Monday, December 7, 2009

FDA Grants First Approval for a Product Derived from Pichia pastoris

Dec 7, 2009 - RCT licensee Dyax Corp. has received approval from the U.S. Food and Drug Administration for KALBITOR® (ecallantide) for the treatment of acute attacks of hereditary angioedema (HAE) in patients 16 years of age and older.

The details can be read here.

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