Apex Bioventures Acquisition Corp. Sets Date for Special Meeting of Stockholders to Approve Dissolution

HILLSBOROUGH, Calif., May 7 /PRNewswire-FirstCall/ -- Apex Bioventures Acquisition Corporation (NYSE Amex: PEX ) ("Apex") announced today that a special meeting of stockholders will be held at 10:00 a.m. local time on Tuesday, June 2, 2009, at the offices of Mintz Levin Cohn Ferris Glovsky &...

Medical Community Reacts to Obama and Congressional Plans to Approve Generic Forms of Biologic Medicines

National Press Club Event to Highlight Patient Safety and Discuss Policy Recommendations for Moving Forward WASHINGTON, April 16 /PRNewswire-USNewswire/ -- The Obama administration's goal of expanding the availability of generic forms of biologic drugs - and a variety of congressional effor...

PICA Policyholders Approve ProAssurance Transaction

BIRMINGHAM, Ala. and NASHVILLE, Tenn., March 31 /PRNewswire-FirstCall/ -- ProAssurance Corporation (NYSE: PRA ) announced today that the policyholders of the Podiatry Insurance Company of America (PICA) have overwhelmingly approved the sponsored demutualization that will bring PICA ...

Cellegy and Adamis Stockholders Approve Merger Transaction and Related Proposals

Reverse Split Ratio of Outstanding Cellegy Common Stock Expected to be Approximately 1: 9.929060 BOYERTOWN, Pa., March 24 /PRNewswire-FirstCall/ -- Cellegy Pharmaceuticals, Inc. (OTC Bulletin Board: CLGY) today announced that the stockholders of both Cellegy and Adamis Pharmaceuticals Corpora...

Tepnel Shareholders Approve Acquisition by Gen-Probe

SAN DIEGO, March 16 /PRNewswire-FirstCall/ -- Gen-Probe Incorporated (Nasdaq: GPRO ) announced that shareholders of Tepnel Life Sciences, PLC (AIM: TED) approved the acquisition of Tepnel by Gen-Probe by the requisite majorities at Court and General Meetings held in London earlier today. Mo...

European Commission and United States Food and Drug Administration (FDA) Both Approve New Options for Patients With Certain Primary Brain Tumors

Schering-Plough Receives EU and US Approvals for Intravenous Formulation of Temozolomide As Well As EU Approval for Oral Temozolomide Sachet Presentation KENILWORTH, N.J., March 5 /PRNewswire-FirstCall/ -- Schering-Plough Corporation (NYSE: SGP ) today announced that the European Commission...

Psychoanalysts Approve Position Statement on Homosexuals and Bisexuals Serving in the Military

NEW YORK, Jan. 27 /PRNewswire-USNewswire/ -- Though it's not widely known, psychoanalysts as a professional group are proactive on a number of social issues including homosexuality. During the organization's Winter 2009 Meeting held January 14 - 18 in New York, the American Psychoanalytic A...

Shareholders of Med-Emerg International Inc. approve plan of arrangement with AIM Health Group Inc.

TORONTO, Jan. 8 /PRNewswire-FirstCall/ - Med-Emerg International Inc. (OTCBB:MDER) ("MedEmerg"), one of Canada's leading providers of health services, is pleased to announce that its shareholders have voted in favour of the previously announced plan of arrangement (the "Arrangement") with AIM Heal...

LCA-Vision's Former Executive Management Urge Board of Directors to Immediately Call Special Shareholder Meeting to Approve Poison Pill

CINCINNATI, Dec. 9 /PRNewswire/ -- Dr. Stephen Joffe, Craig Joffe, and Alan Buckey today filed an amendment to their Schedule 13D with the U.S. Securities and Exchange Commission. The group previously filed a 13D disclosing ownership of 11.4% of LCA-Vision, Inc. (Nasdaq: LCAV ), which operates ...

Barr Shareholders Approve Pending Teva Acquisition

MONTVALE, N.J., Nov. 21 /PRNewswire-FirstCall/ -- Barr Pharmaceuticals, Inc. (NYSE: BRL ) today announced that its shareholders overwhelmingly approved the proposals submitted to them relating to the acquisition of Barr by Teva Pharmaceuticals Industries Ltd. (Nasdaq: TEVA ). "Today'...

