SOURCE: The Bedford Report

The Bedford Report

March 14, 2011 07:35 ET

Speculative Biotech Firms Grind Through Regulatory Process

The Bedford Report Provides Analyst Research on Advanced Cell Technology & Novavax

NEW YORK, NY--(Marketwire - March 14, 2011) -  There is plenty of optimism surrounding the Biotech industry as firmer pricing and new products have improved sales and earnings trends. Meanwhile, younger, more speculative biotech firms continue to garner significant attention with potential blockbuster drugs working their way through the regulatory process. The Bedford Report examines the outlook for companies in the Biotechnology Industry and provides research reports on Advanced Cell Technology, Inc. (OTCBB: ACTC) and Novavax, Inc. (NASDAQ: NVAX). Access to the full company reports can be found at:

www.bedfordreport.com/2011-03-ACTC

www.bedfordreport.com/2011-03-NVAX

A recent study released by BIO and BioMedTracker claims that the success rate in bringing new medicines to market in the past six years is only about half of what it had been previously. The study claims, however that biotech drugs are twice more likely to gain approval than more traditional chemical drugs.

The study finds that drugs moving from early stage Phase I clinical trials to FDA approval is roughly ten percent, down from around 20 percent in reports involving earlier years.The report adds that approval applications were filed for 55 percent of the drugs that made it to Phase III testing, and 80 percent of those gained eventual approval -- though only half were approved on initial review.

The Bedford Report releases regular market updates on the Healthcare Sector so investors can stay ahead of the crowd and make the best investment decisions to maximize their returns. Take a few minutes to register with us free at www.bedfordreport.com and get exclusive access to our numerous analyst reports and industry newsletters.

Regulatory approval of drugs is a process that frequently comes under fire for being too rapid or too slow. The FDA has reacted to long standing criticism by streamlining some of its guidelines and procedure. Europe's EMEA has largely resisted expediting its approval process. A recent study suggested that the European drug approval system takes twice as long to approve cancer drugs than does the FDA, adding fuel to recent criticism of the European drug approval process.

Last week the European Medicines Agency's Committee for Orphan Medicinal Products granted Advanced Cell Technology a positive decision on its human embryonic stem cell-derived retinal pigment epithelial cells for treatment of a genetic disease that causes progressive vision loss. The opinion now goes to the European Commission, which will determine whether to grant the orphan drug status. The U.S. FDA approved an orphan drug designation for the same product last year.

The Bedford Report provides Analyst Research focused on equities that offer growth opportunities, value, and strong potential return. We strive to provide the most up-to-date market activities. We constantly create research reports and newsletters for our members. The Bedford Report has not been compensated by any of the above-mentioned publicly traded companies. The Bedford Report is compensated by other third party organizations for advertising services. We act as an independent research portal and are aware that all investment entails inherent risks. Please view the full disclaimer at http://www.bedfordreport.com/disclaimer

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