A Study of SHR-7367 With Anti-tumor Agents in Patients With Solid Tumors
A Phase IB/II Clinical Study of the Safety, Tolerability and Efficacy of SHR-7367 in Combination With Anti-tumor Agents in Subjects With Solid Tumors
Shanghai Hengrui Pharmaceutical Co., Ltd.
100 participants
Dec 2, 2025
INTERVENTIONAL
Conditions
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).
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
SHR-7367 injection.
SHR-1316 injection.
Paclitaxel for injection (Albumin Bound).
Gemcitabine Hydrochloride for injection.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07229586