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歌禮製藥(01672.HK)治療非酒精性脂肪性肝炎藥物完成首例患者給藥
阿思達克 10-05 08:13
歌禮製藥-B(01672.HK)公布,甲狀腺激素受體β (THRβ)激動劑ASC41用於治療肝穿活檢證實的非酒精性脂肪性肝炎(NASH)患者的52周II期臨床試驗完成首例患者給藥。 ASC41 II期臨床試驗是由中國生物技術公司發起的目前進展最快的療程為52周入組肝穿活檢證實NASH患者的II期臨床試驗。 II期臨床試驗將入組約180名肝穿活檢證實的NASH患者,以1:1:1的比例隨機分配進入兩個藥物組和一個安慰劑對照組,並接受一日一次口服ASC41(2毫克或4毫克)或安慰劑,治療期52周。患者入組預計於2023年第三季完成。
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