中生製藥(01177.HK)TQB2868注射液獲CDE批准開展III期註冊臨床研究
中國生物製藥(01177.HK)公布,集團開發的1類創新藥TQB2868注射液「PD-1/TGF-β雙功能融合蛋白」聯合鹽酸安羅替尼膠囊和化療用於轉移性胰腺導管腺癌(mPDAC)的一線治療,已在早期臨床試驗中顯示出優異的療效和良好的安全性。
集團近期已向中國國家藥品監督管理局藥品審評中心(CDE)遞交III期臨床溝通,並獲得CDE書面回覆同意開展。
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