the market closes. Investors will be able to access the conference call and slide presentation at the Investor Relations/Events & Presentations portion of EFI’s website at www.efi.com or by phone at (866) 613-9183 for domestic callers and (973) 409-9232 for international callers. The conference call ID is 59047043.

A replay of the webcast will also be available at the aforementioned website following the completion of the call.

About our Non-GAAP Net Income and Adjustments

To supplement our consolidated financial results prepared under generally accepted accounting principles, or GAAP, we use non-GAAP measures of net income (loss) and earnings per diluted share that are GAAP net income (loss) and GAAP earnings per diluted share adjusted to exclude certain recurring and non-recurring costs, expenses and gains.

We believe that the presentation of non-GAAP net income (loss) and non-GAAP earnings per diluted share provides important supplemental information to management and investors regarding non-cash expenses, significant recurring and non-recurring items that we believe are important to understanding our financial and business trends relating to our financial condition and results of operations. Non-GAAP net income (loss) and non-GAAP earnings per diluted share are among the primary indicators used by management as a basis for planning and forecasting future periods and by management and our board of directors to determine whether our operating performance has met specified targets and thresholds. Management uses non-GAAP net income (loss) and non-GAAP earnings per diluted share when evaluating operating performance because it believes that the exclusion of the items described below, for which the amounts and/or timing may vary significantly depending upon the Company’s activities and other factors, facilitates comparability of the Company’s operating performance from period to period. We have chosen to provide this information to investors so they can analyze our operating results in the same way that management does and use this information in their assessment of our business and the valuation of our Company.

We compute non-GAAP net income (loss) and non-GAAP earnings per diluted share by adjusting GAAP net income (loss) and GAAP earnings per diluted share to remove the impact of recurring amortization of acquisition-related intangibles, stock-based compensation expense, as well as restructuring related and non-recurring charges and gains and the tax effect of these adjustments. Such non-recurring charges and gains include end-of-life inventory purchase and related obsolescence, asset impairment charges, acquisition-related transaction costs and legal expenses, and costs to integrate such acquisitions into our business.

These non-GAAP measures are not in accordance with or an alternative for GAAP and may be materially different from other non-GAAP measures, including similarly titled non-GAAP measures, used by other companies. The presentation of this additional information should not be considered in isolation from, as a substitute for, or superior to, net income or earnings per diluted share prepared in accordance with GAAP. Non-GAAP financial measures have limitations in that they do not reflect certain items that may have a material impact upon our reported financial results. We expect to continue to incur expenses of a nature similar to the non-GAAP adjustments described above, and exclusion of these items from our non-GAAP net income (loss) and non-GAAP earnings per diluted share should not be construed as an inference that these costs are unusual, infrequent or non-recurring.

Safe Harbor for Forward Looking Statements

Certain statements in this press release are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended and Section 21E of the Securities Exchange Act of 1934, as amended. Statements other than statements of historical fact including words such as “anticipate”, “believe”, “estimate”, “expect”, “consider” and “plan” and statements in the future tense are forward looking statements. The statements in this press release that could be deemed forward-looking statements include statements regarding EFI’s financial results for the quarter ended March 31, 2011 (including revenues and non-GAAP EPS), EFI’s positioning in the growth segments of digital printing, accelerating demand globally for EFI’s software application products, continuation of the execution of its strategy and momentum, and any statements or assumptions underlying any of the foregoing.

Forward-looking statements are subject to certain risks and uncertainties that could cause our actual future results to differ materially, or cause a material adverse impact on our results. Potential risks and uncertainties include, but are not necessarily limited to, inaccurate data or assumptions; unforeseen expenses; the difficulty of aligning expense levels with revenue changes; execution of actions to reduce our operational costs and ability to maintain effective cost control measures; unexpected declines in revenues or increases in expenses; management’s ability to forecast revenues, expenses and earnings, especially on a quarterly basis; the market prices of the Company’s common stock; the uncertainty regarding the amount and timing of future share repurchases by the Company and the origin of funds used for such repurchases; any world-wide financial and economic difficulties and downturns, including contraction in credit markets and adverse variations in foreign exchange rates, that could affect demand for our products, and increase the volatility of our profitability, as well as the risk of bank failures, insolvency or illiquidity of other financial institutions and other adverse conditions in financial markets that could cause a loss of our cash deposits and invested cash and cash equivalents; uncertainty to accurately predict the outcome of foreign tax audits and determine our tax provisions; uncertainty regarding our effective tax rate in the future that may be impacted by various factors, including but not limited to new U.S. tax legislative proposals; changes in, or the failure or inability to comply with U.S., foreign and local governmental regulations, including import/export regulations or duties; failure to retain key employees; product cancellation costs; a significant decline or delay in demand for our products by any of our important OEM partners; the unpredictability of development schedules and commercialization of the products manufactured and sold by our OEM partners; variations in growth rates or declines in the printing and imaging markets across various geographic regions; changes in historic customer order patterns, including changes in customer and channel inventory levels; changes in the mix of products sold leading to variations in operating results; the uncertainty of market acceptance of new product introductions; delays in product deliveries that cause quarterly revenues and income to fall significantly short of anticipated levels; competition and/or market factors, which may adversely affect margins; competition in each of our businesses, including competition from products internally developed by EFI’s customers; challenge of managing assets levels, including inventory and variations in inventory valuation; intense competition in the industrial and commercial digital inkjet market; the uncertainty of continued success in technological advances, including development and implementation of new processes and strategic products; the challenges of obtaining timely, efficient and quality product manufacturing and components supplying; litigation involving intellectual property rights or other related matters; our ability to successfully integrate acquired businesses, without operational disruption to our existing businesses; the potential that investments in new business strategies and initiatives could disrupt the Company’s ongoing businesses and may present risks not originally contemplated; the potential loss of sales, unexpected costs or adverse impact on relations with customers or suppliers as a result of acquisitions; differences between the financial results as filed with the SEC and the preliminary results included in our earnings or other press releases, among other things, due to the complexity in accounting rules; and any other risk factors that may be included from time to time in the Company’s SEC reports.

The statements in this press release are made as of the date of this press release. EFI undertakes no obligation to update information contained in this press release. For further information regarding risks and uncertainties associated with EFI’s businesses, please refer to the section entitled “Factors That Could Adversely Affect Performance” in the Company’s SEC filings, including, but not limited to, its annual report on Form 10-K and its quarterly reports on Form 10-Q, copies of which may be obtained by contacting EFI’s Investor Relations Department by phone at 650-357-3828 or by email at investor.relations@efi.com or EFI’s Investor Relations website at www.efi.com.

About EFI

EFI (www.EFI.com) is a world leader in customer focused digital printing innovation. EFI’s award-winning solutions, integrated from creation to print, deliver increased performance, cost savings and productivity. The company’s robust product portfolio includes Fiery digital color printer servers; VUTEK superwide digital inkjet printers, UV and solvent inks; Rasktek UV wide-format inkjet printers; Jetrion industrial inkjet printing systems; print production workflow and management information software; and corporate printing solutions.

The Electronics For Imaging, Inc. logo is available at http://www.globenewswire.com/newsroom/prs/?pkgid=7332

CONTACT: Investor Relations Contact:
         JoAnn Horne
         Market Street Partners
         415-445-3235

Electronics For Imaging, Inc. Logo

Monday, April 11th, 2011 Uncategorized Comments Off on EFI (EFII) Announces Preliminary First Quarter 2011 Revenue and Earnings Per Share Results

Level 3 (LVLT) to Acquire Global Crossing (GLBC)

Apr. 11, 2011 (Business Wire) — Level 3 Communications, Inc. (NASDAQ: LVLT) and Global Crossing Limited (NASDAQ: GLBC) today announced that they have entered into a definitive agreement under which Level 3 will acquire Global Crossing in a tax-free, stock-for-stock transaction. The combined company will operate a unique global services platform anchored by fiber optic networks on three continents, connected by extensive undersea facilities. The combined network will serve a worldwide customer set with owned network in more than 50 countries and connections to more than 70 countries. This transaction will create a company with pro forma combined 2010 revenues of $6.26 billion and pro forma combined 2010 Adjusted EBITDA of $1.27 billion before synergies and $1.57 billion after expected synergies.

Under the terms and subject to the conditions of the agreement, Global Crossing shareholders will receive 16 shares of Level 3 common stock for each share of Global Crossing common stock or preferred stock that is owned at closing. Based on Level 3’s closing stock price on April 8, 2011, the transaction is valued at $23.04 per Global Crossing common or preferred share, or approximately $3.0 billion, including the assumption of approximately $1.1 billion of net debt as of Dec. 31, 2010. Global Crossing has approximately 79 million basic and preferred shares outstanding and approximately 83 million shares outstanding on a fully diluted basis, giving effect to outstanding stock awards, but excluding performance-based stock grants.

The transaction will create a company with a unique capability to meet local, national and global customer requirements in a wide range of markets. By combining the strengths of each company, the new entity will offer enterprise, government, wholesale, content, and web-based customers a comprehensive portfolio of end-to-end data, video and voice solutions.

“This is a transformational combination that we believe will deliver significant value to the investors, customers and employees of both Level 3 and Global Crossing,” said Jim Crowe, chief executive officer of Level 3. “The complementary fit between the two companies’ networks, service portfolios and customers is compelling. By leveraging the respective strengths and extensive reach of both companies, we are creating a highly efficient and more extensive global platform that is well-positioned to meet the local and international needs of our customers.”

“This transaction will provide Global Crossing shareholders with an attractive premium and significant participation in the upside potential of a leading communications company with industry-leading scale and capabilities. The combined service capabilities, extensive network assets and talented employees of the two companies will create a stronger global communications competitor with compelling offerings in the marketplace,” said John Legere, chief executive officer of Global Crossing. “Each of our companies has a reputation for being nimble and flexible in meeting customers’ communications needs, and we expect that to continue – with the added benefit of offering customers significantly greater reach, products and services.”

“We’re looking forward to welcoming Singapore Technologies Telemedia, Global Crossing’s largest shareholder, as a significant investor,” said Crowe. “They are exceptionally sophisticated managers, with holdings in telecommunications and information companies in a number of countries. They know the technology and they know the industry. The breadth of their communications experience and their knowledge of international markets will be a great asset to us.”

“This strategic combination is an important milestone for both Global Crossing and Level 3, and a value-creating proposition for all stakeholders,” said Lee Theng Kiat, president and chief executive officer of Singapore Technologies Telemedia (ST Telemedia). “Going forward, we believe the combined strengths of the two companies will position it in a very favorable, competitive position to expand in the U.S. and compete globally.”

“We are committed to creating a high-performing combined business through a carefully managed integration plan executed by a select team from both companies,” said Jeff Storey, president and chief operating officer of Level 3. “We will begin integration planning immediately and bring an aggressive, disciplined approach to the process. After the closing, as we integrate the two operations and work to achieve our expected synergies, we will be dedicated to maintaining our focus on providing excellent customer service and growing our combined revenues.”

“The combination improves our balance sheet and credit profile immediately upon closing with further improvement as we achieve the benefits of integration. Additionally, the transaction accelerates the achievement of Level 3’s target leverage ratio of three to five times debt to Adjusted EBITDA,” said Sunit Patel, chief financial officer of Level 3. “Including the benefit of synergies and the cost of integration, we expect the transaction to be accretive to Level 3’s Free Cash Flow per share in 2013 and to give us the financial strength to capitalize on the many opportunities available in the global market.”

Benefits of the Transaction

Significant Synergy Opportunities

Through integration of the combined businesses, the transaction is expected to create substantial annualized Adjusted EBITDA synergies of approximately $300 million and annualized capital expenditure reduction of approximately $40 million. Level 3 expects to realize approximately two-thirds of the run rate Adjusted EBITDA synergies within 18 months of closing. The company estimates that the net present value of the potential synergies will be approximately $2.5 billion. Of the total expected synergies, approximately 39 percent are from network expense savings, approximately 49 percent from operating expense savings, and approximately 12 percent are from reductions in capital expenditures. The company expects to incur approximately $200 to $225 million of integration costs associated with this transaction. Approximately 55 percent of those costs are expected to be from operating expenses, and 45 percent are expected to be from capital expenditures to support integration activities.

Improved Financial Strength of Combined Business

Including the benefit of synergies and the cost of integration, the transaction is expected to be accretive to Level 3’s Free Cash Flow per share in 2013. As a result of potential revenue growth and synergies, over the longer term, Level 3 expects to have significant Free Cash Flow available for investment in high-return opportunities, including U.S. and international network expansions, and potential repurchase of the company’s securities.

Improvement to Level 3’s Credit Profile

The transaction is expected to improve Level 3’s credit profile as well as significantly strengthen the company’s balance sheet. On a pro forma basis and including the benefit of expected synergies, the ratio of net debt (including capital leases) to Adjusted EBITDA is expected to improve from 6.8x to 4.4x as of Dec. 31, 2010.

Expanded Global Footprint

Existing customers will benefit from expanded geographic reach and a combination of intercity networks and metro networks throughout North America, Latin America and Europe connected by extensive global subsea networks. The combined business will leverage Global Crossing’s long-term IRU’s on the PC1 and EAC cable systems, focusing on telecom operators based in Asia. The combined network will serve a worldwide customer set with owned network in more than 50 countries and reach to more than 70 countries.

Enhanced and Expanded Service Portfolio

The combined business will offer an extensive portfolio of transport, IP and data solutions, content delivery, data center, colocation and voice services, delivered globally. Global Crossing will bring important additions to Level 3’s service portfolio, including managed services, collaboration services and inter-continental virtual private networking capability. The combined service portfolio and distribution channels will allow Level 3 to better address the needs of enterprises, content providers, carriers and governments throughout North America, Latin America and Europe.

Expanded Enterprise Service Capabilities

Global Crossing’s enterprise service portfolio and proven sales expertise together with the improved cost structure and performance achievable by combining the extensive international, intercity and metro networks will enable opportunities for improved growth by giving enterprises better options to meet their local, national and international communications needs.

Committed Financing

Level 3 Financing, Inc., a wholly owned subsidiary of Level 3, has received committed financing for $1.75 billion in connection with this acquisition.

Voting Agreement and Stockholder Rights Agreement

In conjunction with this transaction, Level 3 has signed a Voting Agreement with ST Telemedia, the company which owns approximately 60 percent of Global Crossing’s stock, whereby ST Telemedia has agreed to vote its shares in favor of the transaction, subject to certain terms and conditions. Level 3 and ST Telemedia have also signed a Stockholder Rights Agreement, which becomes effective upon closing and which allows ST Telemedia to designate members to the Level 3 board of directors, proportionate to their stock ownership. In addition, the Stockholder Rights Agreement contains a standstill provision which imposes limitations on ST Telemedia’s ability to purchase or sell Level 3 common stock.

Approvals and Timing of Transaction

In addition to customary closing conditions, the transaction is subject to regulatory approvals relating to competition law, licensing, financing, and foreign ownership, including approvals by the U.S. Department of Justice, the U.S. Federal Communications Commission and other regulatory agencies in the U.S. and in countries where the companies do business. The transaction is also subject to the approval of the stockholders of each company. The transaction is expected to close before the end of this year.

Stockholder Rights Plan

Level 3 also announced separately today that it is adopting a Stockholder Rights Plan (Rights Plan). The Rights Plan is designed to protect Level 3’s federal Net Operating Losses (NOLs) from the effect of Internal Revenue Code Section 382, which can restrict the use of NOLs. The completion of the business combination with Global Crossing would move Level 3 significantly closer to the 50 percent ownership change outlined in Section 382, and increase the likelihood of a loss of Level 3’s valuable NOLs. The rights under the Rights Plan will expire under the circumstances described in the separate release announcing its adoption. In addition, Level 3’s board of directors intends, from time to time (and in particular upon the closing of the transaction), to consider whether maintaining the Rights Plan continues to be in the best interests of Level 3.

