2013-03-20 13:29:59 -
NEW YORK, NY -- (Marketwire) -- 03/20/13 -- A sharp increase in drug approvals and mergers and acquisitions combined to create a bull market for the Biotechnology Industry in 2012. The iShares NASDAQ Biotechnology Index (IBB), the SPDR S&P Biotech ETF (XBI) and the First Trust Amex Biotechnology Index ETF (FBT) have all gained over 20 percent in the past year, outperforming the broader markets by a good margin. Research Driven Investing examines investing opportunities in the Biotech Industry and provides equity research on Cadence Pharmaceuticals, Inc. (NASDAQ: CADX) and Opexa Therapeutics Inc. (NASDAQ: OPXA).
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www.RDInvesting.com/CADX : ctt.marketwire.com/?release=998662&id=2764465&type=1& ..
www.RDInvesting.com/OPXA : ctt.marketwire.com/?release=998662&id=2764468&type=1& ..
Bloomberg recently reported drug approvals by the U.S. Food and Drug Administration reached a 15 year high in 2012. The FDA approved a total of 39 novel medicines last year, an increase of 30 percent when compared to a year ago. Oncology drugs lead the way with 11 new drugs approved last year. Over the last ten years the number of FDA approvals had averaged roughly 23 a year. The passage of the Prescription Drug User Fee Act (PDUFA) played a major role in the sharp increase in approvals.
The PDUFA "has provided critical resources for improving the quality and timeliness of premarket review of drugs," said FDA spokeswoman Sandy Walsh. "These accomplishments could not have been achieved without the innovations of the biopharmaceutical industry and the dedication and skill of FDA's drug review staff."
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Cadence Pharmaceuticals is a biopharmaceutical company focused on acquiring, in-licensing, developing and commercializing proprietary products principally for use in the hospital setting. U.S. hospitals accounted for approximately $52 billion or 14% of U.S. pharmaceutical sales in 2010, according to independent research firm Wolters Kluwer Pharma Solutions.
Opexa Therapeutics is dedicated to the development of patient-specific cellular therapies for the treatment of autoimmune diseases. The company's lead product candidate Tcelna is a novel T-cell immunotherapy that has been granted Fast Track designation by the U.S. FDA for the Secondary Progressive Multiple Sclerosis (SP-MS) indication.
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