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Clinical Trials associated with TQB-3558A Phase I, Open-label, Dose Escalation and Expansion Study to Evaluate the Tolerance, Efficacy and Pharmacokinetics of TQB3558 Tablets
This is a study to evaluate the maximum tolerated dose (MTD) , occurrence of all adverse events (AE) and serious adverse events (SAE) , pharmacokinetic parameters and antitumor effect of TQB3558 tablets in Chinese adult patients with advanced solid tumors .The study is divided into phase Ia and phase Ib. Phase Ia: dose escalation period, to evaluate the safety and tolerability of TQB3558 tablets, determine MTD; Phase Ib: effectiveness exploration period, to expand the safe and effective dose group, recommend appropriate dosage and method for subsequent clinical research.
TQB3558片耐受性、有效性和药代动力学Ⅰ期临床试验
[Translation] Phase I clinical trial of tolerability, efficacy and pharmacokinetics of TQB3558 tablets
评价TQB3558片在中国晚期恶性实体瘤成人受试者中的安全性和耐受性,确定最大耐受剂量(MTD)。 评价TQB3558片拓展组的抗肿瘤疗效。 评价TQB3558片在中国晚期恶性实体瘤成人受试者中的药代动力学特征; 评价TQB3558片初步抗肿瘤疗效,为后续临床研究推荐合适的用药剂量和给药方法; 与疗效、作用机制、安全性和/或病理机制相关的生物标志物的研究。 评价TQB3558片安全性;
[Translation] To evaluate the safety and tolerability of TQB3558 tablets in Chinese adult subjects with advanced malignant solid tumors and determine the maximum tolerated dose (MTD). To evaluate the anti-tumor efficacy of the TQB3558 tablets expansion group. To evaluate the pharmacokinetic characteristics of TQB3558 tablets in Chinese adult subjects with advanced malignant solid tumors. To evaluate the preliminary anti-tumor efficacy of TQB3558 tablets and recommend appropriate dosage and administration methods for subsequent clinical studies. To study biomarkers related to efficacy, mechanism of action, safety and/or pathological mechanisms. To evaluate the safety of TQB3558 tablets.
100 Clinical Results associated with TQB-3558
100 Translational Medicine associated with TQB-3558
100 Patents (Medical) associated with TQB-3558
100 Deals associated with TQB-3558