drugset / Trial / NCT07503639
Umbrella Trial of Neoadjuvant Therapy for Locally Advanced Colorectal Cancer
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 | — |