Equity Research on Gilead Sciences Inc. and Human Genome Sciences Inc. - Regulatory Approval Key for Biotech Companies
(firmenpresse) - NEW YORK, NY -- (Marketwire) -- 10/06/11 -- has a handpicked team of market professionals with over 100 years of combined investing experience. Today they are providing members comprehensive research on the Biotechnology industry and are offering free analytical research on (NASDAQ: GILD) and (NASDAQ: HGSI). Register with us today at to have free access to these research reports.
Drug approvals from administrative bodies in both the U.S. and Europe have been pivotal for biotech companies recently. Investors have been particularly sensitive to decisions made on new drugs considering the state of the global economic recovery. Get your free reports on and at . There is no commitment to join.
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The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency gave a positive recommendation for Eviplera, a combination of Gilead Sciences Inc.'s Truvada and Johnson and Johnson's Edurant, for the treatment of HIV in previously untreated adults. The recommendation bodes very well for European approval when the EMA will make its decision later in the year. report is accessible for free by registering today at .
Human Genome Sciences Inc. has not been as fortunate recently. British regulators chose not to approve the company's lupus drug, Benylsta, for national coverage. The drug had previously seen positive sales in the U.S. though. report is accessible for free by registering today at .
Overall, investors appear particularly sensitive to regulatory decisions on new drugs. Companies receiving approvals could see share prices climb while negative decisions may do just the opposite.
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Datum: 06.10.2011 - 06:15 Uhr
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