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FDA requires longer term trials for HyQvia (Halozyme/Baxter) for Primary Immonodeficiency

Read time: 1 mins
Last updated: 17th Apr 2012
Published: 17th Apr 2012
Source: Pharmawand
The FDA wants additional safety data before it will complete its review of the biologics license application (BLA) for HyQvia, a combination of immune globulin infusion and recombinant human hyaluronidase (rHuPH20) from Halozyme and Baxter under investigation to treat primary immunodeficiency disorder.
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