Industry
Samsung Bioepis submits Remicade biosimilar to U.S. FDA
May 24, 2016
Samsung Bioepis said Tuesday it has submitted SB2, a biosimilar drug referencing Johnson & Johnson’s rheumatoid arthritis treatment Remicade, for review by the U.S. Food and Drug Administration.SB2 is under review for the treatment of rheumatoid arthritis, Crohn’s disease, ulcerative colitis, ankylosing spondylitis, psoriatic arthritis, and psoriasis, the firm said.Samsung Bioepis' R&D center in Songdo, Incheon (Samsung Bioepis)It is Samsung Bioepis’ first biosimilar to seek entry into the U.S.