信達生物(01801.HK)阿達木單抗注射液獲國家藥監局批准兩項新適應症
信達生物(01801.HK)公布,公司自主研發的重組人抗腫瘤壞死因子-α單克隆抗體藥物蘇立信(阿達木單抗注射液)正式獲得國家藥品監督管理局批准兩項新適應症,用於治療兒童斑塊狀銀屑病;及對糖皮質激素應答不充分、需要節制使用糖皮質激素、或不適合進行糖皮質激素治療的成年非感染性中間葡萄膜炎、後葡萄膜炎和全葡萄膜炎。
集團指,蘇立信於今年9月2日首次獲得國家藥品監督管理局上市批准。此前蘇立信已獲批的適應症包括類風濕關節炎、強直性脊柱炎、銀屑病、多關節型幼年特發性關節炎。
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