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See Latest ArticlesBristol-Myers Squibb Announces Acceptance of Submission for Belatacept Biologic License Application
Bristol Myers-Squibb Company, 09/04/09
Bristol–Myers Squibb Company announced that the U.S. Food and Drug Administration has accepted, for filing and review, the company’s submission of a biologic license application for belatacept, which is in ongoing phase III development for use in kidney transplantation.
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Cell Therapeutics Announces FDAs Oncologic Drugs Advisory Committee to Review Pixantrone for the Treatment of Relapsed/Refractory Aggressive Non-Hodgkins Lymphoma, February 2010
Cell Therapeutics, 12/18/09
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Sanofi-aventis, 12/17/09
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