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最高研发阶段临床2期 |
首次获批国家/地区- |
首次获批日期- |
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
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。
An Open-Label Phase I/II Clinical Study of PT-112 in Combination With Docetaxel in Subjects With Advanced Solid Tumor in a Phase I Dose Escalation Study and in Subjects With Non-Small Cell Lung Cancer (NSCLC) in a Phase II Dose Confirmation Study
The purpose of this study is to test PT-112 in Combination with Docetaxel in Subjects with Advanced Solid Tumor in a Phase I Dose Escalation Study and in Subjects with Non-Small Cell Lung Cancer.
100 项与 SciClone Pharmaceuticals International (Cayman) Development Limited 相关的临床结果
0 项与 SciClone Pharmaceuticals International (Cayman) Development Limited 相关的专利(医药)
100 项与 SciClone Pharmaceuticals International (Cayman) Development Limited 相关的药物交易
100 项与 SciClone Pharmaceuticals International (Cayman) Development Limited 相关的转化医学