News

Wed, 2010-08-25

Pharming Plans Submission Rhucin BLA to US FDA End 2010
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Tue, 2010-07-06

Dyax Announces Marketing Authorization Application for DX-88 (ecallantide) Validated by European Medicines Agency
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Tue, 2010-07-06

Pharming And Sanofi Chimie Sign Manufacturing Agreement For The Drug Substance Of Ruconest
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Thu, 2010-06-24

Pharming Receives Positive Opinion From European Medicines Agency On Rhucin
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Mon, 2010-06-21

ViroPharma Files Prior Approval Supplement (PAS) for Cinryze™ (C1 Esterase Inhibitor [human]) Industrial Scale Manufactoring
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Mon, 2010-06-21

Dyax and Sigma-Tau Announce Partnership to Develop and Commercialize Subcutaneous DX-88 (ecallantide) for Hereditary Angioedema and Other Indications in Europe, North Africa, Middle East and Russia
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