U.S. FDA Advisory Committee Gives Thumbs Up To Chugai’s Actemra RA Treatment

TOKYO - The U.S. FDA's Arthritis Advisory Committee voted 10 to one for approving Actemra (tocilizumab) a rheumatoid arthritis treatment that Japan's Chugai Pharmaceutical already is marketing for Castleman's disease, Chugai and partner Roche announced July 30