drugset / Trial / NCT07229586

A Study of SHR-7367 With Anti-tumor Agents in Patients With Solid Tumors

NCT07229586

Phase 1/2 Recruiting 100 enrolled Shanghai Hengrui Pharmaceutical Co., Ltd.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study aims to evaluate the safety and preliminary efficacy of SHR-7367 in combination with antineoplastic agents in subjects with advanced solid tumors, and to determine the maximum tolerated dose (MTD) and the recommended Phase II dose (RP2D).

Timeline

Start
2025-12-02
Primary completion
2027-12
Completion
2027-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Adebrelimab Monoclonal antibody
Subject Gemcitabine Small molecule
Subject Paclitaxel Small molecule
Subject SHR-7367 Unknown

Indications