Advisors

BofA Merrill Lynch, Citi and Morgan Stanley acted as advisors to Level 3, and Rothschild provided a fairness opinion. Willkie Farr & Gallagher LLP acted as legal counsel to Level 3. Goldman, Sachs & Co. acted as financial advisor and Latham & Watkins acted as legal counsel to Global Crossing. Credit Suisse Securities (USA) LLC acted as financial advisor to ST Telemedia.

Conference Call and Webcast

Level 3 and Global Crossing will hold a joint investor and media conference call to discuss the announcement on April 11 at 9:00 a.m. EDT. To join the call, please dial 888-490-2763 or 719-325-2490, passcode: 9332976. A live webcast of the call can also be heard on Level 3’s website at http://lvlt.client.shareholder.com/events.cfm and at Global Crossing’s website at http://investors.globalcrossing.com. A replay of the call will run for 30 days from April 11, 2011 at 12:00 p.m. CDT until May 11, 2011 at 11:59 p.m. CDT. In order to access that call, please dial 888-203-1112 or 719-457-0820, replay passcode: 9332976.

About Level 3 Communications

Level 3 Communications, Inc. (NASDAQ: LVLT) is a leading international provider of fiber-based communications services. Enterprise, content, wholesale and government customers rely on Level 3 to deliver services with an industry-leading combination of scalability and value over an end-to-end fiber network. Level 3 offers a portfolio of metro and long-haul services, including transport, data, Internet, content delivery and voice. For more information, visit www.level3.com.

© Level 3 Communications, LLC. All Rights Reserved. Vyvx, Venuenet+, Level 3, Level 3 Communications and the Level 3 Communications Logo are either registered service marks or service marks of Level 3 Communications, LLC and/or one of its Affiliates in the United States and/or other countries. Level 3 services are provided by wholly owned subsidiaries of Level 3 Communications, Inc.

About Global Crossing

Global Crossing (NASDAQ: GLBC) is a leading global IP, Ethernet, data center and video solutions provider with the world’s first integrated global IP-based network. The company offers a full range of data, voice, collaboration, broadcast and media services delivered with superior customer service.

Global Crossing provides services to enterprises (including approximately 40 percent of the Fortune 500); government departments and agencies; and 700 carriers, mobile operators and ISPs. It delivers converged IP services to more than 700 cities in more than 70 countries, and has 17 world-class data centers in major business centers around the globe.

Please visit www.globalcrossing.com for more information about Global Crossing.

Forward Looking Statements About Global Crossing

This press release contains statements about expected future events and financial results that are forward looking and subject to risks and uncertainties that could cause the actual results to differ materially, including: the failure to occur of any condition to the closing of the acquisition of Global Crossing by Level 3, including the failure to obtain a required approval or the experiencing of a material adverse effect by either company; the failure to achieve expected synergies from the acquisition; Global Crossing’s history of substantial operating losses and the fact that, in the near term, funds from operations will not satisfy cash requirements; the availability of future borrowings in an amount sufficient to pay Global Crossing’s indebtedness and to fund its other liquidity needs; legal and contractual restrictions on the inter-company transfer of funds by Global Crossing’s subsidiaries; Global Crossing’s ability to continue to connect its network to incumbent carriers’ networks or maintain Internet peering arrangements on favorable terms; the consequences of any inadvertent violation of Global Crossing’s Network Security Agreement with the U.S. Government; increased competition and pricing pressures resulting from technology advances and regulatory changes; competitive disadvantages relative to competitors with superior resources; political, legal and other risks due to Global Crossing’s substantial international operations; risks associated with movements in foreign currency exchange rates; risks related to restrictions on the conversion of the Venezuelan bolivar into U.S. dollars and to the resultant buildup of a material excess bolivar cash balance, which is carried on Global Crossing’s books at the official exchange rate, attributing to the bolivar a value that is significantly greater than the value that would prevail on an open market; potential weaknesses in internal controls of acquired businesses, and difficulties in integrating internal controls of those businesses with Global Crossing’s own internal controls; exposure to contingent liabilities; and other risks referenced from time to time in Global Crossing’s filings with the Securities and Exchange Commission. Global Crossing undertakes no duty to update information contained in this press release or in other public disclosures at any time.

About Singapore Technologies Telemedia

Singapore Technologies Telemedia (ST Telemedia) invests in and manages an innovative group of information-communications companies across the globe. Its core competencies are in mobile communications and global IP services. Key companies in the ST Telemedia group include Global Crossing, a leading global IP and Ethernet solutions provider with the world’s first integrated global IP-based network; eircom, one of Ireland’s largest telecommunications operators; U Mobile Sdn Bhd, Malaysia’s 3G operator; TeleChoice, a leading regional diversified provider and enabler of innovative communication solutions; ST Teleport, Asia’s leading full-service satellite communications solution provider; VNPT Global, the leading company of VNPT in international business and Asia Mobile Holdings which holds interests in StarHub, Singapore’s fully-integrated info-communication company; and Shenington Investments

Important Information For Investors And Stockholders

This communication shall not constitute an offer to sell or the solicitation of an offer to buy any securities or a solicitation of any vote or approval. The proposed transaction will be submitted to the stockholders of Level 3, Inc. (“Level 3”) and the stockholders of Global Crossing Limited (“Global Crossing”) for their consideration. Level 3 and Global Crossing will file a registration statement on Form S-4, a joint proxy statement/prospectus and other relevant documents concerning the proposed transaction with the SEC. Level 3 and Global Crossing will each provide the final joint proxy statement/prospectus to its respective stockholders. Investors and security holders are urged to read the registration statement and the joint proxy statement/prospectus and any other relevant documents filed with the SEC when they become available, as well as any amendments or supplements to those documents, because they will contain important information about Level 3, Global Crossing and the proposed transaction. Investors and security holders will be able to obtain a free copy of the registration statement and joint proxy statement/prospectus, as well as other filings containing information about Level 3 and Global Crossing free of charge at the SEC’s Web Site at http://www.sec.gov. In addition, the joint proxy statement/prospectus, the SEC filings that will be incorporated by reference in the joint proxy statement/prospectus and the other documents filed with the SEC by Level 3 may be obtained free of charge by directing such request to: Investor Relations, Level 3, Inc., 1025 Eldorado Boulevard, Broomfield, Colorado 80021 or from Level 3’s Investor Relations page on its corporate website at http://www.Level3.com and the joint proxy statement/prospectus, the SEC filings that will be incorporated by reference in the joint proxy statement/prospectus and the other documents filed with the SEC by Global Crossing be obtained free of charge by directing such request to: Global Crossing by telephone at (800) 836-0342 or by submitting a request by e-mail to glbc@globalcrossing.com or a written request to the Secretary, Wessex House, 45 Reid Street, Hamilton HM12 Bermuda or from Global Crossing’s Investor Relations page on its corporate website at http://www.globalcrossing.com.

Level 3, Global Crossing and their respective directors, executive officers, and certain other members of management and employees may be deemed to be participants in the solicitation of proxies in favor of the proposed transactions from the stockholders of Level 3 and from the stockholders of Global Crossing, respectively. Information about the directors and executive officers of Level 3 is set forth in the proxy statement on Schedule 14A for Level 3’s 2011 Annual Meeting of Stockholders, which was filed with the SEC on April 4, 2011 and information about the directors and executive officers of Global Crossing is set forth in the proxy statement for Global Crossing’s 2010 Annual Meeting of Stockholders, which was filed with the SEC on May 19, 2010. Additional information regarding participants in the proxy solicitation may be obtained by reading the joint proxy statement/prospectus regarding the proposed transaction when it becomes available.

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, (i) statements about the benefits of the acquisition of Global Crossing by Level 3, including financial and operating results and synergy benefits that may be realized from the acquisition and the timeframe for realizing those benefits; Level 3’s and Global Crossing’s plans, objectives, expectations and intentions and other statements contained in this communication that are not historical facts; and (ii) other statements identified by words such as “expects,” “anticipates,” “intends,” “plans,” “believes,” “seeks,” “estimates” or words of similar meaning.

These forward-looking statements are based upon management’s current beliefs or expectations and are inherently subject to significant business, economic and competitive uncertainties and contingencies and third-party approvals, many of which are beyond our control. The following factors, among others, could cause actual results to differ materially from those expressed or implied in the forward-looking statements: (1) the occurrence of any event, change or other circumstances that could give rise to the termination of the Agreement and Plan of Amalgamation among Level 3, Global Crossing and Global Crossing Amalgamation Sub, Ltd. (the “Amalgamation Agreement”); (2) the inability to complete the transactions contemplated by the Amalgamation Agreement due to the failure to obtain the required stockholder approvals; (3) the inability to satisfy the other conditions specified in the Amalgamation Agreement, including without limitation the receipt of necessary governmental or regulatory approvals required to complete the transactions contemplated by the Amalgamation Agreement; (4) the inability to successfully integrate the businesses of Level 3 and Global Crossing or to integrate the businesses within the anticipated timeframe; (5) the risk that the proposed transactions disrupt current plans and operations, increase operating costs and the potential difficulties in customer loss and employee retention as a result of the announcement and consummation of such transactions; (6) the ability to recognize the anticipated benefits of the combination of Level 3 and Global Crossing, including the realization of revenue and cost synergy benefits; and to recognize such benefits within the anticipated timeframe; (7) the outcome of any legal proceedings that may be instituted against Level 3, Global Crossing or others following announcement of the Amalgamation Agreement and transactions contemplated therein; and (8) the possibility that Level 3 or Global Crossing may be adversely affected by other economic, business, and/or competitive factors.

Other important factors that may affect Level 3’s and the combined business’ results of operations and financial condition include, but are not limited to: the current uncertainty in the global financial markets and the global economy; a discontinuation of the development and expansion of the Internet as a communications medium and marketplace for the distribution and consumption of data and video; disruptions in the financial markets that could affect Level 3’s ability to obtain additional financing, and the company’s ability to: increase and maintain the volume of traffic on its network; develop effective business support systems; manage system and network failures or disruptions; develop new services that meet customer demands and generate acceptable margins; defend intellectual property and proprietary rights; adapt to rapid technological changes that lead to further competition; attract and retain qualified management and other personnel; successfully integrate acquisitions; and meet all of the terms and conditions of debt obligations.

Additional information concerning these and other important factors can be found within Level 3’s and Global Crossing’s respective filings with the SEC, which discuss the foregoing risks as well as other important risk factors that could contribute to such differences or otherwise affect our business, results of operations and financial condition. Statements in this communication should be evaluated in light of these important factors. The forward-looking statements in this communication speak only as of the date they are made. Except for the ongoing obligations of Level 3 and Global Crossing to disclose material information under the federal securities laws, neither Level 3 nor Global Crossing undertakes any obligation to, and expressly disclaim any such obligation to, update or alter any forward-looking statement to reflect new information, circumstances or events that occur after the date such forward-looking statement is made unless required by law.

Non-GAAP Metrics

Pursuant to Regulation G, the company is hereby providing a reconciliation of non-GAAP financial metrics to the most directly comparable GAAP measure.

The following describes and reconciles those financial measures as reported under accounting principles generally accepted in the United States (GAAP) with those financial measures as adjusted by the items detailed below and presented in the accompanying news release. These calculations are not prepared in accordance with GAAP and should not be viewed as alternatives to GAAP. In keeping with its historical financial reporting practices, the company believes that the supplemental presentation of these calculations provides meaningful non-GAAP financial measures to help investors understand and compare business trends among different reporting periods on a consistent basis, independently of regularly reported non-cash charges and infrequent or unusual events.

Combined Total Revenue is defined as combined total revenue from the Consolidated Statements of Operations as filed in each company’s Annual Report on Form 10-K for the year ended December 31, 2010.

Communications Revenue is defined as communications revenue from Level 3 Communications’ Consolidated Statements of Operations.

Adjusted EBITDA is defined as net income (loss) from the Consolidated Statements of Operations before income taxes, total other income (expense), non-cash impairment charges, depreciation and amortization and non-cash stock compensation expense.

Adjusted EBITDA plus Estimated Synergies is defined as Adjusted EBITDA plus the estimated synergies resulting from the combination.

Total Debt, including Capital Leases is defined as the current and long-term portions of debt and obligations under capital leases as reported in the Consolidated Balance Sheets filed in each company’s Annual Report on Form 10-K for the year ended December 31, 2010.

Cash and Cash Equivalents is defined as the total cash and cash equivalents reported as a component of current assets in the Consolidated Balance Sheets as filed in each company’s Annual Report on Form 10-K for the year ended December 31, 2010.

Debt to Adjusted EBITDA Ratio is defined as Total Debt, including Capital Leases divided by Adjusted EBITDA.

Net Debt to Adjusted EBITDA Ratio is defined as Total Debt, including Capital Leases reduced by the Cash and Cash Equivalents, divided by Adjusted EBITDA.

Combined Revenue Year Ended December 31, 2010
($ in millions) Level 3

Communications

Global

Crossing

Combined
Revenue:
Communications $ 3,591 $ 2,609 $ 6,200
Coal 60 60
Total Revenue $ 3,651 $ 2,609 $ 6,260
Adjusted EBITDA Metrics Year Ended December 31, 2010
Level 3

Communications

Global

Crossing

Combined
($ in millions) Communications Other Consolidated Consolidated
Net Loss applicable to common shareholders ($617 ) ($5 ) ($622 ) ($176 ) $ (798 )
Preferred Stock Dividends 4 4
Income Tax Benefit (91 ) (91 ) (5 ) (96 )
Total Other (Income) Expense 620 3 623 240 863
Depreciation and Amortization 870 6 876 337 1,213
Non-cash Stock Compensation 67 67 20 87
Adjusted EBITDA $ 849 $ 4 $ 853 $ 420 $ 1,273
Estimated Synergies $ 300
Adjusted EBITDA plus Estimated Synergies $ 1,573
Adjusted EBITDA Ratios Year Ended December 31, 2010
($ in millions) Level 3 Communications Global Crossing Combined Combined with Synergies
Total Debt, including capital leases $ 6,448 $ 1,461 $ 7,909 $ 7,909
Cash and cash equivalents (616 ) (372 ) (988 ) (988 )
Net Debt $ 5,832 $ 1,089 $ 6,921 $ 6,921
Adjusted EBITDA $ 853 $ 420 $ 1,273 $ 1,573
Debt to Adjusted EBITDA Ratio 7.56 3.48 6.21 5.03
Net Debt to Adjusted EBITDA Ratio 6.84 2.59 5.44 4.40

Management believes that Adjusted EBITDA and Adjusted EBITDA plus Estimated Synergies are relevant and useful metrics to provide to investors, as they are an important part of the company’s internal reporting and are key measures used by Management to evaluate profitability and operating performance of the company and to make resource allocation decisions. Management believes such measures are especially important in a capital-intensive industry such as telecommunications. Management also uses Adjusted EBITDA and Adjusted EBITDA plus Estimated Synergies to compare the company’s performance to that of its competitors and to eliminate certain non-cash and non-operating items in order to consistently measure from period to period its ability to fund capital expenditures, fund growth, service debt and determine bonuses. Adjusted EBITDA excludes non-cash impairment charges and non-cash stock compensation expense because of the non-cash nature of these items. Adjusted EBITDA also excludes interest income, interest expense and income taxes because these items are associated with the company’s capitalization and tax structures. Adjusted EBITDA also excludes depreciation and amortization expense because these non-cash expenses reflect the impact of capital investments which management believes should be evaluated through free cash flow. Adjusted EBITDA excludes the gain (or loss) on extinguishment of debt and other, net because these items are not related to the primary operations of the company.

There are limitations to using non-GAAP financial measures, including the difficulty associated with comparing companies that use similar performance measures whose calculations may differ from the company’s calculations. Additionally, this financial measure does not include certain significant items such as interest income, interest expense, income taxes, depreciation and amortization, non-cash impairment charges, non-cash stock compensation expense, the gain (or loss) on extinguishment of debt and net other income (expense). Adjusted EBITDA and Adjusted EBITDA plus Estimated Synergies should not be considered a substitute for other measures of financial performance reported in accordance with GAAP.

