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FDA Approves Mavorixafor Capsules to Treat Patients With WHIM Syndrome

The indication is for patients aged 12 years of age and older, and the treatment is intended to increase the number of mature neutrophils and lymphocytes in patients.

FDA Grants Pemivibart Emergency Use Authorization for PrEP of COVID-19 in Immunocompromised Patients

The indication is for adults and adolescents with moderate to severe immune compromise due to medical conditions or immunosuppressive medications and treatments.

FDA Approves Expanded Indication for Hyqvia to Treat Pediatric Primary Immunodeficiency

During the 12-month trial period, Hyqvia was shown to be efficacious treating the occurrence of acute serious bacterial infections in children aged 2 through 16 years with primary immunodeficiency.

Takeda Pharmaceutical Co. Ltd. (TAK) Receives FDA Approval to Expand the Use of HYQVIA

Takeda Receives FDA Approval to Expand the Use of HYQVIA® to Treat Primary Immunodeficiency in Children

HYQVIA® [Immune Globulin Infusion 10% with Recombinant Human Hyaluronidase], the Only Once-a-Month – Every Three or Four Weeks – Subcutaneous Immunoglobulin , is Now Approved for. | April 11, 2023