drugset / Trial / NCT06885385

A Phase 2 Study Evaluating the Safety and Efficacy of JS207 With or Without JS015 in Combination With Chemotherapy in Patients With Colorectal Cancer

NCT06885385

Phase 2 Recruiting 60 enrolled Shanghai Junshi Bioscience Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This study is an open label, multicenter Phase II clinical trial aimed at evaluating the safety and efficacy of JS207 with or without JS015 in combination with chemotherapy (XELOX) as a first-line treatment for advanced colorectal cancer with MSS/pMMR. The study was divided into two cohorts: Cohort 1 was JS207 combined with XELOX, and Cohort 2 was JS207 combined with JS015 and XELOX.

Timeline

Start
2025-04-23
Primary completion
2026-11-27
Completion
2027-02-13

Drugs

EvaluationDrugModalityDoseRoute
Subject JS015 Unknown
Subject JS207 Monoclonal antibody
Background Capecitabine Small molecule 1000 mg/m2 Oral
Background Oxaliplatin Small molecule 130 mg/m2 Intravenous

Indications