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Clinical Trials associated with TQB3915TQB3915片在晚期恶性实体瘤受试者中的I期临床试验
[Translation] Phase I Clinical Trial of TQB3915 Tablets in Subjects with Advanced Malignant Solid Tumors
1.主要目的:
评估TQB3915片在晚期恶性实体瘤受试者中的安全性和耐受性;
评估TQB3915片联合依维莫司在晚期乳腺癌受试者中的安全性和耐受性。
2.次要目的:
评估TQB3915片在晚期恶性实体瘤受试者中的药代动力学(PK)特征;
评估TQB3915片联合依维莫司在晚期乳腺癌受试者中的药代动力学(PK)特征;
评估TQB3915片单药及联合依维莫司的初步抗肿瘤疗效。
3.探索性目的:
探索TQB3915片治疗相关的生物标志物。
[Translation] 1. Primary purpose:
To evaluate the safety and tolerability of TQB3915 tablets in subjects with advanced malignant solid tumors;
To evaluate the safety and tolerability of TQB3915 tablets combined with everolimus in subjects with advanced breast cancer.
2. Secondary purpose:
To evaluate the pharmacokinetic (PK) characteristics of TQB3915 tablets in subjects with advanced malignant solid tumors;
To evaluate the pharmacokinetic (PK) characteristics of TQB3915 tablets combined with everolimus in subjects with advanced breast cancer;
To evaluate the preliminary anti-tumor efficacy of TQB3915 tablets alone and in combination with everolimus.
3. Exploratory purpose:
To explore biomarkers related to the treatment of TQB3915 tablets.
Phase I Clinical Trial of TQB3915 Tablets in Subjects With Advanced Malignant Solid Tumors
TQB3915 is a selective estrogen receptor covalent antagonist, by covalently binding to estrogen receptor, by changing the conformation of ERα, blocking intracellular signal transmission, thereby inhibiting the growth of tumor cells.
100 Clinical Results associated with TQB3915
100 Translational Medicine associated with TQB3915
100 Patents (Medical) associated with TQB3915
100 Deals associated with TQB3915