drugset / Trial / NCT06117566

A Study of WX390 Combined With Toripalimab in Patients With Advanced Solid Tumors

NCT06117566

Phase 1/2 Recruiting 100 enrolled Shanghai Jiatan Pharmatech Co., Ltd
Non-randomizedSequentialOpen-labelTreatment

Summary

The goal of this clinical trial is to evaluate the safety and preliminary efficacy of WX390 combined with Toripalimab in patients with advanced solid tumors. The main questions it aims to answer are: * the maximum tolerated dose (MTD) and dose-limiting toxicity (DLT) of WX390; * safety and preliminary in combined therapy. Participants will be treated with WX390 orally and Toripalimab intravenously, and follow the efficacy and safety evaluation according to the protocol.

Timeline

Start
2022-11-18
Primary completion
2025-11-09
Completion
2025-11-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Toripalimab Monoclonal antibody 240 mg Intravenous
Subject WX390 Unknown 0.5 mg Oral
Subject WX390 Unknown 0.7 mg Oral
Subject WX390 Unknown 0.9 mg Oral

Indications