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OPAXIO(TM) Combined with Alimta(R) Well Tolerated in Dose-Ranging Study of Patients with Advanced Non-Small Cell Lung Cancer

...lease or any other indication, determinations by regulatory, patent and administrative governmental authorities, the possibility that the FDA will not approve a phase III registration strategy for paclitaxel poliglumex if proposed by CTI, CTI's ability to continue to raise capital as needed to fund its opera...

First Potential Lupus-Specific Treatment in Sight

...II clinical study of BENLYSTA. The data from both studies will be evaluated by the U.S. Food and Drug Administration (FDA). Should the FDA ultimately approve BENLYSTA, it would become the first drug successfully developed to specifically treat lupus since the disease was discovered more than a century ago. ...

5-Year Study Published in Diabetologia Demonstrated Long-Term Safety of Lantus(R) Compared to NPH

... clinical data and analysis, including post marketing, decisions by regulatory authorities, such as the FDA or the EMEA, regarding whether and when to approve any drug, device or biological application that may be filed for any such product candidates as well as their decisions regarding labelling and other ...

Sanofi-aventis Stands Behind the Safety of Lantus(R)

... clinical data and analysis, including post marketing, decisions by regulatory authorities, such as the FDA or the EMEA, regarding whether and when to approve any drug, device or biological application that may be filed for any such product candidates as well as their decisions regarding labelling and other ...

Alfacell Provides Shareholder Update

...e company to complete submission of a New Drug Application and if a New Drug Application submission is completed, uncertainty whether FDA will file or approve such application, uncertainties involved in transitioning from concept to product, uncertainties involving the ability of the company to finance resea...

FDA Advisory Committee Votes in Favor of Zyprexa for Two Adolescent Indications

...ew Drug Applications that Lilly submitted for Zyprexa. The FDA takes the advice of its Advisory Committees into consideration when deciding whether to approve new indications, but is not bound by their recommendations. For the proposed schizophrenia indication, the panel voted 11-5, with two abstentions...

Paclitaxel Poliglumex (OPAXIO(TM)) Added to Cisplatin and Radiation Produces 45% Pathologic Complete Remissions in Patients With Esophageal Cancer

...lease or any other indication, determinations by regulatory, patent and administrative governmental authorities, the possibility that the FDA will not approve a phase III registration strategy for paclitaxel poliglumex if proposed by CTI, CTI's ability to continue to raise capital as needed to fund its opera...

NeurogesX Receives FDA Orphan Drug Designation for Qutenza(TM) for Treatment of Postherpetic Neuralgia

...an important economic incentive for the development of new products, providing seven years of exclusive marketing rights during which the FDA will not approve the same drug from another sponsor for the same orphan indication during the exclusivity period. In addition, orphan designation allows for reduction ...

Scientific Data Relating to Cinryze(TM) Presented at 6th Annual C1 Inhibitor Deficiency Workshop

... delay any decision past the time frames anticipated by us, limit any approved indications, deny the approval of Cinryze for acute treatment of HAE or approve a competing product which has been granted orphan drug designation thereby preventing Cinryze from reaching the market for acute treatment of HAE. We ...

Novavax Completes Enrollment of Its Second Phase II Seasonal Influenza VLP Vaccine Clinical Trial

...luenza vaccine or any other vaccine that we may develop; further testing is required before regulatory approval can be applied for and the FDA may not approve a vaccine even if further trial results are similar to those disclosed previously by the company; uncertainties relating to clinical trials; dependenc...

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Dairylands Clinical Information Management

Features:...vides the ancillary departments (Rehabilitation Services, Respiratory Care, and Nutritional Services) with the capability to place and receive orders, approve charges, create work lists and print reports and department logs. Allows for all transcribed documents to be stored within the patients electronic me...
Company:Dairyland Healthcare Solutions

approve in Medical Dictionary

Opiate withdrawal

...l . Dr. David Arneson, NMD. thesourcenmc@msn.com ... hypertensive medication that is commonly utilized in opiate withdrawal syndromes. ... ... approve a new medication for use in the treatment of opiate withdrawal very soon. ... for opiate withdrawal called detox under anesthesia or rapid...