Free Cash Flow is defined as net cash provided by (used in) operating activities less capital expenditures as disclosed in the Consolidated Statements of Cash Flows in each company’s Annual Report on Form 10-K for the year ended December 31, 2010. Management believes that Free Cash Flow and Free Cash Flow plus Estimated Synergies are relevant metrics to provide to investors, as it is an indicator of the company’s ability to generate cash to service its debt. Free Cash Flow excludes cash used for acquisitions and principal repayments.

There are material limitations to using Free Cash Flow to measure the company against some of its competitors as Level 3 does not currently pay a significant amount of income taxes due to net operating losses, and therefore, generates higher cash flow than a comparable business that does pay income taxes. Additionally, this financial measure is subject to variability quarter over quarter as a result of the timing of payments related to accounts receivable and accounts payable and capital expenditures. This financial measure should not be used as a substitute for net change in cash and cash equivalents on the Consolidated Statements of Cash Flows.

Free Cash Flow Year Ended December 31, 2010
($ in millions) Level 3

Communications

Global

Crossing

Combined Combined

with Synergies

Net Cash Provided by Operating Activities $ 339 $ 183 $ 522 $ 822
Capital Expenditures (436 ) (167 ) (603 ) (563 )
Free Cash Flow $ (97 ) $ 16 $ (81 ) $ 259

Level 3 Media Contact:

Josh Howell, + 1 720-888-3912

Media.Relations@level3.com

or

Level 3 Investor Contact:

Mark Stoutenberg, + 1 720-888-1662

Investor.Relations@level3.com

or

Global Crossing Media Contact:

Michael Schneider, + 1 973-937-0146

Michael.Schneider@globalcrossing.com

or

Global Crossing Investor Contact:

Mark Gottlieb, + 1 800-836-0342

glbc@globalcrossing.com

Monday, April 11th, 2011 Uncategorized Comments Off on Level 3 (LVLT) to Acquire Global Crossing (GLBC)

Flowers Foods (FLO) and Tasty Baking Company (TSTY) Announce All Cash Merger Agreement

THOMASVILLE, Ga. and PHILADELPHIA, April 11, 2011 /PRNewswire/ — Flowers Foods (NYSE: FLO) (“Flowers”) and Tasty Baking Company (NasdaqGM: TSTY) (“Tasty”) today announced a definitive merger agreement whereby Flowers will acquire all of the outstanding shares of Tasty common stock for $4.00 per share in cash for a total purchase price of approximately $165 million, including Tasty’s existing indebtedness.

(Logo: http://photos.prnewswire.com/prnh/20080530/CLF007LOGO )

The transaction is expected to:

  • Strengthen Flowers’ snack cake business through the addition of the iconic Tastykake snack cake brand;
  • Expand Flowers’ geographic reach, immediately adding more than 24 million consumers who are contiguous with Flowers’ current footprint;
  • Add two highly efficient bakeries with additional capacity to support growth;
  • Generate significant operating synergies through additional revenue and cost-saving opportunities;
  • Add approximately $115 million to $125 million to Flowers’ 2011 sales, contribute approximately $10 million to $12 million to Flowers’ 2011 EBITDA, and be neutral to slightly accretive to 2011 earnings per share, excluding one-time costs of the transaction; and
  • Contribute approximately $210 million to $225 million to Flowers’ 2012 sales, contribute approximately $25 million to $30 million to 2012 EBITDA, and contribute approximately $.06 to $.09 per diluted share.

Under the terms of the agreement, Flowers will commence a tender offer to acquire all of the outstanding shares of Tasty common stock for $4.00 per share in cash. The transaction is expected to close during the second quarter of 2011 and is subject to customary closing conditions and approvals, as well as a majority of the outstanding shares of Tasty common stock being validly tendered and not withdrawn in the tender offer. The agreement has been unanimously approved by the Boards of Directors of both companies. Flowers intends to fund the transaction through cash-on-hand and credit facilities. There is no financing condition to the offer. Upon completion of the transaction, Tasty will become part of Flowers’ direct-store-delivery segment.

“We are very pleased with the addition of Tasty to Flowers,” said George E. Deese, Flowers Foods’ Chairman and CEO. “Tasty brings a talented, committed team of employees, two highly efficient bakeries, the iconic Tastykake brand, a solid sales base, and an effective distribution system. The merger will expand Flowers’ geographic reach and bring new consumers, new customers, and new opportunities for further growth. It will provide the opportunity to add Tastykake products to Flowers’ existing direct-store-delivery network. With the addition of Tasty, our snack cake business will be significantly enhanced and we will have a new platform to grow our Nature’s Own brand as we make other acquisitions that add needed production capacity for breads, buns, and rolls.

“Tasty and Flowers have a similar heritage and share the same core values of integrity, service, quality, and commitment,” Deese continued. “We are delighted to welcome Tasty’s 740 dedicated employees and 413 independent sales distributors to the Flowers Foods family. Our plans are to invest in the combined business for sustainable and profitable growth, and they will be an important part of Flowers’ ongoing success.”

Charles P. Pizzi, Tasty’s President and CEO, said, “This merger with Flowers will create value for Tasty’s shareholders, employees, and the Philadelphia community. It will provide immediate cash value to our stockholders at an attractive premium over the current trading value. We believe the combination of Tasty with Flowers will create a company with long-term advantages for our employees, customers, suppliers, independent sales distributors, and other constituents. Flowers also shares Tasty’s commitment to the communities in which it operates. We have a deep respect for Flowers’ approach to managing its business and employees, and we look forward to working closely with the Flowers team to complete the merger as quickly as possible and to ensure a smooth transition.”

Expected Benefits of the Flowers and Tasty Combination

The combination of Flowers and Tasty leverages their complementary product offerings and market strengths and unites two companies with rich traditions of delivering quality and value to their customers and consumers. This combination is expected to result in:

  • Creation of a larger business with a complementary portfolio of high-quality branded and store-brand bakery products;
  • A deeper penetration of the snack cake category, which should strengthen customer relationships over a broader geography;
  • The ability to grow the Tastykake brand in its current markets and provide new opportunities for Tastykake’s independent sales distributors;
  • The opportunity to expand distribution of the Tastykake brand through the majority of Flowers’ 4,000 independent distributors, whose existing territories have access to 53 percent of the U.S. population;
  • The addition of two highly efficient bakeries strategically located in the heart of the Northeast corridor. The available snack cake capacity in these state-of-the-art facilities provides a platform for further profitable growth;
  • The immediate addition of approximately 24 million consumers who are contiguous to Flowers Foods’ existing geographic footprint, which will increase Flowers’ market access to about 61 percent of the U.S. population through its direct-store-delivery systems;
  • The potential to expand the reach of Flowers’ Nature’s Own brand through Tasty’s marketing areas as Flowers continues to expand and acquire additional production capacity for bread, buns and rolls; and
  • A strong, combined financial profile, with an anticipated sales contribution from the transaction of $115 million to $125 million for 2011, contributing approximately $10 million to $12 million to EBITDA with the effect on 2011 earnings per share expected to be neutral to slightly accretive, excluding any one-time expenses. In 2012, we anticipate Tasty to contribute approximately $210 million to $225 million to sales with an expected $25 million to $30 million EBITDA contribution and anticipate the transaction to be accretive approximately $.06 to $.09 per diluted share.

“We take a very deliberate approach to selecting acquisitions, focusing on strong brands and premium products that extend our capabilities and geographic reach. We believe Tasty is highly consistent with our acquisition strategy and also offers substantial synergy potential that we expect will generate a strong financial return for our shareholders,” said Deese.

Flowers has experience integrating acquisitions, having completed more than 100 acquisitions since listing publicly in 1968, including 11 in the past decade. Upon the completion of the tender offer and subsequent merger, Flowers and Tasty will work closely to achieve a successful integration and to realize the benefits of the transaction.

About Flowers Foods

Founded in 1919 and headquartered in Thomasville, Ga., Flowers Foods, with $2.6 billion in annual sales, is one of the nation’s leading producers and marketers of packaged bakery foods for retail and foodservice customers. Among the company’s top brands are Nature’s Own, Whitewheat, Cobblestone Mill, Blue Bird, and Mrs. Freshley’s. Flowers operates 39 bakeries that are among the most efficient in the baking industry. Flowers Foods produces, markets, and distributes fresh bakery products that are delivered to customers daily through a direct-store-delivery system serving the Southeast, Mid-Atlantic, and Southwest as well as select markets in California and Nevada. The company also produces and distributes fresh snack cakes and frozen breads and rolls nationally through warehouse distribution. For more information, visit www.flowersfoods.com.

About Tasty Baking Company

Tasty Baking Company (NasdaqGM: TSTY), founded in 1914 and headquartered in Philadelphia, Pa., is one of the country’s leading bakers of snack cakes, pies, cookies, and donuts. The company has manufacturing facilities in Philadelphia and Oxford, Pa. The company offers more than 100 products under the Tastykake brand name. For more information on Tasty Baking Company, visit www.tastykake.com.

Important Information about the Tender Offer

This press release is for informational purposes only and does not constitute an offer to purchase nor a solicitation of an offer to sell any securities of Tasty. Flowers has not commenced the tender offer for the shares of Tasty common stock described in this press release. The solicitation and offer to purchase shares of Tasty common stock will only be made pursuant to a tender offer statement on Schedule TO and related exhibits, including the offer to purchase, letter of transmittal, and other related documents.

Upon commencement of the tender offer, Flowers will file with the SEC a tender offer statement on Schedule TO and related exhibits, including the offer to purchase, letter of transmittal, and other related documents. In addition, Tasty will file with the SEC a tender offer solicitation/recommendation statement on Schedule 14D-9 with respect to the tender offer. These documents will contain important information, including the terms and conditions of the tender offer. Shareholders of Tasty are urged to read each of these documents and any amendments to these documents carefully when they are available prior to making any decisions with respect to the tender offer.

Tasty shareholders will be able to obtain free copies of these materials (when available) and other documents filed with the SEC by Flowers or Tasty through the web site maintained by the SEC at www.sec.gov. In addition, Schedule TO and related exhibits, including the offer to purchase, letter of transmittal, and other related documents may be obtained (when available) for free by contacting Flowers at 1919 Flowers Circle, Thomasville, GA 31757 and the Schedule 14D-9 may be obtained (when available) for free by contacting Tasty at Navy Yard Corporate Center, Three Crescent Drive, Suite 200, Philadelphia, PA 19112.

Forward Looking Statements

Statements contained in this press release that are not historical facts are forward-looking statements. All forward-looking statements are subject to risks and uncertainties that could cause actual results to differ from those projected. Other factors that may cause actual results to differ from the forward-looking statements contained in this release and that may affect the company’s prospects in general include, but are not limited to, (a) competitive conditions in the baked foods industry, including promotional and price competition, (b) changes in consumer demand for our products, (c) the success of productivity improvements and new product introductions, (d) a significant reduction in business with any of our major customers including a reduction from adverse developments in any of our customers’ businesses, (e) fluctuations in commodity pricing, (f) our ability to fully integrate recent acquisitions into our business, (g) our ability to achieve cash flow from capital expenditures and acquisitions and the availability of new acquisitions that build shareholder value, and (h) our ability to successfully consummate the merger transaction. In addition, our results may also be affected by general factors such as economic and business conditions (including the baked foods markets), interest and inflation rates and such other factors as are described in the company’s filings with the Securities and Exchange Commission.

SOURCE Flowers Foods

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China GengSheng Minerals (CHGS) Acquires Minority Interest in Yili Yiqiang Silicon Company

GONGYI, China, April 7, 2011 /PRNewswire-Asia-FirstCall/ — China GengSheng Minerals, Inc. (AMEX:CHGS), a leading China-based high-tech industrial materials manufacturer producing heat resistant, energy efficient materials for a variety of industrial applications, today announced that it has signed an agreement to acquire 24.5% ownership in the Yili Yiqiang Silicon Company (Yili Yiqiang) for RMB 15 million (approximately US$2.3 million). Yili Yiqiang is a manufacturer of green silicon carbide (“SiC”), which is the primary material used in the production of GengSheng’s fine precision abrasive products.

The Company funded this investment through a combination of cash from operations and domestic commercial bank loans. It is expected to close by April 10th, 2011.

“Acquiring a minority stake in Yili Yiqiang enhances our emerging fine precision abrasives products and furthers our strategy to increase our sales and margins in this segments of our business,” said Mr. Shunqing Zhang, China GengSheng’s Chairman and Chief Executive Officer, “With raw material costs high and continuing to rise as a result of tight capacity, our ability to improve the sourcing of high-quality, cost-effective green SiC was crucial to our success in this market. In addition to cost savings, we believe this investment will allow us greater control over the raw material production process, further improving the quality of the green SiC that Yili Yiqiang manufactures.”

Yili Yiqiang, located in Yili, Xinjiang Province in China, one of the region’s leading producers of high-quality green SiC, with average purity of 98.8%. Yili Yiqiang has green SiC reserves of approximately six million metric tons, and current annual production capacity of approximately 16,000 metric tons. Yili Yiqiang expects 2011 revenue of approximately $24 million, based on current production capacity and an average green SiC price of $1,500 per metric ton.

Through this investment, Yili Yiqiang has granted GengSheng right of first refusal on its production output, ensuring consistent, low-cost supply of the principal raw material used in the manufacture of fine precision abrasives.

Mr. Zhang continued, “As one of the safest clean energy technologies, the solar industry is experiencing tremendous growth, which is creating a sizeable market opportunity for fine precision abrasive products. Having launched this product line in third quarter of 2010, we believe that we can grow sales and expand margins by improving overall manufacturing efficiency and continued effective product marketing. With these key objectives in mind and our minority position in Yili Yigiang, we expect that our fine precision abrasives products will contribute to profitability and top-line growth in 2011.”

About China GengSheng Minerals, Inc.

China GengSheng Minerals, Inc. (“GengSheng”) develops, manufactures and markets a broad range of high-tech industrial material products, including monolithic refractories, industrial ceramics, fracture proppants and fine precision abrasives. A market leader offering customized solutions, GengSheng sells its products primarily to the iron and steel industry as heat-resistant components for steel-making furnaces, industrial kilns and other high-temperature vessels to guarantee and improve the productivity of those expensive pieces of equipment, while reducing their consumption of energy. Founded in 1986 and based in China’s Henan province, GengSheng currently has over 200 customers in the iron, steel, oil, glass, cement, aluminum and chemical businesses located in China and other countries. GengSheng conducts business through GengSheng International Corporation, a British Virgin Islands company, and its Chinese subsidiaries, which are Henan GengSheng Refractories Co., Ltd., Zhengzhou Duesail Fracture Proppant Co., Ltd., Henan GengSheng Micronized Powder Materials Co., Ltd, Guizhou SouthEast Prefecture Co., Ltd., GengSheng New Materials Co., Ltd, and Henan GengSheng High Temperature Materials Co., Ltd.

For more information about the Company, please visit http://www.gengsheng.com .

To be added to the Company’s email distribution for future press releases, please send your request to gengsheng@tpg-ir.com.

Safe Harbor Statement

This press release may contain certain forward-looking statements relating to the business of China GengSheng Minerals, Inc., and its subsidiary companies. All statements other than statements of historical fact included herein are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the Companys ability to meet its projected output for the term of the supply contract; the general ability of the Company to achieve its commercial objectives; the business strategy, plans and objectives of the Company and its subsidiaries; and any other statements of non-historical information. These forward-looking statements are often identified by the use of forward-looking terminology such as believes, expects or similar expressions, involve known and unknown risks and uncertainties. Although the Company believes that the expectations reflected in these forward-looking statements are reasonable, they do involve assumptions, risks and uncertainties, and these expectations may prove to be incorrect. Investors should not place undue reliance on these forward-looking statements, which speak only as of the date of this press release. The Companys actual results could differ materially from those anticipated in these forward-looking statements as a result of a variety of factors, including those discussed in the Companys periodic reports that are filed with the Securities and Exchange Commission and available on its website at http://www.sec.gov. All forward-looking statements attributable to the Company or persons acting on its behalf are expressly qualified in their entirety by these factors. Other than as required under the securities laws, the Company does not assume a duty to update these forward-looking statements.

