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Hyqvia FDA Approval History

FDA Approved: Yes (First approved September 12, 2014)
Brand name: Hyqvia
Generic name: immune globulin and hyaluronidase
Dosage form: Solution for Subcutaneous Administration
Company: Takeda Pharmaceutical Company Limited
Treatment for: Primary Immunodeficiency Syndrome, Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Hyqvia (immune globulin and hyaluronidase) is an immune globulin with a recombinant human hyaluronidase combination used for the treatment of primary immunodeficiency (PI) and chronic inflammatory demyelinating polyneuropathy (CIDP).

Development timeline for Hyqvia

DateArticle
Jan 16, 2024Approval U.S. FDA Approves Takeda’s Hyqvia as Maintenance Therapy in Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
Apr 11, 2023Approval Takeda Receives FDA Approval to Expand the Use of Hyqvia to Treat Primary Immunodeficiency in Children
Sep 12, 2014Approval FDA Approves Baxter’s Hyqvia for Treatment of Adults with Primary Immunodeficiency

Further information

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