China's NMPA accepts Junshi Biosciences' sNDA for toripalimab+bevacizumab combo in first-line HCC treatment.
Shanghai Junshi Biosciences announces that China's National Medical Products Administration (NMPA) accepted its supplemental new drug application (sNDA) for toripalimab (TUOYI®) combined with bevacizumab for the first-line treatment of unresectable or metastatic hepatocellular carcinoma (HCC). Junshi Biosciences is a leading biopharmaceutical company dedicated to novel therapy development.
July 18, 2024
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