For more information, please contact:

In the US:

The Piacente Group, Inc.

Investor Relations

Brandi Floberg or Lee Roth

Tel: +1-212-481-2050

Email: gengsheng@tpg-ir.com

In China:

The Piacente Group, Inc.

Investor Relations

Wendy Sun

Tel: +86-10-6590-7991

Email: gengsheng@tpg-ir.com

China GengSheng Minerals, Inc.

Investor Relations

Mr. Shuai Zhang

Email: gszs@gengsheng.com

Tel: +86-135-2551-0415

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China Sky One Medical (CSKI) Obtains Production Licenses for Thirteen New Medical Products

HARBIN, China, April 7, 2011 /PRNewswire-Asia-FirstCall/ — China Sky One Medical, Inc. (“China Sky One Medical” or “the Company”) (NASDAQ: CSKI), a leading fully integrated pharmaceutical company in the People’s Republic of China (“PRC”), today announced that the Company, jointly with Heilongjiang Traditional Chinese Medical University (“HTCMU”), has obtained production licenses for thirteen new medical products from the Heilongjiang Food and Drug Administration (“Heilongjiang FDA”) in China. These thirteen products include:

No.

Product Names

1

Kang Xi Eye Patch

2

KangXi Dental Ulcer Membrane

3

KangXi Anti-virus Mouthwash

4

KangXi Dental Ulcer Mouthwash

5

KangXi Snore Stopper

6

Kang Xi Periarthritis Shoulder Patch

7

KangXi Cervical Vertebrae Patch

8

KangXi Lumbar Patch

9

KangXi Rheumatoid Patch

10

KangXi Hyperostosis Patch

11

BiChang Nose Patch

12

YuFu Scar Patch

13

YuFu Wound Healing Patch

China Sky One is preparing for trial production and searching for the best production process for these thirteen products, which the Company expects to introduce to the market as soon as the fourth quarter of 2011.

“We are pleased to obtain production licenses for these exciting new products, which as a group we believe will contribute materially to China Sky One’s revenue and net income in 2012,” commented Mr. Yan-Qing Liu, Chairman and CEO of China Sky One Medical. “As these mostly external-use medical products dovetail well with our existing production facilities and sales network, we expect to manufacture and sell them efficiently without much extra effort. Going forward, we plan to strengthen our partnership with research institutions such as HTCMU, leveraging their R&D capabilities to enrich our product portfolio and improve the Company’s profitability.”

About China Sky One Medical, Inc.

China Sky One Medical, Inc., a Nevada corporation, is a holding company. The Company engages in the manufacturing, marketing and distribution of pharmaceutical, medicinal and diagnostic products. Through its wholly-owned subsidiaries, Harbin Tian Di Ren Medical Science and Technology Company, Harbin First Bio-Engineering Company Limited, Heilongjiang Tianlong Pharmaceutical, Inc. and Peng Lai Jin Chuang Pharmaceutical Company, the Company manufactures and distributes over-the-counter pharmaceutical products, which make up its major revenue source. For more information, visit http://www.cski.com.cn .

Safe Harbor Statement

Certain of the statements made in the press release constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements can be identified by the use of forward- looking terminology such as believe, expect, may, will, should, project, plan, seek, intend, or anticipate or the negative thereof or comparable terminology. Such statements typically involve risks and uncertainties and may include financial projections or information regarding the Companys brand recognition and product quality. Actual results could differ materially from the expectations reflected in such forward-looking statements as a result of a variety of factors, including the risks associated with the effect of changing economic conditions in The Peoples Republic of China, variations in cash flow, reliance on collaborative retail partners and on new product development, variations in new product development, risks associated with rapid technological change, the potential of introduced or undetected flaws and defects in products, consumer acceptance of new products to be launched, including the thirteen new medical products for which the Company received production license approval from Heilongjiang FDA, and other risk factors detailed in reports filed with the Securities and Exchange Commission from time to time.

Investor Relations Contact:

China Sky One Medical

CCG Investor Relations

Hongyu Pan, CFO

Crocker Coulson, President

Email: ir@cski.com.cn

Tel: +1-646-213-1915

Email: crocker.coulson@ccgir.com

Website: www.ccgirasia.com

Mabel Zhang, Vice President

Tel: +1-310-954-1353

Email: mabel.zhang@ccgir.com

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OCZ Technology (OCZ) Now Shipping Vertex 3 Solid State Drive Series

SAN JOSE, Calif., April 7, 2011 (GLOBE NEWSWIRE) — OCZ Technology Group, Inc. (Nasdaq:OCZ), a leading provider of high-performance solid-state drives (SSDs) for computing devices and systems, today announced the availability of the Vertex 3 SATA III SSD Series through the Company’s extensive reseller network. Market availability will vary by region with wider overall availability continuing to ramp in the coming weeks.

“The Vertex 3 series with the SandForce SF-2200 SSD processor has been eagerly anticipated in the marketplace,” said Ryan Petersen, CEO of OCZ Technology Group. “Our partnership with SandForce has again facilitated the introduction of a solution that sets the benchmark for industry leading performance and reliability.”

Recently showcased at the CeBIT tradeshow along with the Vertex 3 Pro, the Vertex 3 is the first available solution to feature the new SandForce SF-2200 SSD processor which harnesses the 6Gbps speed of the SATA III interface to deliver double the performance of the previous generation. The new Vertex 3 raises the bar with up to 550MB/s of bandwidth and up to 60,000 IOPS (4k random write), and is now available in 120GB, 240GB, and 480GB capacities. The enterprise-class Vertex 3 Pro series is expected to begin shipping mid-Q2.

About OCZ Technology Group, Inc.

Founded in 2002, San Jose, CA-based OCZ Technology Group, Inc. (OCZ), is a leader in the design, manufacturing, and distribution of high performance and reliable Solid-State Drives (SSDs) and premium computer components. OCZ has built on its expertise in high-speed memory to become a leader in the SSD market, a technology that competes with traditional rotating magnetic hard disk drives (HDDs). SSDs are faster, more reliable, generate less heat and use significantly less power than the HDDs used in the majority of computers today. In addition to SSD technology, OCZ also offers high performance components for computing devices and systems, including enterprise-class power management products as well as leading-edge computer gaming solutions. For more information, please visit: www.ocztechnology.com.

The OCZ Technology Group, Inc. logo is available at http://www.globenewswire.com/newsroom/prs/?pkgid=7439

Forward-Looking Statements

Certain statements in this press release relate to future events and expectations, including the belief that the transaction will close within 30 days, the expectation that it will accelerate our storage technology innovation, that it will significantly enhance our ability to capitalize on worldwide demand for solid state disk drives, that it will increase customer and stockholder value, that it will expand our reach into embedded markets, that the transaction will become accretive to its earnings per share toward the end of this fiscal year on a non-GAAP basis, excluding acquisition-related expenses, restructuring charges and amortization of intangibles, and, as such constitute forward-looking statements involving known and unknown factors that may cause actual results of OCZ to be different from those expressed or implied in the forward-looking statements. In this context, words such as “will,” “would,” “expect,” “anticipate,” “should” or other similar words and phrases often identify forward-looking statements made on behalf of OCZ. It is important to note that actual results of OCZ may differ materially from those described or implied in such forward-looking statements based on a number of factors and uncertainties, including, but not limited to, the anticipated timing of filings and approvals relating to the acquisition of Indilinx; the satisfaction of other closing conditions; the expected timing of the completion of the acquisition; the ability to successfully integrate the products, services and employees of Indilinx; potential negative impacts from the recent earthquake in Japan; the ability to successfully develop and market new products and services; our ability to maintain other supplier and customer relationships; market acceptance of our products and our ability to continually develop enhanced products; adverse changes both in the general macro-economic environment as well as in the industries we serve, including computer manufacturing, traditional and online retailers, information storage, internet search and content providers and computer system integrators; our ability to efficiently manage material and inventory, including integrated circuit chip costs and freight costs; and our ability to generate cash from operations, secure external funding for our operations and manage our liquidity needs. Other general economic, business and financing conditions and factors are described in more detail in “Item 1A — Risk Factors” in Part I in OCZ’s Annual Report on Form 10-K filed with the SEC on May 20, 2010 and statements made in other subsequent filings. The filings are available both at www.sec.gov as well as via OCZ’s website at www.ocztechnology.com. OCZ does not undertake to update its forward-looking statements.

CONTACT:  OCZ Technology Group, Inc.
          Bonnie Mott, Investor Relations Manager
          408-440-3428
          bmott@ocztechnology.com
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T-DM1 Significantly Improved Progression-Free Survival in Randomized Phase II Trial

T-DM1 Significantly Improved Progression-Free Survival in Randomized Phase II Trial
T-DM1 Significantly Improved Progression-Free Survival in Randomized Phase II Trial

Apr. 7, 2011 (Business Wire) — ImmunoGen, Inc. (Nasdaq: IMGN), a biotechnology company that develops targeted antibody-based anticancer products, today announced that Roche has disclosed positive top-line results from the first randomized trial assessing trastuzumab emtansine (T-DM1, previously known as trastuzumab-DM1) in HER2-positive metastatic breast cancer (MBC). T-DM1 consists of ImmunoGen’s DM1 cancer cell-killing agent attached using the Company’s linker to the HER2-targeting antibody, trastuzumab, developed by Genentech, a member of the Roche Group.

The top-line results disclosed by Roche in a press release today were that patients treated with T-DM1 had a significant improvement in progression-free survival compared with patients treated with Herceptin® (trastuzumab) plus chemotherapy (docetaxel) in the Phase II trial comparing these agents for first-line treatment for HER2-positive MBC.

The detailed findings from this randomized, 137-patient trial are being submitted for presentation at a future medical conference. Favorable preliminary data were reported previously from this trial at the 35th Congress of the European Society of Medical Oncology (ESMO), but progression-free survival data were not available at that time.1

“This top-line information about T-DM1’s performance in the first-line setting is very encouraging and adds to the favorable efficacy and safety data reported across a number of T-DM1 studies. We look forward to learning the detailed data when they are reported at a medical conference,” said Daniel Junius, President and CEO.

About Trastuzumab Emtansine (T-DM1)

Trastuzumab emtansine (the generic or International Non-proprietary Name for T-DM1) utilizes ImmunoGen’s Targeted Antibody Payload (TAP) technology with the trastuzumab antibody developed by Genentech. The compound is in global development by Roche under a collaboration agreement between ImmunoGen and Genentech.

T-DM1 is in Phase III testing for second-line and first-line treatment of HER2-positive MBC. A Phase II trial evaluating the safety of T-DM1 in the neoadjuvant/adjuvant setting began in late 2010.

About ImmunoGen, Inc.

ImmunoGen, Inc. develops targeted anticancer therapeutics using the Company’s expertise in tumor biology, monoclonal antibodies, potent cancer-cell killing agents and engineered linkers. The Company’s TAP technology uses monoclonal antibodies to deliver one of ImmunoGen’s proprietary cancer-cell killing agents specifically to tumor cells. There are currently seven TAP compounds in the clinic, with a wealth of clinical data reported with the technology. ImmunoGen’s collaborative partners include Amgen, Bayer Schering Pharma, Biogen Idec, Biotest, Genentech (a member of the Roche Group), Novartis, and sanofi-aventis. The most advanced compound using ImmunoGen’s TAP technology, trastuzumab emtansine (T-DM1), is in Phase III testing through the Company’s collaboration with Genentech. More information about ImmunoGen can be found at www.immunogen.com.

References

1 Perez E. et al., ESMO 2010, Abstract LBA3

Herceptin® is a registered trademark of Genentech.

This press release includes forward-looking statements. For these statements, ImmunoGen claims the protection of the safe harbor for forward-looking statements provided by the Private Securities Litigation Reform Act of 1995. It should be noted that there are risks and uncertainties related to the development of novel anticancer products, including trastuzumab emtansine (T-DM1), including risks related to uncertainties around clinical studies and data acceptance for presentation, as well as their timings and results. A review of these risks can be found in ImmunoGen’s Annual Report on Form 10-K for the fiscal year ended June 30, 2010 and other reports filed with the Securities and Exchange Commission.

For Investors:

ImmunoGen, Inc.

Carol Hausner, 781-895-0600

Executive Director, Investor Relations and Corporate Communications

info@immunogen.com

or

For Media:

The Yates Network

Barbara Yates, 781-258-6153

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Mad Catz Interactive Inc. (MCZ)

Mad Catz Interactive Inc. primarily develops and markets innovative products for the interactive entertainment industry, the majority of which include markets accessories for videogame systems and PCs under its Mad Catz (casual gaming), Saitek (simulation), Cyborg (pro gaming), Eclipse (home and office) and Tritton (gaming audio) brands.

The Company also operates e-commerce and content websites for videogame and PC products under its GameShark brand, develops, manufactures and markets proprietary earphones under its AirDrives brand, and publishes and distributes video/PC games. Mad Catz’s products are distributed through most of the leading retailers offering interactive entertainment products and has offices in North America, Europe and Asia.

For the last quarter of 2010, the Company reported $93.0 million in net sales, 90.6% higher than the previous year and an all-time record. Mad Catx ended the quarter with $9.9 million of cash, $51.2 million of accounts receivable, $32.5 million of inventories and accounts payable of $55.3 million. According to CEO Darren Richardson, significant improvements to the balance sheet are expected over the next year.

A leader in a dynamic, fast-growing industry that has solid prospects for continuing growth, Mad Catz is currently focused on expanding its product breadth, distribution network and licensing portfolio. The company has growing market share, considerable operating leverage, working capital to fund future growth, and a knowledgeable and skilled management team.

Wednesday, April 6th, 2011 Uncategorized Comments Off on Mad Catz Interactive Inc. (MCZ)

Uroplasty Announces Expanded Insurance Coverage of Posterior Tibial Nerve Stimulation (PTNS)

MINNEAPOLIS, April 5, 2011 /PRNewswire/ — Uroplasty, Inc. (NASDAQ: UPI), a medical device company that develops, manufactures and markets innovative proprietary products to treat voiding dysfunctions, today announced that two private insurance payers have elected to cover posterior tibial nerve stimulation (PTNS) using its Urgent PC Neuromodulation System for the treatment of overactive bladder (OAB) and associated symptoms. Effective April 1, 2011, UnitedHealthcare, a nationwide private insurer, and, effective March 17, 2011, Excellus BlueCross BlueShield (BCBS), a regional insurer in upstate New York, initiated coverage of PTNS.

UnitedHealthcare is the largest single health insurer in the United States covering approximately 33 million lives nationwide. UnitedHealthcare affiliates include AmeriChoice, Great Lakes Health Plan, Health Net of CT, Oxford Health Plans, PacifiCare, Sierra Health and Life, among many others. Excellus BCBS provides health insurance to approximately 1.6 million individuals across upstate New York.

Uroplasty also announced that CIGNA Government Services, the new Medicare carrier for Kentucky effective May 1, 2011, will cover PTNS treatments effective that date. This adds approximately 750,000 lives to the approximately 1.7 million CIGNA covers in Idaho and North Carolina. The addition of Kentucky extends PTNS coverage to approximately 30 million Medicare beneficiaries in 30 states.

“The expansion of PTNS coverage by these leading health insurance providers represents significant progress for our Company,” said David Kaysen, President and CEO of Uroplasty, Inc. “We believe this expanded coverage reflects the strong clinical data that support the efficacy and safety of Urgent PC for the treatment of OAB and associated symptoms. Along with key opinion leaders from the urology field, we continue to meet with other insurers to present the benefits of Urgent PC and anticipate that adoption and coverage of PTNS will continue to grow.”

About Uroplasty, Inc.

