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"Samsung Bioepis Co., Ltd. announced on May 24 that the U.S. Food and Drug Administration (FDA) has accepted the review of its Biologics License Application (BLA) for SB2, a biosimilar candidate referencing Remicade® (infliximab), for the treatment of rheumatoid arthritis, Crohn’s disease, ulcerative colitis, ankylosing spondylitis, psoriatic arthritis, and psoriasis.", www.businesskorea.co.kr
"Samsung Group said Tuesday its near-replica of Johnson & Johnson’s blockbuster arthritis drug Remicade has been accepted for review by the U.S. Food and Drug Administration, marking the South Korean conglomerate’s first attempt to sell drugs to Americans, alongside its popular smartphones and televisions.", www.marketwatch.com
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