Alnylam Submits New Drug Application to FDA Seeking Approval of Givosiran for Acute Hepatic Porphyria
Alnylam Pharmaceuticals has completed its submission of a new drug application (NDA) to the U.S. Food and Drug Administration (FDA), seeking the approval of givosiran for the treatment of acute hepatic porphyria (AHP). Givosiran, also known as ALN-AS1, is an investigational RNA-based therapy designed to…