Uroplasty, Inc., headquartered in Minnetonka, Minnesota, with wholly-owned subsidiaries in The Netherlands and the United Kingdom, is a medical device company that develops, manufactures and markets innovative proprietary products for the treatment of voiding dysfunctions. Our focus is the continued commercialization of our Urgent PC Neuromodulation System, the only FDA-cleared system that delivers posterior tibial nerve stimulation for the office-based treatment of overactive bladder and associated symptoms of urgency, frequency and urge incontinence. We also offer Macroplastique® Implants, an injectable urethral bulking agent for the treatment of adult female stress urinary incontinence primarily due to intrinsic sphincter deficiency. For more information on the company and its products, please visit Uroplasty, Inc. at www.uroplasty.com.

Forward-Looking Information

This press release contains forward-looking statements that reflect our best estimates regarding future events and financial performance. These forward-looking statements are subject to risks and uncertainties that could cause actual results to differ materially from our anticipated results. We discuss in detail the factors that may affect the achievement of our forward-looking statements in our Annual Report on Form 10-K filed with the SEC. In particular, we cannot be certain that the rate of reimbursement for PTNS treatments will be adequate to justify the cost of our product, that other Medicare carriers or private payers will provide coverage for this treatment, or that any of the other risks identified in our 10-K will not adversely affect our expectations as described in these forward-looking statements.

For Further Information:

Uroplasty, Inc.

David Kaysen, President and CEO, or

Medi Jiwani, Vice President, CFO, Treasurer

952.426.6140

EVC Group

Doug Sherk/Jenifer Kirtland (Investors), 415.896.6820

Chris Gale (Media), 646.201.5431

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VirnetX (VHC) Awarded New Patent, Included in Current Infringement Lawsuits

SCOTTS VALLEY, Calif., April 5, 2011 /PRNewswire/ — VirnetX Holding Corporation (NYSE Amex: VHC), an Internet security software and technology company, today announced that it has been granted U.S. Patent No. 7,921,211, Agile Network Protocol for Secure Communications Using Secure Domain Names, by the U.S. Patent and Trademark Office and has filed papers with the U.S. District Court for the Eastern District of Texas seeking to add allegations that all of the defendants in its two currently-pending patent infringement lawsuits, VirnetX Inc. v. Cisco Systems, Inc., Apple Inc., Aastra USA, Inc., Aastra Technologies Ltd., NEC Corporation, and NEC Corporation of America and VirnetX Inc. v. Mitel Networks Corporation, Mitel Networks, Inc., Siemens Enterprise Communications GmbH & Co. KG, and Siemens Enterprise Communications, Inc. infringe this new patent.

VirnetX also added allegations that Apple’s iPad 2 infringes its patents. VirnetX now accuses the following Apple products of patent infringement: iPhone, iPhone 3G, iPhone 3GS, iPhone 4, iPod Touch, iPad, and iPad 2.

“We are very pleased with the grant of this new patent,” said Kendall Larsen, VirnetX CEO and President. “We believe that it bolsters our patent portfolio and strengthens our current legal activities and licensing efforts.”

About VirnetX

VirnetX Holding Corporation is an internet security software and technology company. The Company’s software and technology solutions, including its secure domain name registry and GABRIEL Connection Technology™, are designed to facilitate secure communications and to create a secure environment for real-time communication applications such as instant messaging, VoIP, smart phones, eReaders and video conferencing. The Company’s patent portfolio includes over 48 U.S. and international patents and pending applications. For more information, please visit www.virnetx.com.

Forward Looking Statement

Statements in this press release that are not statements of historical or current fact constitute “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the Company’s patent portfolio, legal activities and licensing efforts . Such forward-looking statements are based on expectations, estimates and projections about the markets in which the Company operates, management’s beliefs, and certain assumptions made by management and involve known and unknown risks, uncertainties and other unknown factors that could cause the actual results of the Company to be materially different from the historical results or from any future results expressed or implied by such forward-looking statements, including but not limited to (1) the outcome of any legal proceedings that have been or may be initiated by the Company or that may be initiated against the Company; (2) the ability to capitalize on the Company’s patent portfolio and generate licensing fees and revenues; (3) the ability of the Company to be successful in entering into licensing relationships with its targeted customers on commercially acceptable terms; (4) potential challenges to the validity of the Company’s patents underlying its licensing opportunities; (5) the ability of the Company to achieve widespread customer adoption of the Company’s GABRIEL Communication Technology™ and its secure domain name registry; (6) the level of adoption of the 3GPP Series 33 security specifications; and (7) the possibility that Company may be adversely affected by other economic, business, and/or competitive factors. In addition to statements which explicitly describe such risks and uncertainties, readers are urged to consider statements labeled with the terms “believes,” “belief,” “expects,” “intends,” “anticipates,” or “plans” to be uncertain and forward-looking. The forward-looking statements contained herein are also subject generally to other risks and uncertainties that are described from time to time in the Company’s reports and registration statements filed with the Securities and Exchange Commission, including those under the heading “Risk Factors” in Company’s Annual Report on Form 10-K filed with the SEC on March 16, 2011. Many of the factors that will determine the outcome of the subject matter of this press release are beyond the Company’s ability to control or predict. Except as required by law, the Company is under no duty to update any of the forward-looking statements after the date of this press release to conform to actual results.

Contact:

Greg Wood
VirnetX Holding Corporation
831.438.8200
greg_wood@virnetx.com

SOURCE VirnetX Holding Corporation

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Good Times Restaurants Inc. (GTIM) Reports 2nd Quarter Sales Results and New Ad Agency

Apr. 5, 2011 (Business Wire) — Good Times Restaurants Inc. (Nasdaq: GTIM) today announced its eighth consecutive month of same store sales increases with March sales increasing 8.6% from the prior year and that its same store sales for the second quarter of fiscal 2011 increased 5.7%. Year to date for the first six months of the fiscal year same store sales have increased 9.6%.

Commenting on the sales improvement, President & CEO, Boyd Hoback said, “We continue to see results both in an increase in our average check and stable transactions from focusing on our core equity in product quality, including the 2nd quarter promotion of our Fresh Grilled, Honey Cured Bacon products. While we continue to benefit from mild weather this year, it is encouraging that we are achieving sales growth with little to no traditional media support and lower advertising costs. We rolled out Cheese Fries and Loaded Fries in March to leverage our cooked-to-order Fresh Cut Fries and Wild Fries and plan to begin some media support through the spring and summer months with a pipeline of unique product offerings.”

The Company also reported that it has engaged Sukle Advertising & Design in Denver as its agency of record for fiscal 2011 and is working on a refreshed design platform that will come to life in building graphics, packaging, point-of-purchase materials, menu boards and employee uniforms. Hoback added, “We are pleased to be working with Mike Sukle and his team as we refresh and rejuvenate Good Times’ image across all customer touchpoints. Sukle has a reputation for executing big-picture ideas with fresh thinking and innovative designs. We hope to have new menu boards, refreshed building exteriors and new packaging design in place in 2011 to augment a heightened focus on store-level communications and elevating our customers’ experience. Continued compound same store sales growth is our top priority as we work through the uncertain commodity cost environment and continue to explore alternatives for new restaurant growth.”

Sukle Advertising & Design is a Denver-based agency that has been crafting globally recognized, compelling and memorable ideas that create results for clients, such as Noodles & Company, Deep Rock Water, Gates Rubber Corp., Denver Water and many others in a variety of industries.

Good Times is a regional chain of quick service restaurants located primarily in Colorado providing a menu of high-quality all-natural hamburgers, 100% breast of chicken sandwiches, fresh frozen custard, fresh squeezed lemonades and other unique offerings. Good Times currently operates and franchises 49 restaurants.

This press release contains forward looking statements within the meaning of federal securities laws. The words “intend,” “may,” “believe,” “will,” “should,” “anticipate,” “expect,” “seek” and similar expressions are intended to identify forward looking statements. These statements involve known and unknown risks, which may cause Good Times’ actual results to differ materially from results expressed or implied by the forward looking statements. These risks include such factors as the uncertain nature of current restaurant development plans and the ability to implement those plans, delays in developing and opening new restaurants because of weather, local permitting or other reasons, increased competition, cost increases or shortages in raw food products, and other matters discussed under the “Risk Factors” section of Good Times’ Annual Report on Form 10-K for the fiscal year ended September 30, 2009 filed with the SEC. Although Good Times may from time to time voluntarily update its forward looking statements, it disclaims any commitment to do so except as required by securities laws.

Good Times Restaurants Inc.

Investor Relations Contacts:

Boyd E. Hoback, 303-384-1411

President and CEO

or

Christi Pennington, 303-384-1440

Executive Assistant

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Merck to Acquire Inspire Pharmaceuticals, Inc. (ISPH)

Apr. 5, 2011 (Business Wire) — Merck (NYSE:MRK), known as MSD outside the United States and Canada, and Inspire Pharmaceuticals, Inc. (NASDAQ: ISPH) today announced that they have entered into a definitive agreement under which Merck will acquire Inspire, a specialty pharmaceutical company focused on developing and commercializing ophthalmic products.

Under the terms of the agreement, Merck, through a subsidiary, will commence a tender offer for all outstanding common stock of Inspire at a price of $5.00 per share in cash, a 26 percent premium to the closing price of Inspire’s common stock on April 4, 2011. The transaction has a total cash value of approximately $430 million. The transaction has been unanimously approved by the boards of directors of both companies and Inspire’s board recommended that the company’s shareholders tender their shares pursuant to the tender offer. In addition, Warburg Pincus Private Equity IX, L.P., which owns approximately 28 percent of the outstanding shares of Inspire, has agreed to tender all of its shares into the offer.

“Merck continues to build upon its long-term commitment to improving therapeutic options for the treatment of eye diseases,” said Beverly Lybrand, senior vice president and general manager, neuroscience and ophthalmology, Merck. “This acquisition combines the talented commercialization organization at Inspire with the excellent team already in place at Merck thereby strengthening our ophthalmology business and positioning us for future growth with an expanded portfolio. This deal helps address the needs of patients and customers in ophthalmology and creates value for both companies.”

In March, 2011, Merck announced that the New Drug Application (NDA) for SAFLUTAN® (tafluprost), an investigational preservative-free prostaglandin analogue ophthalmic solution, had been accepted for standard review by the U.S. Food and Drug Administration (FDA). SAFLUTAN is the proposed trade name for tafluprost in the United States.

“As one of the world’s leading healthcare companies, Merck is the ideal partner to enhance the long-term potential of Inspire’s portfolio of ophthalmic assets. We are delighted that Merck recognized the strength of an integrated platform leveraging the growing AZASITE® (azithromycin ophthalmic solution) 1% product opportunity and the strong relationships within the ophthalmic community cultivated by our high quality, specialty eye care sales force in the U.S.,” said Adrian Adams, president and CEO of Inspire. “Based upon an extensive analysis of various strategic options, as I have outlined since we announced the results of the TIGER-2 Phase 3 clinical trial, we believe this combination provides a compelling and timely opportunity for our shareholders to realize the value of their investment in Inspire.”

The closing of the tender offer will be subject to certain conditions, including the tender of a number of Inspire shares that, together with shares owned by Merck, represent at least a majority of the total number of Inspire’s outstanding shares (assuming the exercise of all options and vesting of restricted stock units), the expiration of the waiting period under the Hart-Scott-Rodino Antitrust Improvements Act and other customary conditions. Upon the completion of the tender offer, Merck will acquire all remaining shares through a second-step merger.

About AZASITE

Indication: AZASITE® (azithromycin ophthalmic solution) 1% is indicated for the treatment of bacterial conjunctivitis in patients one year and older caused by the following organisms: CDC coryneform group G*, Haemophilus influenzae, Staphylococcus aureus, Streptococcus mitis group, and Streptococcus pneumoniae.

Important Selected Safety Information: AZASITE should not be administered systemically, injected subconjunctivally, or introduced directly into the anterior chamber of the eye. In patients receiving systemically administered azithromycin, serious allergic reactions, including angioedema, anaphylaxis, Stevens Johnson Syndrome and toxic epidermal necrolysis have been reported rarely. Although rare, fatalities have been reported.

As with other anti-infectives, prolonged use may result in overgrowth of non-susceptible organisms, including fungi. If super-infection occurs, discontinue use and institute alternative therapy. Patients should not wear contact lenses if they have signs or symptoms of bacterial conjunctivitis.

Azithromycin should be used during pregnancy only if clearly needed.

The most frequently reported ocular adverse event reported in clinical trials was eye irritation which occurred in 1-2 percent of patients. Other adverse events reported in <1 percent of patients included: ocular reactions (blurred vision, burning, stinging and irritation upon instillation, contact dermatitis, corneal erosion, dry eye, eye pain, itching, ocular discharge, punctate keratitis, visual acuity reduction) and non-ocular reactions (dysgeusia, facial swelling, hives, nasal congestion, periocular swelling, rash, sinusitis, urticaria).

*Efficacy for this organism was studied in fewer than 10 infections.

About Inspire

Inspire is a specialty pharmaceutical company focused on developing and commercializing ophthalmic products. Inspire’s specialty eye care sales force generates revenue from the promotion of AZASITE® (azithromycin ophthalmic solution) 1% for bacterial conjunctivitis. Inspire receives royalties based on net sales of RESTASIS® (cyclosporine ophthalmic emulsion) 0.05% and DIQUAS Ophthalmic Solution 3% (diquafosol tetrasodium) in Japan. For more information, visit www.inspirepharm.com.

About Merck

Today’s Merck is a global healthcare leader working to help the world be well. Merck is known as MSD outside the United States and Canada. Through our prescription medicines, vaccines, biologic therapies, and consumer care and animal health products, we work with customers and operate in more than 140 countries to deliver innovative health solutions. We also demonstrate our commitment to increasing access to healthcare through far-reaching policies, programs and partnerships. For more information, visit www.merck.com.

Inspire Forward-Looking Statement

This news release includes “forward-looking statements” within the meaning of the safe harbor provisions of the United States Private Securities Litigation Reform Act of 1995. The forward-looking statements in this news release relating to management’s expectations and beliefs are based on preliminary information and management assumptions. Specifically, no assurances can be made that the holders of at least a majority of the outstanding shares of Inspire’s common stock will tender their shares pursuant to the tender offer or that the other conditions of the tender offer will be met. Furthermore, no assurances can be made with respect to the strength of Inspire’s integrated platform growing the AZASITE product opportunity.

Such forward-looking statements are subject to a wide range of risks and uncertainties that could cause results to differ in material respects, including those relating to product development, revenue, expense and earnings expectations, the introduction of a generic form of epinastine, intellectual property rights, competitive products, results and timing of clinical trials, success of marketing efforts, the need for additional research and testing, delays in manufacturing, funding, and the timing and content of decisions made by regulatory authorities, including the U.S. Food and Drug Administration. Further information regarding factors that could affect Inspire’s results is included in Inspire’s filings with the SEC. Inspire undertakes no obligation to publicly release the results of any revisions to these forward-looking statements that may be made to reflect events or circumstances after the date hereof.

Merck Forward Looking Statement

This news release includes “forward-looking statements” within the meaning of the safe harbor provisions of the United States Private Securities Litigation Reform Act of 1995. Such statements may include, but are not limited to, statements about the benefits of the merger between Merck and Schering-Plough, including future financial and operating results, the combined company’s plans, objectives, expectations and intentions and other statements that are not historical facts. Such statements are based upon the current beliefs and expectations of Merck’s management and are subject to significant risks and uncertainties. Actual results may differ from those set forth in the forward-looking statements.

The following factors, among others, could cause actual results to differ from those set forth in the forward-looking statements: the possibility that the expected synergies from the merger of Merck and Schering-Plough will not be realized, or will not be realized within the expected time period; the impact of pharmaceutical industry regulation and health care legislation; the risk that the businesses will not be integrated successfully; disruption from the merger making it more difficult to maintain business and operational relationships; Merck’s ability to accurately predict future market conditions; dependence on the effectiveness of Merck’s patents and other protections for innovative products; the risk of new and changing regulation and health policies in the United States and internationally and the exposure to litigation and/or regulatory actions.

Merck undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise. Additional factors that could cause results to differ materially from those described in the forward-looking statements can be found in Merck’s 2010 Annual Report on Form 10-K and the company’s other filings with the Securities and Exchange Commission (SEC) available at the SEC’s Internet site (www.sec.gov).

