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A Phase I Study to Evaluate the Safety, Tolerability and Pharmacokinetics of TR128 in Patients With Advanced Solid Tumors
This is a open-label, 3+3 design, dose escalation and expansion, phase I study, to evaluate the safety and tolerability, and to determine the Recommended Phase II Dose (RP2D) of TR128 when administered qd in patients with advanced solid tumors. Up to 5 cohorts of 3-6 patients each will be treated in dose escalation phase of the study. One cycle is 28 days. Dose expansion phase to further evaluate the safety, tolerability and preliminary anti-tumor activity of TR128 at the RP2D.
TR128 治疗晚期实体瘤患者中的安全性、耐受性和药代动力学的Ⅰ期临床试验
评估TR128胶囊单药口服给药在晚期实体瘤患者中的安全性和耐受性,确定剂量限制性毒性(DLT)、最大耐受剂量(MTD)和II期临床试验推荐剂量(RP2D)
A Phase I Clinical Study to Characterize Safety, Tolerability, and Pharmacokinetics of TR115 in Patients With Relapsed / Refractory Non-Hodgkin's Lymphoma or Advanced Solid Tumors
A phase 1 dose escalation and expanded cohort study of TR115 in the treatment of adult patients with relapsed/refractory non-hodgkin's lymphoma or advanced solid tumors.
100 项与 安徽中科拓苒药物科学研究有限公司 相关的临床结果
0 项与 安徽中科拓苒药物科学研究有限公司 相关的专利(医药)
100 项与 安徽中科拓苒药物科学研究有限公司 相关的药物交易
100 项与 安徽中科拓苒药物科学研究有限公司 相关的转化医学