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Clinical Trials associated with WJB001 / Enrolling by invitationPhase 1/2 A Phase I/II Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics and Preliminary Efficacy of WJB001 Capsules in Dose Escalation, Dose Expansion, and Efficacy Expansion in Patients With Advanced Solid Tumors
This is a phase I/II study to evaluate the safety and tolerability, DLT(Dose limited toxicity), MTD(Maximum tolerated dose), and RP2D(Recommended phase II dose) of WJB001 capsules in patients with advanced solid tumors, including dose escalation phase, dose expansion phase and cohort expansion phase.The study includes screening, treatment and follow-up periods.
In the Dose Escalation phase:Accelerated titration (the first two dose groups) and "BOIN" combination (the subsequent dose group) were used for dose escalation.
In the Dose Expansion phase:Based on the previous data, 1 to 2 doses were selected to further evaluate the initial efficacy, safety, tolerability and pharmacokinetic characteristics to confirm RP2D.
In the Cohort Expansion phase:The preliminary plan of cohort expansion phase uses the Simon two-stage optimal method to expand 2 to 3 cohorts.
一项评价 WJB001 胶囊在晚期肿瘤患者中口服给药的安全性、耐受性、药代动力学特征及初步疗效的剂量递增、剂量扩展和疗效拓展的 I/II 期临床研究
[Translation] A Phase I/II clinical study to evaluate the safety, tolerability, pharmacokinetic characteristics and preliminary efficacy of oral W**001 capsules in patients with advanced tumors.
评价WJB001治疗特定瘤种如CCNE1过表达或者扩增的子宫浆液性癌和高级别浆液性卵巢癌、输卵管癌或腹膜癌等晚期实体瘤患者的有效性。
[Translation] To evaluate the efficacy of W**001 in treating patients with specific tumor types, such as uterine serous carcinoma and high-grade serous ovarian cancer, fallopian tube cancer, or peritoneal cancer, and other advanced solid tumors with CCNE1 overexpression or amplification.
100 Clinical Results associated with WJB001
100 Translational Medicine associated with WJB001
100 Patents (Medical) associated with WJB001
100 Deals associated with WJB001