Important Information about the Tender Offer

The description contained in this press release is neither an offer to purchase nor a solicitation of an offer to sell securities. The planned tender offer described in this press release has not commenced. At the time the planned tender offer is commenced, a tender offer statement on Schedule TO will be filed by Merck with the SEC, and Inspire will file a solicitation/recommendation statement on Schedule 14D-9, with respect to the planned tender offer. The tender offer statement (including an offer to purchase, a related letter of transmittal and other tender offer documents) and the solicitation/recommendation statement will contain important information that should be re ad carefully before making any decision to tender securities in the planned tender offer. Those materials will be made available to Inspire’s stockholders at no expense to them. In addition, all of those materials (and all other tender offer documents filed with the SEC) will be made available at no charge on the SEC’s website at www.sec.gov.

SAFLUTAN® is a registered trademark of Merck, Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. All other brands are trademarks of their respective owners and are not trademarks of Merck & Co., Inc., Whitehouse Station, N.J., USA

Photos/Multimedia Gallery Available: http://www.businesswire.com/cgi-bin/mmg.cgi?eid=6672219&lang=en

Merck

Media:

Ian McConnell

908-423-3046

Investor:

Carol Ferguson or Joe Romanelli

908-423-5088

or

Inspire Pharmaceuticals, Inc.

Media:

Cara Amoroso

919-287-1266

or

Investor:

Jenny Kobin

919-287-1219

Tuesday, April 5th, 2011 Uncategorized Comments Off on Merck to Acquire Inspire Pharmaceuticals, Inc. (ISPH)

ZBB Energy (ZBB) to Provide Energy Storage for Army’s Micro-Grid Project

MILWAUKEE, WI — (Marketwire) — 04/04/11 — ZBB Energy Corporation (NYSE Amex: ZBB), the leading developer of intelligent, renewable energy power platforms, announced today a contract from Eaton Corporation to provide a 500kWH energy storage system for use in a micro-grid application at a U.S. Army facility in Ft. Sill, OK, utilizing ZBB’s next generation ZESS V3 Zinc Bromide flow battery.

The demonstration at Ft. Sill is led by the U.S. Army Engineer Research and Development Center and the Construction Engineering Research Laboratory. This Department of Defense Micro-Grid Development Project will be used to develop standards for the U.S. Army’s effort on the Energy Surety Micro-Grid Program. Research efforts will focus on evaluation of micro-grid technologies to provide off-grid, islanded power to specified areas at Ft. Sill. “We look forward to working with Eaton and the Army to showcase the capabilities of ZBB’s third generation flow battery storage. This application is a great example of how cost effective storage will deliver multiple benefits to the Department of Defense,” said Eric Apfelbach, President & CEO of ZBB Energy.

ZBB’s ZESS V3 technology is a Zinc Bromide flow battery designed to serve as an advanced electrical energy storage device, constructed from environmentally-friendly materials that provide for long service life and advanced performance when compared with traditional chemical batteries.

ZBB will work closely with the Eaton’s Major Projects group and the Eaton Innovation Center’s design team to define operational standards for advanced energy storage systems on micro-grids such as this project and for use at future US DoD facilities.

About ZBB Energy Corporation
ZBB Energy Corporation (NYSE Amex: ZBB) provides advanced electrical power management platforms targeted at the growing global need for distributed renewable energy, energy efficiency, power quality, and grid modernization. ZBB and its power electronics subsidiary, Tier Electronics, LLC have developed a portfolio of intelligent power management platforms that directly integrate multiple renewable and conventional onsite generation sources with rechargeable Zinc Bromide flow batteries and other storage technology. The company also offers advanced systems to directly connect wind and solar equipment to the grid and systems that can form various levels of micro-grids. Tier electronics participates in the energy efficiency markets through their hybrid vehicle control systems, and power quality markets with their line of regulation solutions. Together, these platforms solve a wide range of electrical system challenges in global markets for utility, governmental, commercial, industrial and residential end customers. A developer and manufacturer of its modular, scalable and environmentally friendly power systems (“ZESS POWR™”), ZBB Energy was founded in 1998 and is headquartered in Wisconsin, USA with offices also located in Perth, Western Australia. For more information visit www.zbbenergy.com.

Safe Harbor Statement
Certain statements made in this press contain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities and Exchange Act of 1934, as amended, that are intended to be covered by the “safe harbor” created by those sections. Forward-looking statements, which are based on certain assumptions and describe our future plans, strategies and expectations, can generally be identified by the use of forward-looking terms such as “believe,” “expect,” “may,” “will,” “should,” “could,” “seek,” “intend,” “plan,” “estimate,” “anticipate” or other comparable terms. Forward-looking statements in this press release may address the following subjects among others: statements regarding the sufficiency of our capital resources, expected operating losses, expected revenues, expected expenses and our expectations concerning our business strategy. Forward-looking statements involve inherent risks and uncertainties which could cause actual results to differ materially from those in the forward-looking statements, as a result of various factors including those risks and uncertainties described in the Risk Factors and in Management’s Discussion and Analysis of Financial Condition and Results of Operations sections of our most recently filed Annual Report on Form 10-K and our subsequently filed Quarterly Reports of Form 10-Q. We urge you to consider those risks and uncertainties in evaluating our forward-looking statements. We caution readers not to place undue reliance upon any such forward-looking statements, which speak only as of the date made. Except as otherwise required by the federal securities laws, we disclaim any obligation or undertaking to publicly release any updates or revisions to any forward-looking statement contained herein (or elsewhere) to reflect any change in our expectations with regard thereto or any change in events, conditions or circumstances on which any such statement is based.

Contact Information:
Helen Brown
Investor Relations
ZBB Energy Corporation
T: 262.253.9800

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OncoSec Medical (ONCS) Closes Purchase and License Agreement for Tumor Therapy Technology with Inovio Pharmaceuticals (INO)

SAN DIEGO, April 4, 2011 /PRNewswire/ — OncoSec Medical Incorporated (OTCBB: ONCS), a developer of innovative medical approaches to treat solid tumor cancers with unmet medical needs, announced today that on March 24, 2011 it completed its acquisition of certain assets of Inovio Pharmaceuticals, Inc. (NYSE Amex: INO) and entered into a license agreement with Inovio, pursuant to the terms of an asset purchase agreement with Inovio entered into on March 14, 2011.

OncoSec made an initial payment of $250,000 to Inovio, completing the closing requirements of the purchase and license agreement between the companies. The agreement requires OncoSec to make additional payments of $2.75 million by March 24, 2013, and pay a royalty on commercial product sales. OncoSec has purchased from Inovio certain non-DNA vaccine electroporation technology and intellectual property useful for an electrochemical therapy against solid tumors. OncoSec has also licensed the right to use this electroporation technology to deliver gene-based cytokineimmune therapies for treating solid tumors.

Punit Dhillon, OncoSec’s president and CEO, said: “We are pleased to secure OncoSec’s initial funding announced last week and close the asset purchase and license agreement with Inovio. This transaction marks the official launch of OncoSec’s plan to develop and commercialize this promising technology for the selective treatment of cancerous tumors. With millions of people in the US alone facing detrimental cosmetic, functional and pain outcomes resulting from the invasive treatments used today for various skin and other cancers, there is a clear need for new therapies to address these unmet needs. These electrochemical and gene-based cytokine therapies have previously achieved important clinical outcomes, and we look forward to initiating advanced stage clinical studies by the end of this year.”

OncoSec purchased certain electroporation technology assets and licensed additional electroporation applications based on Inovio’s industry-leading electroporation technology platform that, in addition to DNA vaccines and immune therapeutics, also efficiently delivers chemotherapeutic or gene-based cytokine agents for the treatment of cancerous tumors. When these chemotherapeutic or gene-based cytokine agents are injected into a locally targeted treatment area such as a tumor and the predominantly healthy tissue in the margin surrounding a tumor, they have been shown to selectively and quickly destroy the tumor and cancer cells in the tumor margin. The chemotherapeutic agent acts by directly killing cancerous cells at the delivery site. Gene-based cytokine agents act by inducing broad, non-antigen specific immune responses that have been shown to kill cancerous cells. Initial data has shown that, these therapies may enable heightened concentrations of medicine to be directed to the cancer while reducing overall dosage and moderating or eliminating side effects associated with systemically-applied therapeutic approaches. This optimized delivery is enabled by the local application of brief controlled electrical pulses to cells to temporarily and reversibly increase permeability of the cell membranes in locally targeted tissue, which may dramatically increase cellular uptake of a previously injected agent.

About Inovio Pharmaceuticals, Inc.

Inovio is developing a new generation of vaccines, called DNA vaccines, to treat and prevent cancers and infectious diseases. These SynCon™ vaccines are designed to provide broad cross-strain protection against known as well as newly emergent strains of pathogens such as influenza. These vaccines, in combination with Inovio’s proprietary electroporation delivery devices, have been shown to be safe and generate significant immune responses. Inovio’s clinical programs include three separate programs in Phase II clinical studies, including VGX-3100 for treating cervical dysplasia and cancer. Other Inovio clinical programs include those for avian flu (preventive) and HIV vaccines (both preventive and therapeutic). Inovio is developing universal influenza and other vaccines in collaboration with scientists from the University of Pennsylvania. Other partners and collaborators include Merck, ChronTech, National Cancer Institute, U.S. Military HIV Research Program, NIH, HIV Vaccines Trial Network, University of Southampton, and PATH Malaria Vaccine Initiative. More information is available at www.inovio.com.

About OncoSec Medical Inc.

OncoSec Medical Incorporated (OTC BB: ONCS.OB) is focused on designing, developing and commercializing innovative medical approaches to treat solid tumor cancers with unmet medical needs or where currently approved therapies are inadequate based on their efficacy level or side effect profile. The company’s therapies are based on the use of electroporation delivery in combination with an approved chemotherapeutic drug or a cytokine agent to treat solid tumors. More information is available at www.oncosec.com.

This press release contains forward looking statements within the meaning of the U.S. Private Securities Litigation Reform Act of 1995. Any statements in this release that are not historical facts may be considered such “forward looking statements”, including, among others, statements about the potential effectiveness of our product candidates and the initiation of clinical trials. Forward looking statements are based on management’s current preliminary expectations and are subject to risks and uncertainties which may cause our results to differ materially and adversely from the statements contained herein. Some of the potential risks and uncertainties that could cause actual results to differ from those predicted include: our ability to raise additional funding, our ability to acquire, develop or commercialize new products and product candidates, uncertainties inherent in pre-clinical studies and clinical trials; uncertainties related to regulatory approval of our products and product candidates; unexpected new data, safety and technical issues; and competition and market conditions. These and additional risks and uncertainties are more fully described in OncoSec’s filings with the Securities and Exchange Commission. Undue reliance should not be placed on forward looking statements which speak only as of the date they are made. OncoSec disclaims any obligation to update any forward looking statements to reflect new information, events or circumstances after the date they are made, or to reflect the occurrence of unanticipated events.

SOURCE OncoSec Medical Incorporated

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Orexigen® Therapeutics Presents Additional Contrave® Data from Phase 3 COR-II Trial

NEW ORLEANS, April 4, 2011 /PRNewswire/ — Orexigen® Therapeutics, Inc. (Nasdaq: OREX) announced additional data that showed that overweight and obese patients treated with Contrave® (naltrexone sustained release (SR)/bupropion SR) maintained normal 24-hour circadian patterns over one year of treatment. These data were from the ambulatory blood pressure monitoring (ABPM) sub-study of the COR-II trial that also showed weight loss and improvements in markers of cardiometabolic risk. Data were presented at the 60th Annual Scientific Session of the American College of Cardiology (ACC) taking place in New Orleans.

“The observation that patients in this sub-study maintained normal circadian variation of blood pressure may be particularly relevant since a loss of the nocturnal lowering in blood pressure may predict a poor cardiovascular outcome,” said Jorge Plutzky, M.D., Director of the Vascular Disease Prevention Program at Brigham and Women’s Hospital.

Additional results showed Week 52 weight loss of 7.5% for subjects in the sub-study on Contrave as compared to 2.5% for subjects on placebo (P<0.001) and improvements, at Week 56, in waist circumference (-7.5cm vs. -2.3 cm; P<0.001), hs-CRP (-40.7% vs. -2.4%; P<0.01) and HDL-C (+4.4mg/dL vs. -0.6mg/dL; P<0.01) based on LOCF analyses.

Study Design

The COR-II ABPM sub-study enrolled 182 of the 1496 subjects from the main trial, at nine U.S. sites. Monitoring of ambulatory blood pressure in the sub-study was initiated prior to the intake of study drug and other morning medications and completed approximately 24-hours later at three time points during the study: baseline, Week 24 and Week 52. COR-II is one of the four Phase 3 trials supporting Orexigen’s New Drug Application for Contrave.

About the Contrave Clinical Development Program

All four trials in the COR Phase 3 program (COR-I, COR-II, COR-BMOD and COR-Diabetes) were randomized, double-blind, placebo-controlled trials. The co-primary endpoints were the proportion of patients achieving at least 5% weight loss and percent change in body weight compared to placebo. Secondary endpoints included multiple measures of cardiometabolic risk, quality of life, control of eating, and glycemic control. Contrave was generally well tolerated. The safety and tolerability profile of Contrave in the clinical development program was consistent with the safety profile of the constituent components, which have been in use for other indications for over 20 years. The most frequent treatment-emergent adverse events in patients treated with Contrave were nausea, constipation, headache, vomiting and dizziness. These were mostly mild to moderate in severity, transient, and typically occurred during the first weeks of treatment. The most common adverse events leading to discontinuation with Contrave were nausea, headache, dizziness and vomiting. Treatment with Contrave was not associated with increases in adverse event reports of depression or suicidal ideation compared to placebo. Mean blood pressure with Contrave was generally unchanged from baseline to endpoint. Placebo patients experienced decreases in blood pressure from baseline to endpoint of approximately 2mmHg. Greater weight loss correlated with greater reductions in blood pressure in both Contrave and placebo patients, suggesting that the expected relationship between weight loss and blood pressure was maintained. Importantly, normal circadian blood pressure patterns were preserved with Contrave. There was an increase in pulse of about one beat per minute in patients taking Contrave. Serious events were reported infrequently and included events of cholecystitis (Contrave 0.2%, Placebo <0.1%), seizure (<0.1%, 0%) and major cardiovascular events (<0.1%, <0.1%).

About Orexigen Therapeutics

Orexigen Therapeutics, Inc. is a biopharmaceutical company focused on the treatment of obesity. The Company’s lead product, Contrave, has completed Phase 3 clinical trials and has received a Complete Response Letter from the FDA for its New Drug Application. The company is in the process of determining the next steps for Contrave. The Company’s second product, Empatic™, has completed Phase 2 clinical development. Each product candidate is designed to act on a specific group of neurons in the central nervous system with the goal of achieving appetite suppression and sustained weight loss, through combination therapeutic approaches. Further information about the Company can be found at www.orexigen.com.

Forward-Looking Statements

Orexigen cautions you that statements included in this press release that are not a description of historical facts are forward-looking statements. Words such as “believes,” “anticipates,” “plans,” “expects,” “indicates,” “will,” “intends,” “potential,” “suggests,” “assuming,” “designed” and similar expressions are intended to identify forward-looking statements. These statements are based on the Company’s current beliefs and expectations. These forward-looking statements include statements regarding the potential for, and timing of, approval for Contrave and the loss of the nocturnal lowering in blood pressure may predict a poor cardiovascular outcome. The inclusion of forward-looking statements should not be regarded as a representation by Orexigen that any of its plans will be achieved. Actual results may differ from those set forth in this release due to the risk and uncertainties inherent in the Orexigen business, including, without limitation: Orexigen’s ability to conduct a preapproval cardiovascular outcomes trial, Orexigen’s ability to demonstrate that the risk of major adverse cardiovascular events in overweight and obese subjects treated with Contrave does not adversely affect the product candidate’s benefit-risk profile; the potential for early termination of the collaboration agreement between Orexigen and Takeda; the costs and time required to complete additional clinical, non-clinical or other requirements prior to any resubmission of an NDA; the therapeutic and commercial value of Contrave; Orexigen’s ability to attract and retain key personnel; Orexigen’s ability to maintain sufficient capital; and other risks described in the Company’s filings with the Securities and Exchange Commission. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and Orexigen undertakes no obligation to revise or update this news release to reflect events or circumstances after the date hereof. Further information regarding these and other risks is included under the heading “Risk Factors” in Orexigen’s Quarterly Report on Form 10-K, which was filed with the Securities Exchange Commission on March 11, 2011 and is available from the SEC’s website (www.sec.gov) and on our website (www.orexigen.com) under the heading “Investor Relations”. All forward-looking statements are qualified in their entirety by this cautionary statement. This caution is made under the safe harbor provisions of Section 21E of the Private Securities Litigation Reform Act of 1995.

