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Takeda’s Gammagard Liquid Wins FDA Approval in CIDP

Follows recent FDA approval of HYQVIA in adults with chronic inflammatory demyelinating polyneuropathy (CIDP).

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By: Kristin Brooks

Managing Editor, Contract Pharma

Takeda received approval from the U.S. FDA for GAMMAGARD LIQUID [Immune Globulin Infusion (Human) 10% solution] as an intravenous immunoglobulin (IVIG) therapy to improve neuromuscular disability and impairment in adults with chronic inflammatory demyelinating polyneuropathy (CIDP). It can be used as induction therapy, which includes an induction dose followed by maintenance doses.  This milestone follows the recent FDA approval of HYQVIA [Immune Globulin Infusion 10% (Human) with Recombinant...

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