drugset / Trial / NCT07503639

Umbrella Trial of Neoadjuvant Therapy for Locally Advanced Colorectal Cancer

NCT07503639

Phase 2 Not yet recruiting 134 enrolled Fudan University
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a prospective, open-label, single-center, phase II umbrella trial designed to evaluate the efficacy and safety of neoadjuvant therapy for locally advanced colorectal cancer. Patients will be stratified into four cohorts based on microsatellite instability (MSI) status, KRAS mutation status, and the consensus molecular subtypes (CMS). Six arms are included across four cohorts and each arm will be assigned to a specific treatment regimen. The primary endpoint is the complete response rate. Secondary endpoints include safety, organ preservation rate (for rectal cancer only), R0 resection rate, surgical complications, treatment compliance, 3-year survival, and quality of life (QoL) score.

Timeline

Start
2026-04
Primary completion
2028-04
Completion
2030-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 1000 mg/m2
Subject Cetuximab β Monoclonal antibody 500 mg/m2
Subject HRS-4642 Unknown 1200 mg
Subject HRS-7058 Unknown 200 mg
Subject Oxaliplatin Small molecule 130 mg/m2
Subject Retlirafusp alfa Protein / enzyme biologic 1800 mg
Subject SHR-8068 Monoclonal antibody 280 mg

Indications