drugset / Trial / NCT07480733

Phase II Study of JS212/JS213 as Monotherapy and in Combination in Patients With Advanced Malignant Solid Tumors

NCT07480733

Phase 2 Recruiting 410 enrolled Shanghai Junshi Bioscience Co., Ltd.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is a multicenter, open-label Phase II clinical study. The primary objective is to evaluate the investigator-assessed objective response rate of JS212 and JS213 as monotherapy and in combination regimens in patients with advanced solid tumors. This study aims to explore the safety, tolerability, and preliminary efficacy of JS212, JS213, as well as JS212 in combination with JS213, toripalimab, and JS207.

Timeline

Start
2026-04-23
Primary completion
2027-11-30
Completion
2028-11-11

Drugs

EvaluationDrugModalityDoseRoute
Subject JS207 Monoclonal antibody Intravenous
Subject JS212 Unknown Intravenous
Subject JS213 Unknown Intravenous
Subject Toripalimab Monoclonal antibody Intravenous

Indications