Norplant

... ... Norplant :Levonorgestrel Implants ... Are there any problems when Norplant is put in or taken out? ... 1985 Sweden, Ecuador, and Indonesia approve Norplant . ... Learn about the role that the Norplant implant plays in preventing pregnancy. ... Norplant is a birth control method used by...

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NIH announces new program to develop therapeutics for rare and neglected diseases

...rapy in patients. Clinical trials go through several stages that take several years to determine the safety and efficacy of a new drug. FDA will only approve a drug for general use after it passes these trials. This is also an expensive process, but the failure rate is lower at this stage. "NIH tradition...

New therapeutic strategy could target toxic protein in most patients with Huntington's disease

...as that the number of siRNAs we would have to test in order to have impact on the disease would be too large, and as a consequence the FDA would never approve any trial," he continued. By adding an siRNA against one of two other common SNPs, Zamore says gene silencing could be effective in 75 percent of p...

When fish farms are built along the coast, where does the waste go?

...ccurately predicting where the unhealthy effluent from fish pens will end up, and should probably not be used by state or federal regulators when they approve locations for fish farms. Existing software is typically derived from models that attempt to describe the drift of effluent from sewage outfall pipe...

New standard for popular stevia-based sweetener to assure product's quality

...008, for 90 days. After this comment period, USP's Food Ingredients Expert Committee, which comprises a group of independent, scientific experts, will approve the final monograph to be included in the 2009 FCC supplement. The FCC monograph for Rebaudioside A will contain specifications related to the ing...

Ecological Society of America criticizes administration's overhaul of the Endangered Species Act

... provide little incentive for agencies to assess their work as rigorously as an unbiased reviewer. "What if we allowed pharmaceutical companies to approve and distribute drugs without consulting the Food and Drug Administration?" she asks. "The result would spell potential disaster for humans. In this ca...

UTSA receives $822,000 from Kleberg Foundation to enhance scientific research

...tribute to the Klebergs legacy of philanthropy, said Romo. So, several months ago, we asked the Board of Regents of the University of Texas System to approve the naming of one of our more popular student gathering places outside the new Biotechnology, Sciences and Engineering Building as the Kleberg Commons...

DOE publishes update of plan: 'Facilities for the Future of Science: A 20-Year Outlook'

...s to proceed. Then came a revised proposal in 2004, very positive reviews by scientific leaders in the field worldwide, and DOE decisions in 2005 to approve its mission need and in 2007 to locate the machine at Brookhaven National Laboratory and initiate project engineering and design in fiscal year 2007. ...

Majority of Americans want local action on global warming, says poll

...ing electric utilities to produce at least 20 percent of their electricity from wind, solar and other renewable energy sources. 68 percent would approve changing their city or town zoning rules to decrease suburban sprawl and concentrate new development near the town center. 65 percent would supp...

Americans remain pessimistic about the environment, Stanford-AP survey finds

... percent in 2006). Approval of U.S. businesses' handling of the environment also stayed constant, at 22 percent (21 percent in 2006). ''Republicans approve of U.S. businesses significantly more than do Democrats-31 percent versus 19 percent,'' Krosnick noted. ''This was true in 2006 as well-32 percent ver...

Georgia Tech/Emory Center to study origin of life

...ive research and innovation in the field. The Georgia Tech-Emory grant is Phase I funding; at the end of Phase I in three years, the NSF may choose to approve The Origins Project for Phase II funding, which will provide up to $15 million over five years. The center's research will seek to understand what ...

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Schering-Plough Shareholders Approve Merger With Merck

BOSTON, Aug. 7 /PRNewswire-FirstCall/ -- Schering-Plough Corporation (NYSE: SGP ) announced the voting results of a special shareholders meeting today regarding the proposed merger with Merck & Co., Inc. More than 99 percent of votes cast voted to approve the merger agreement, wit...

TransTech Services Partners, Inc. Shareholders Approve Plan of Liquidation; Company To Distribute Amounts in Trust

NEW YORK, July 10 /PRNewswire-FirstCall/ -- TransTech Services Partners, Inc.("Company") (OTC Bulletin Board: TTSPU, TTSP, TTSPW) today announced that its stockholders voted at its special meeting held on July 8, 2009 to approve the plan of liquidation of the Company. The board of directors...