SOURCE Orexigen Therapeutics, Inc.

Monday, April 4th, 2011 Uncategorized Comments Off on Orexigen® Therapeutics Presents Additional Contrave® Data from Phase 3 COR-II Trial

SmartHeat Inc. Announces Record Full Year 2010 Financial Results – 52% Revenue Growth, 47% Net Income Growth

NEW YORK, March 15, 2011 /PRNewswire-Asia/ — SmartHeat Inc. (Nasdaq: HEAT; website: www.smartheatinc.com), a market leader in China’s clean technology, energy savings industry, today announced record financial results for the year ended December 31, 2010. SmartHeat management is scheduled to host an investor conference call at 8:30 a.m. EDT on March 15, 2011.

Financial Highlights:

  • Revenues of $125.41 million, up 51.89% from 2009
  • Operating income of $26.69 million, up 46.85% from 2009
  • Net income of $22.69 million, up 46.99% from 2009

Business Highlights:

  • Meets or exceeds guidance for 2010
  • Commences acquisition strategy with German heat pump manufacturer and designer GWP in the first quarter of 2011
  • Continues with market expansion in Western China and nuclear industry

Financial Summary:

2010

2009

Change

Revenue

$125,406,862

$82,563,869

51.89%

Gross Profit

$44,711,917

$29,096,064

53.67%

Gross Profit Margin

35.65%

35.24%

Operating Income

$26,691,040

$18,175,199

46.85%

Operating Margin

21.28%

22.01%

Net Income

$22,698,443

$15,442,529

46.99%

Net Margin

18.10%

18.70%

Diluted EPS

$0.68

$0.58

4Q10

4Q09

Change

Revenue

$41,793,612

$26,022,074

60.61%

Gross Profit

$15,276,581

$9,116,632

67.57%

Gross Profit Margin

36.55%

35.03%

Operating Income

$7,850,823

$3,148,012

149.39%

Operating Margin

18.78%

12.10%

Net Income

$6,497,187

$2,923,175

122.26%

Net Margin

15.55%

11.23%

Revenues

In 2010, total sales increased 51.89% to $125.41 million compared to $82.56 million in 2009.

In the fourth quarter of 2010, total sales increased 60.61% to $41.79 million compared to $26.02 million in 4Q09. All three of the Company’s product lines contributed to higher sales in 2010 and were a result of China’s energy-saving policies, continued growth in energy-saving industry, and our successful market expansion.

The breakdown of revenues for 2010 was $55.44 million from PHE units and $60.22 million from heat exchangers, with sales from PHE units up 42.21% compared to 2009 and sales from heat exchangers up 69.18% compared to 2009. Sales from heat meters were up 22.08% from 2009 and accounted for $9.74 million in revenues for 2010.

The breakdown of revenues for the fourth quarter of 2010 was $21.64 million from PHE units and $19.33 million from heat exchangers, with sales from PHE units up 107.57% compared to 4Q09 and sales from heat exchangers up 25.06% compared to 4Q09. Sales from heat meters were up 482.29% from 4Q09 and accounted for $0.83 million in revenues for the quarter.

The following table presents the revenue contribution by percentage for each major product line in 4Q10 in comparison with 4Q09 and fiscal year 2010 in comparison with 2009:

Percent of Total Revenues

Product Line

2010

2009

4Q10

4Q09

Plate Heat Exchange (PHE) Unit

44.21%

47.22%

51.77%

40.06%

Heat Exchanger

48.02%

43.11%

46.25%

59.40%

Heat Meters

7.77%

9.67%

1.98%

0.55%

Total

100.00%

100.00%

100.00%

100.00%

Net Income

Net income in 2010 totaled $22.70 million ($0.68 per diluted share), up 47% from $15.44 million ($0.58 per diluted share) in 2009.

Net income in the fourth quarter totaled $6.50 million, up 122.26% from $2.92 million in 4Q09. The higher net income was driven primarily by increased sales from PHEs and PHE units. Earnings per share for 2010 increased by $0.10 per share.

Gross Profit Margin

Gross profit margin for 2010 was 35.65%, up from 35.24% in 2009. Gross profit margin for 4Q10 was 36.55%, up from 35.03% in 4Q09. The margin maintenance for 2010 is due mainly to our effective cost control and our cost-plus pricing.

Operating Expense

Operating expenses as a percentage of sales were 14.4% for fiscal year 2010 and 17.8% for Q410, compared to 13.2% for fiscal year 2009 and 22.9% for Q409. The increase in operating expenses resulted from increased sales and expansion of our business, including the hiring of more sales personnel, higher depreciation expense, training the marketing team and establishing new sales offices in more regions of China. We believe the expansion and training of our marketing team and other employees will increase sales and improve the efficiency of our operations. We will continue our tight budgetary control and cost effectiveness.

2011 Full Year Guidance

SmartHeat is announcing full year 2011 guidance of $22 – $28 million in net income on $120 – $150 million in revenues, reflecting $0.60 – $0.80 EPS.

Outlook

Mr. James Jun Wang, Chairman and Chief Executive Officer of Smart Heat Inc., commented: “We maintained the momentum from the first nine months of 2010 and delivered another set of strong results. We thank our hard working employees who are dedicated to executing our operational strategy. We are quite pleased to see the significant payback we expected to receive from investments made to expand our sales and distribution channels.”

“Government requirements to implement energy savings and emission reduction have increased the demand for our energy-saving products in all industrial sectors. We are optimistic about taking advantage of economic development in West China and urbanization trends throughout the country even though China is experiencing inflation and is responding to currency and inflationary pressures. Furthermore, we plan to reap the benefits of our expansion into western China and are excited about the addition of the German heat pump manufacturer GWP, which, with our expansion into nuclear energy products, will be a valuable addition to our clean energy business portfolio.” concluded Mr. Wang.

Investor Conference Call Instructions:

SmartHeat management will host an earnings conference call to discuss its 2010 financial results and 2011 outlook.

Date and time: 8:30 a.m. U.S. Eastern Daylight Saving Time, March 15, 2011

U.S. toll free number: +1 866-800-8648

International direct dial-in: +1-617-614-2702

Conference passcode: 163 032 65

About SmartHeat Inc.

Founded by James Jun Wang, a former executive at Honeywell China, SmartHeat Inc. (www.smartheatinc.com) is a NASDAQ Global Market listed (NASDAQ: HEAT) U.S. company with its primary operations in China. SmartHeat is a market leader in China’s clean technology energy savings industry. SmartHeat manufactures heat exchangers, custom plate heat exchanger units (PHE Units) and heat meters. SmartHeat’s products directly address air pollution problems in China where massive coal burning for cooking and heating purposes is the only source of economical heat energy in China. With broad product applications, SmartHeat’s products significantly reduce heating costs, increase energy use, reduce air pollution, and have broad applications. SmartHeat’s customers include global Fortune 500 companies as well as municipalities and industrial/residential users. China’s heat transfer market is currently estimated at approximately $2.4 billion with double-digit annual growth according to the China Heating Association.

Safe Harbor Statement

All statements in this press release that are not historical are forward- looking statements made pursuant to the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. There can be no assurance that actual results will not differ from the company’s expectations. SmartHeat’s actual results may differ from its projections. Further, preliminary results are subject to normal year-end adjustments. You are cautioned not to place undue reliance on any forward-looking statements in this press release as they reflect SmartHeat’s current expectations with respect to future events and are subject to risks and uncertainties that may cause actual results to differ materially from those contemplated. Potential risks and uncertainties include, but are not limited to, the risks described in SmartHeat’s filings with the Securities and Exchange Commission.

Corporate Communications Contact:

Ms. Jane Ai, Corporate Secretary

SmartHeat Inc.

Tel: 011-86-24-25363366

Email: info@SmartHeatinc.com

SMARTHEAT INC. AND SUBSIDIARIES

CONSOLIDATED BALANCE SHEETS

AS OF DECEMBER 31, 2010 AND 2009

2010

2009

ASSETS

CURRENT ASSETS

Cash & cash equivalents

$ 56,806,471

$ 48,967,992

Restricted cash

1,949,742

1,301,573

Accounts receivable, net

47,224,476

31,887,785

Retentions receivable

2,548,401

885,642

Advances to suppliers

8,351,579

7,657,791

Other receivables, prepayments and deposits

6,301,772

3,572,600

Inventories

26,585,362

11,259,273

Deferred tax asset

380,232

Notes receivable – bank acceptances

1,457,457

397,248

Total current assets

151,605,492

105,929,904

NON-CURRENT ASSETS

Deferred tax asset

22,266

Restricted cash

502,672

48,361

Accounts receivable, net

237,384

Retentions receivable

1,062,167

349,931

Intangible assets, net

14,243,734

4,071,021

Construction in progress

81,204

Property and equipment, net

8,381,019

7,739,609

Total noncurrent assets

24,293,062

12,446,306

TOTAL ASSETS

$ 175,898,554

$ 118,376,210

LIABILITIES AND STOCKHOLDERS’ EQUITY

CURRENT LIABILITIES

Accounts payable

$ 4,490,333

$ 3,493,196

Unearned revenue

1,131,193

2,130,637

Taxes payable

2,000,456

2,140,627

Accrued liabilities and other payables

3,039,701

3,685,272

Notes payable – bank acceptances

2,207,280

1,806,564

Loans payable

9,059,749

4,393,544

Total current liabilities

21,928,712

17,649,840

DEFERRED TAX LIABILITY

8,526

COMMITMENTS AND CONTINGENCIES

STOCKHOLDERS’ EQUITY

Common stock, $0.001 par value; 75,000,000
shares authorized, 38,551,939 and 32,794,875
shares issued and outstanding at December 31,
2010 and 2009, respectively

38,552

32,795

Paid in capital

102,251,027

74,917,370

Statutory reserve

5,301,918

2,872,006

Accumulated other comprehensive income

4,252,261

969,988

Retained earnings

41,500,015

21,231,484

Total Company stockholders’ equity

153,343,773

100,023,643

NONCONTROLLING INTEREST

626,069

694,201

TOTAL EQUITY

153,969,842

100,717,844

TOTAL LIABILITIES AND EQUITY

$ 175,898,554

$ 118,376,210

SMARTHEAT INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF INCOME AND COMPREHENSIVE INCOME

FOR THE YEARS ENDED DECEMBER 31, 2010, 2009 AND 2008

2010

2009

2008

Net sales

$ 125,406,862

$ 82,563,869

$ 32,676,082

Cost of goods sold

80,694,945

53,467,805

21,717,735

Gross profit

44,711,917

29,096,064

10,958,347

Operating expenses

Selling expenses

8,559,665

3,934,749

1,564,977

General and administrative expenses

9,461,212

6,986,116

1,851,693

Total operating expenses

18,020,877

10,920,865

3,416,670

Income from operations

26,691,040

18,175,199

7,541,677

Non-operating income (expenses)

Interest income

433,534

409,221

405,266

Interest expense

(131,350)

(518,382)

(314,192)

Financial expense

(49,751)

(30,304)

Exchange gain (loss)

33,932

(26,255)

(12,044)

Other income

201,291

282,393

27,968

Other expenses

(26,954)

(2,838)

(13,709)

Total non-operating income, net

460,702

113,835

93,289

Income before income tax

27,151,742

18,289,034

7,634,966

Income tax expense

4,533,112

2,858,186

1,293,660

Income from operations

22,618,630

15,430,848

6,341,306

Less: Income (loss) attributable to noncontrolling interest

(79,813)

(11,681)

5,966

Income to SmartHeat Inc.

22,698,443

15,442,529

6,335,340

Other comprehensive item

Foreign currency translation gain (loss)

3,282,273

(14,641)

510,770

Comprehensive Income

$ 25,980,716

$ 15,427,888

$ 6,846,110

Basic weighted average shares outstanding

33,419,416

26,535,502

22,176,322

Diluted weighted average shares outstanding

33,453,684

26,592,066

22,176,432

Basic earnings per share

$ 0.68

$ 0.58

$ 0.29

Diluted earnings per share

$ 0.68

$ 0.58

$ 0.29

SMARTHEAT INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CASH FLOWS

FOR THE YEARS ENDED DECEMBER 31, 2010, 2009 AND 2008

2010

2009

2008

CASH FLOWS FROM OPERATING ACTIVITIES:

Income including noncontrolling interest

$ 22,618,630

$ 15,430,848

$ 6,341,306

Adjustments to reconcile income including noncontrolling

interest to net cash used in operating activities:

Depreciation and amortization

1,011,815

635,368

252,598

Unearned interest on accounts receivable

(71,133)

120,522

(127,819)

Stock option compensation expense

195,083

3,292

5,613

Stock issued for consulting service

18,090

Changes in deferred tax

(410,616)

(30,353)

(163)

(Increase) decrease in current assets:

Accounts receivable

(14,716,105)

(20,724,401)

(4,943,868)

Retentions receivable

(2,285,983)

(777,062)

(74,797)

Advances to suppliers

(462,687)

(7,233,127)

62,759

Other receivables, prepayments and deposits

715,988

(2,806,803)

182,577

Inventories

(14,651,940)

(5,143,857)

2,405,678

Increase (decrease) in current liabilities:

Accounts payable

3,634,538

4,051,684

(2,389,649)

Unearned revenue

(1,042,449)

1,278,907

(2,993,636)

Taxes payable

(193,868)

811,275

779,408

Accrued liabilities and other payables

(3,993,197)

(5,776,851)

(261,040)

Net cash used in operating activities

(9,633,834)

(20,160,557)

(761,033)

CASH FLOWS FROM INVESTING ACTIVITIES:

Change in restricted cash

(1,037,592)

(667,502)

(108,040)

Acquisition of property & equipment

(1,112,629)

(942,442)

(439,861)

Acquisition of intangible asset

(10,120,267)

Notes receivable

(495,873)

(14,635)

Cash purchased at acquisition

55,426

Construction in progress

(79,444)

Net cash used in investing activities

(12,845,805)

(1,609,944)

(507,110)

CASH FLOWS FROM FINANCING ACTIVITIES:

Proceeds from short-term loan

4,431,642

4,552,774

5,136,069

Change in due to minority shareholders

(663)

Cash contribution from noncontrolling interest

705,882

Repayment to shareholder

(343,913)

Repayment to short-term loan

(2,605,768)

(7,583,873)

Payment on notes payable

(2,117,001)

Issuance of common stock

27,040,742

65,007,390

5,100,000

Warrants exercised

85,500

1,691,850

Net cash provided by financing activities

29,440,883

69,352,128

2,307,620

EFFECT OF EXCHANGE RATE CHANGE ON CASH & CASH EQUIVALENTS

877,235

(48,847)

2,588

NET INCREASE IN CASH & CASH EQUIVALENTS

7,838,479

47,532,780

1,042,065

CASH & CASH EQUIVALENTS, BEGINNING OF YEAR

48,967,992

1,435,212

393,147

CASH & CASH EQUIVALENTS, END OF YEAR

$ 56,806,471

$ 48,967,992

$ 1,435,212

Supplemental Cash flow data:

Income tax paid

$ 3,738,517

$ 1,500,415

$ 660,127

Interest paid

$ 242,961

$ 338,513

$ 274,969

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Tilman J. Fertitta to Commence Cash Tender Offer for McCormick & Schmick’s (MSSR) Seafood Restaurants

HOUSTON, April 4, 2011 /PRNewswire/ — Tilman J. Fertitta today announced that he intends to commence, through his affiliate LSRI Holdings, Inc., a subsidiary of Landry’s Restaurants, Inc. (collectively, “Landry’s”), an all-cash offer to acquire all of the issued and outstanding shares of common stock of McCormick & Schmick’s Seafood Restaurants, Inc. (Nasdaq: MSSR) (“MSSR”) not already owned by Fertitta or his affiliates for $9.25 per share. The offer will represent an attractive premium of approximately 30% to the closing price of MSSR’s shares on Friday, April 1, 2011. Fertitta already owns directly approximately 10.1% of the outstanding common stock of MSSR, making him one of MSSR’s largest stockholders.

