Baxter files amended BLA to FDA for HyQvia for primary immunodeficiency
USA-based Baxter International (NYSE: BAX) has completed submission of an amended biologics license application (BLA) to the US Food and Drug Administration to re-initiate the review process for approval of HyQvia (immune globulin infusion 10% [human] with recombinant human hyaluronidase) facilitated subcutaneous infusion for the treatment of adult patients with primary immunodeficiency (PI).
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