Modigene Shareholders Approve Company Name Change and Other Proposals at Annual Meeting

-Company's New Name is PROLOR Biotech, Inc.- -Will Now Trade under New Ticker PBTH- -Shareholders Approve Re-Election of Board of Directors and Other Proposals- NES-ZIONA, Israel, June 12 /PRNewswire-FirstCall/ -- Modigene Inc. (OTC Bulletin Board: MODG) today announced that shareho...

Nuvelo Shareholders Approve Issuance of Common Stock Pursuant to Merger Agreement With ARCA biopharma

SAN CARLOS, Calif., Jan. 7 /PRNewswire-FirstCall/ -- Nuvelo, Inc. (Nasdaq: NUVO ) today announced that the stockholders of Nuvelo have approved the issuance of Nuvelo Common Stock pursuant to the merger agreement dated September 24, 2008, as amended, between Nuvelo, ARCA biopharma and a Nuve...

Iomai Stockholders Approve Merger With Intercell Subsidiary

GAITHERSBURG, Md., Aug. 1 /PRNewswire-FirstCall/ -- Iomai Corporation (Nasdaq: IOMI ) announced today that its stockholders approved the merger of Iomai with a wholly-owned subsidiary of Intercell AG. Approximately 71.6 percent of Iomai's outstanding shares entitled to vote at the special mee...

Shareholders Approve All Matters Proposed by Cell Therapeutics, Inc. at Special Meeting in Lieu of Annual Meeting of Shareholders

Proposals approved by more than 95 percent of votes cast SEATTLE, June 20 /PRNewswire-FirstCall/ -- Cell Therapeutics, Inc. (CTI) (Nasdaq: CTIC ; MTA) held a Special Meeting in lieu of the Annual Meeting of Shareholders on Thursday, June 19, 2008 at its headquarters in Seattle. At the...

Results of Court Meeting and Extraordinary General Meeting - Shareholders Approve Scheme of Arrangement and New Share Plans

BASINGSTOKE, England and PHILADELPHIA, May 9 /PRNewswire-FirstCall/ -- Shire plc (LSE: SHP, NASDAQ: SHPGY), the global specialty biopharmaceutical company, announces that ordinary shareholders approved the scheme of arrangement proposed in a circular to shareholders dated 16 April 2008 (the "C...

CardioDynamics Shareholders Approve One-for-Seven Reverse Split of Company's Common Stock and Trading in Post-split Shares Begins May 9, 2008

Split Intended to Maintain Nasdaq Listing and Attract Additional Investors as Company Enters Next Growth Phase SAN DIEGO, May 8 /PRNewswire-FirstCall/ -- CardioDynamics (Nasdaq: CDIC), the innovator and leader of BioZ(R) impedance cardiography (ICG) technology, today announced ...

Renovis Stockholders Approve Acquisition by Evotec

SOUTH SAN FRANCISCO, Calif., May 1 /PRNewswire-FirstCall/ -- Renovis, Inc. (Nasdaq: RNVS ) announced today that its stockholders approved the adoption of the merger agreement with Evotec AG (Frankfurt Stock Exchange: EVT) at a special meeting of stockholders held today. The merger is expected...

VaxGen Stockholders Overwhelmingly Approve Reverse Split Proposal

General Meeting vote suggests broad stockholder support for proposed Raven merger SOUTH SAN FRANCISCO, Calif., Dec. 27 /PRNewswire-FirstCall/ -- VaxGen Inc. (Pink Sheets: VXGN), a biopharmaceutical company, announced today that its stockholders approved the propo...

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Gene

...NA before their proteins can be synthesized. Human gene nomenclature For each known human gene the HUGO Gene Nomenclature Committee (HGNC ) approve a gene name and symbol (short-form abbreviation ). All approved symbols are stored in Genew , the Human Gene Nomenclature Database . Each symbo...

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Somatic cell

...efines somatic cells . ... Drosophila melanogaster Male Somatic Cells Feminized Solely by Tra^sup F&#94 ... new drug regulations approve access to somatic cell therapy)(Brief Article) ... somatic cell ... News archive for somatic cell . ... NewsA five-year ban on somatic ...

Embryo

...and teaching human development. Watch Embryo videos from all over the internet ... How the Body Works: From Embryo to Fetus-Part Two ... HFEA approve human/animal embryo creation for research ... human embryo research and experimentation: all sides to the debate ... Thus, an embryo is viewe...