Gilead Submits Biologics License Application to U.S. Food and Drug Administration for Bulevirtide, an Investigational Treatment for People Living With Chronic Hepatitis Delta

If Approved, Bulevirtide Will Be the First Treatment Option for Adult Patients in the U. S. With Chronic Hepatitis Delta Virus Infection With Compensated Liver Disease FOSTER CITY, Calif.--(BUSINESS WIRE)--Nov. 19, 2021-- Gilead Sciences, Inc....
Source: Drugs.com - New Drug Applications - Category: Drugs & Pharmacology Source Type: news