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ViroPharma Incorporated (Nasdaq: VPHM) announced that the company submitted a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug Administration (FDA) for Cinryze(TM) C1 Inhibitor (human) as a treatment for acute attacks of hereditary angioedema (HAE). The sBLA is based on a
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Continuous pharmacodynamic activity of eritoran tetrasodium, a tlr4 antagonist, during intermittent intravenous infusion into normal volunteers.
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Arthritis Advisory Committee Recommends FDA Approval of Febuxostat for the Treatment of Hyperuricemia in Patients With Gout
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[news] fda opens office in china to regulate safety of exported drugs

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