drugset / Trial / NCT07819604

Serplulimab Combined With CAPOX and Bevacizumab as Neoadjuvant Therapy for Locally Advanced Colorectal Cancer

NCT07819604 ↗

Phase 2 Not yet recruiting 85 enrolled Xijing Hospital
NaSingle-groupOpen-labelTreatment

Summary

This is an exploratory study to evaluate the efficacy and safety of neoadjuvant therapy with serplulimab combined with CAPOX and bevacizumab for patients with locally advanced colorectal cancer. The primary endpoint is pathological complete response (pCR). Secondary efficacy endpoints include major pathological response (MPR), R0 resection rate, tumor down-staging, objective response rate (ORR), disease-free survival (DFS), and quality of life, to demonstrate clinical benefit of this combination regimen in the target patient population.

Timeline

Start
2026-09-01
Primary completion
2027-09-01
Completion
2030-09-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody — Intravenous
Subject Capecitabine Small molecule — Intravenous
Subject Oxaliplatin Small molecule — Intravenous
Subject Serplulimab Monoclonal antibody — Intravenous

Indications