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Drug Highest PhasePhase 2 |
First Approval Ctry. / Loc.- |
First Approval Date- |
一项PT-112联合吉西他滨注射液治疗晚期实体瘤患者的开放性I/II期临床研究
[Translation] An open-label phase I/II clinical study of PT-112 combined with gemcitabine injection in patients with advanced solid tumors
评估PT-112注射液联合吉西他滨注射液治疗晚期实体瘤患者的安全性和耐受性。 估PT-112注射液联合吉西他滨注射液以II期推荐剂量治疗晚期胆道癌患者的抗肿瘤作用。
[Translation] To evaluate the safety and tolerability of PT-112 injection combined with gemcitabine injection in the treatment of patients with advanced solid tumors. To evaluate the anti-tumor effect of PT-112 injection combined with gemcitabine injection at the recommended dose for Phase II in the treatment of patients with advanced biliary tract cancer.
一项PT-112注射液单药治疗晚期实体瘤患者和晚期肝细胞癌患者的开放性I/II期临床研究
[Translation] An open-label phase I/II clinical study of PT-112 injection as a monotherapy in patients with advanced solid tumors and advanced hepatocellular carcinoma
剂量递增阶段 主要目的:评估PT-112注射液治疗晚期实体瘤患者的安全性和耐受性。 剂量确认阶段 主要目的:评估PT-112注射液以推荐最高安全剂量治疗晚期实体瘤患者的安全性和耐受性; II期试验阶段 主要目的:评估PT-112注射液以RP2D剂量治疗晚期肝细胞癌的抗肿瘤作用。
[Translation] Dose escalation phase: Main purpose: to evaluate the safety and tolerability of PT-112 injection in the treatment of patients with advanced solid tumors. Dose confirmation phase: Main purpose: to evaluate the safety and tolerability of PT-112 injection in the treatment of patients with advanced solid tumors at the highest recommended safe dose. Phase II trial phase: Main purpose: to evaluate the anti-tumor effect of PT-112 injection in the treatment of advanced hepatocellular carcinoma at the RP2D dose.
100 Clinical Results associated with SciClone Pharmaceuticals Jiangsu Limited Company
0 Patents (Medical) associated with SciClone Pharmaceuticals Jiangsu Limited Company
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100 Translational Medicine associated with SciClone Pharmaceuticals Jiangsu Limited Company