Fertitta remarked, “We believe the offer represents a unique opportunity for MSSR’s stockholders to realize the value of their shares at a significant premium to MSSR’s current and recent stock price.” Full details of the tender offer will be included in Landry’s formal offer to purchase and related materials which will be publicly filed with the Securities and Exchange Commission on Schedule TO and subsequently mailed to MSSR stockholders. Fertitta is requesting a list of MSSR stockholders and expects to mail the formal offer to purchase and related materials to MSSR’s stockholders as soon as possible following receipt of the stockholder list.

Fertitta is fully committed to pursuing this transaction, and has secured a financing commitment from Jefferies Group, Inc. relating to the offer.

The tender offer will be subject to customary conditions, including (i) there being validly tendered and not withdrawn that number of shares of common stock of MSSR, when combined with the shares owned by Fertitta and his affiliates, would represent at least 90% of the total number of then-outstanding shares calculated on a fully diluted basis, (ii) MSSR’s Board of Directors having approved the offer and the potential merger thereafter under Section 203 of the Delaware General Corporation Law or Landry’s being satisfied, in its sole discretion, that Section 203 of the DGCL is inapplicable, (iii) MSSR not having entered into or effectuated any agreement or transaction with any person or entity having the effect of impairing Landry’s ability to acquire MSSR or otherwise diminishing the expected value to Landry’s of the acquisition of MSSR, (iv) Landry’s entering into a definitive agreement regarding the financing commitment to complete the purchase of all of the outstanding shares, and (v) the expiration of the applicable waiting period under the Hart-Scott-Rodino Antitrust Improvements Act of 1976.

Okapi Partners LLC will be the Information Agent for the tender offer and any questions or requests for the offer to purchase and related materials with respect to the tender offer may be directed to 1-877-285-5990 when they become available.

THIS PRESS RELEASE IS FOR INFORMATIONAL PURPOSES ONLY AND IS NOT AN OFFER TO BUY OR THE SOLICITATION OF AN OFFER TO SELL ANY SECURITIES. THE SOLICITATION AND THE OFFER TO BUY MSSR’S COMMON STOCK WILL ONLY BE MADE PURSUANT TO AN OFFER TO PURCHASE AND RELATED MATERIALS THAT LANDRY’S INTENDS TO FILE WITH THE SECURITIES AND EXCHANGE COMMISSION. MSSR STOCKHOLDERS SHOULD READ THESE MATERIALS CAREFULLY WHEN THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION, INCLUDING THE TERMS AND CONDITIONS OF THE OFFER. STOCKHOLDERS WILL BE ABLE TO OBTAIN THE OFFER TO PURCHASE AND RELATED MATERIALS WITH RESPECT TO THE TENDER OFFER FREE AT THE SEC’S WEBSITE AT WWW.SEC.GOV OR FROM LANDRY’S BY CONTACTING OKAPI PARTNERS LLC AT 1-877-285-5990 (TOLL-FREE FROM THE U.S.) WHEN THEY BECOME AVAILABLE.

SOURCE Landry’s Restaurants, Inc.

Monday, April 4th, 2011 Uncategorized Comments Off on Tilman J. Fertitta to Commence Cash Tender Offer for McCormick & Schmick’s (MSSR) Seafood Restaurants

UQM Technologies (UQM) Streamlines its Structure to Focus on Future Growth and Efficiency

Apr. 1, 2011 (Business Wire) — UQM Technologies, Inc. (NYSE Amex: UQM), a developer and manufacturer of power-dense, high-efficiency electric motors, generators and power electronic controllers, is streamlining the company to better prepare for growth and success while improving efficiency.

Previously, UQM operated as two businesses, focused on production and product development. It will now function as one company with efforts aligned into four core functions:

  • Finance – This group will oversee all finances and business functions, including human resources and administration. It will be led by Donald A. French, Treasurer and Chief Financial Officer.
  • Operations – This group will include the manufacturing and procurement functions for all high-volume and prototype systems. It will be led by Ron Burton, Senior Vice President of Operations.
  • Engineering – This group will include both production and development engineering. It will be led by Jon Lutz, Vice President of Engineering.
  • Sales and Business Development – This group will focus on developing new business opportunities, potential market segments, product and regional expansion and investigating potential strategic partnerships. An executive to lead this team will be announced at a later date.

Each leader of these new core areas will report directly to Mr. Ridenour, President and Chief Executive Officer.

“This organizational change is key to our transition to high-volume production of our electric-drive systems and to developing new customers,” said Mr. Ridenour. “This new alignment of resources enables the company to operate more efficiently and helps UQM to focus on the development of next generation products, continue to improve manufacturing processes and reduce cost and more aggressively pursue additional sales of our production-validated electric-propulsion systems.”

Over the past five weeks, UQM has announced business agreements to supply Audi, Rolls-Royce and Saab with electric propulsion systems for pre-production test fleets. The company has a validated production line capacity of 40,000 units per year to supply CODA Automotive and other automotive OEM companies. UQM also supplies Proterra Inc. with electric propulsion systems to power their composite transit buses, as well as Electric Vehicles International (EVI) for its medium-duty delivery vehicles.

“The electrification of the vehicle marketplace is happening at a rapid rate, and our significant investments throughout the company make us well-positioned to deliver the value, innovation and quality that our customers expect,” continued Ridenour. “Our realignment allows us to continue doing what we do, only better – delivering high-quality, competitive products for the fast growing electric vehicle and hybrid markets.”

The company recently relocated to a new 130,000 square foot, 30-acre facility in Longmont, Colorado. The facility houses a fully validated production process that meets Advanced Product Quality Planning (APQP) automotive standards and is capable of high-volume, quality production, including successful programs for major automotive OEMs.

About UQM Technologies, Inc.

UQM Technologies is a developer and manufacturer of power-dense, high-efficiency electric motors, generators and power electronic controllers for the automotive, aerospace, military and industrial markets. A major emphasis for UQM is developing products for the alternative-energy technologies sector, including propulsion systems for electric, hybrid electric, plug-in hybrid electric and fuel cell electric vehicles, under-the-hood power accessories and other vehicle auxiliaries. UQM headquarters, engineering, product development center and manufacturing operation are located in Longmont, Colorado.

Please visit www.uqm.com for more information.

This Release contains statements that constitute “forward-looking statements” within the meaning of Section 27A of the Securities Act and Section 21E of the Securities Exchange Act. These statements appear in a number of places in this Release and include statements regarding our plans, beliefs or current expectations, including those plans, beliefs and expectations of our officers and directors with respect to, among other things, orders to be received under our supply agreement with CODA Automotive, our ability to successfully expand our manufacturing facilities, and the continued growth of the electric-powered vehicle industry. Important Risk Factors that could cause actual results to differ from those contained in the forward-looking statements are contained in our Form 10-Q filed February 1, 2011, which is available through our website at www.uqm.com or at www.sec.gov.

UQM Technologies, Inc.

Donald A. French, 303-682-4918

or

BPC Financial Marketing

John Baldiserra, 800-368-1217

Friday, April 1st, 2011 Uncategorized Comments Off on UQM Technologies (UQM) Streamlines its Structure to Focus on Future Growth and Efficiency

Radio One, Inc. (ROIAK) Announces New Senior Credit Facility

WASHINGTON, April 1, 2011 /PRNewswire/ — Radio One, Inc. (the “Company” or “Radio One”) (Nasdaq: ROIAK; ROIA) today announced that it has closed upon a new senior secured credit facility comprised of a $25.0 million “super-priority” revolving credit facility and a $386.0 million term loan (the “New Senior Credit Facility”). The applicable margin on the New Senior Credit Facility is between (i) 4.50% and 5.50% on the revolving portion of the facility and (ii) 5.00% (with a base rate floor of 2.50% per annum) and 6.00% (with a LIBOR floor of 1.50% per annum) on the term portion of the facility. The revolving portion of the credit facility matures on March 31, 2015 and the term portion of the credit facility matures on March 31, 2016.

(Logo: http://photos.prnewswire.com/prnh/20090806/PH57529LOGO )

As of April 1, 2011, Radio One has initial borrowing availability of $25.0 million under the revolving portion of the credit facility which may be used for general corporate purposes. The proceeds of the term portion of the New Senior Credit Facility were used to refinance all of the Company’s outstanding indebtedness under its prior senior credit facility. Borrowings under the facility are secured by a “super-priority” and/or a first priority lien on substantially all of Radio One’s existing and hereafter acquired assets. Borrowings and availability under the facility are subject to compliance with financial covenants and other terms specified in the agreement.

Additional details regarding the credit facility will be included in a Form 8-K to be filed with the United States Securities and Exchange Commission.

Cautionary Information Regarding Forward-Looking Statements

This press release contains “forward-looking statements” within the meaning of Section 27A of the Securities Act and Section 21E of the Exchange Act. Forward-looking statements represent management’s current expectations and are based upon information available to the Company at the time of this press release. These forward-looking statements involve known and unknown risks, uncertainties and other factors, some of which are beyond the Company’s control, that may cause the actual results to differ materially from any future results, performance or achievements expressed or implied by such forward-looking statements. Important factors that could cause actual results to differ materially are described in the Company’s reports on Forms 10-K, and 10-Q and other filings with the SEC.

Radio One, Inc. (www.radio-one.com) is a diversified media company that primarily targets African-American and urban consumers. The Company is one of the nation’s largest radio broadcasting companies, currently owning 53 broadcast stations located in 16 urban markets in the United States. As a part of its core broadcasting business, Radio One operates syndicated programming including the Russ Parr Morning Show (www.therussparrmorningshow.com) the Yolanda Adams Morning Show (www.syndication1.com/yolanda.htm), the Rickey Smiley Morning Show (www.syndication1.com/rickey.htm), CoCo Brother Live (www.syndication1.com/coco.htm), CoCo Brother’s “Spirit” (www.syndication1.com/coco.htm) program, Bishop T.D. Jakes’ “Empowering Moments” (www.syndication1.com/td.htm), the Reverend Al Sharpton Show (www.syndication1.com/al.htm), and the Warren Ballentine Show (www.syndication1.com/warren.htm). The Company also owns a controlling interest in Reach Media, Inc. (www.blackamericaweb.com), owner of the Tom Joyner Morning Show and other businesses associated with Tom Joyner. Beyond its core radio broadcasting business, Radio One owns Interactive One (www.interactiveone.com), an online platform serving the African-American community through social content, news, information, and entertainment, which operates a number of branded sites, including NewsOne, TheUrbanDaily, HelloBeautiful, and social networks BlackPlanet, MiGente, and AsianAvenue and an interest in TV One, LLC (www.tvoneonline.com), a cable/satellite network programming primarily to African-Americans

SOURCE Radio One, Inc.

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Optimer Pharmaceuticals (OPTR) Reports Inducement Grants Under NASDAQ Listing Rule 5635(c)(4)

SAN DIEGO, April 1, 2011 /PRNewswire/ — Optimer Pharmaceuticals, Inc. (NASDAQ: OPTR) announced today that on March 31, 2011 the Compensation Committee of its Board of Directors approved the grant of inducement stock options to purchase an aggregate of 258,000 shares of common stock to 7 new employees.

(Logo: http://photos.prnewswire.com/prnh/20090413/LA97352LOGO)

Each stock option has an exercise price per share equal to $11.83, the fair market value on the grant date, and vests over four years, with 25% of the shares vesting on the one-year anniversary of the applicable vesting commencement date and 1/48 of the shares vesting monthly thereafter, subject to the new employee’s continued service relationship with the Company. Each stock option also has a ten year term and is subject to the terms and conditions of the Company’s 2006 Equity Incentive Plan and the stock option agreement pursuant to which the option was granted.

The stock options were granted as inducements material to the new employees entering into employment with Optimer in accordance with NASDAQ Listing Rule 5635(c)(4).

About Optimer

Optimer Pharmaceuticals, Inc. is a biopharmaceutical company focused on discovering, developing and commercializing innovative hospital specialty products that have a positive impact on society. Optimer has two anti-infective product candidates in development, fidaxomicin and Pruvel™ (prulifloxacin). Fidaxomicin is a narrow spectrum antibiotic being developed for the treatment of Clostridium difficile infection (CDI). The FDA granted the Company’s request for six-month Priority Review of fidaxomicin, and has assigned a Prescription Drug User Fee Act (PDUFA) goal date of May 30, 2011. The Company also filed a Marketing Authorization Application (MAA) with the European Medicines Agency (EMA) for fidaxomicin. Pruvel™ is a prodrug in the fluoroquinolone class of antibiotics being developed as a treatment for infectious diarrhea. Additional information can be found at http://www.optimerpharma.com.

Contacts

Optimer Pharmaceuticals, Inc.
Christina Donaghy, Corporate Communications Manager
John D. Prunty, Chief Financial Officer & VP Finance
858-909-0736

Canale Communications, Inc.
Jason I. Spark, Senior Vice President
619-849-6005

SOURCE Optimer Pharmaceuticals, Inc.

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U.S. Court Grants LogMeIn’s (LOGM) Motion for Summary Judgment of Non Infringement in Patent Infringement Case

WOBURN, Mass., April 1, 2011 (GLOBE NEWSWIRE) — LogMeIn, Inc. (Nasdaq:LOGM), a provider of SaaS-based, remote-connectivity solutions, today announced that the United States District Court for the Eastern District of Virginia granted LogMeIn’s motion for summary judgment of non infringement in the case brought by 01 Communique. The court indicated a written order will follow. The court indicated it has removed the May 2nd trial from the case calendar.

About LogMeIn, Inc.

LogMeIn (Nasdaq:LOGM) makes it easy to control and access remote devices — desktops, laptops, point-of-sale systems, medical devices, smartphones and more — from any internet-connected computer, including an iPad™, iPhone® and digital displays. Over 11 million active users have connected more than 125 million devices using LogMeIn for business productivity, personal mobility and IT support. LogMeIn is based in Woburn, Massachusetts, USA, with offices in Australia, Hungary, the Netherlands, and the UK.

The LogMeIn, Inc. logo is available at http://www.globenewswire.com/newsroom/prs/?pkgid=6574

This press release contains forward-looking statements with respect to LogMeIn and the patent infringement lawsuit that involve risks and uncertainties. There are a number of important factors that could cause actual results or events to differ materially from those indicated by such forward-looking statements, including uncertainties or difficulties in defending the lawsuit, including the potential of appeal of the granting of the summary judgment motion, as well as other factors described in LogMeIn’s Annual Report on Form 10-K for the year ended December 31, 2010, and its most recent quarterly report filed with the SEC. LogMeIn disclaims any intention or obligation to update any forward-looking statements as a result of developments occurring after the date of this press release.

LogMeIn is a registered trademark of LogMeIn in the U.S. and other countries.

iPhone and iPad are trademarks of Apple, Inc. in the U.S. and other countries around the world.

CONTACT: Media contacts:
         Craig VerColen
         press@logmein.com
         +1-617-599-2180
Friday, April 1st, 2011 Uncategorized Comments Off on U.S. Court Grants LogMeIn’s (LOGM) Motion for Summary Judgment of Non Infringement in Patent Infringement Case