FDA Updates Articles
The U.S. Food and Drug Administration has approved a single-use rapid test that detects antibodies to HIV-1 in as little as 60 seconds.
The U.S.Food and Drug Administration has approved a supplemental Biologics License Application to extend the shelf life of Hizentra.
The U.S. Food and Drug Administration (FDA) has approved Benlysta (belimumab) to treat patients with active autoantibody positive lupus (systemic lupus erythematosus) who are receiving standard therapy, including corticosteroids, antimalarials, immunosuppressives and non steroidal anti-inflammatory drugs.