drugset / Trial / NCT04940546

Neoadjuvant Safety of Sintilimab + XELOX + Bevacizumab in PMMR/MSS CRLM Patients

NCT04940546

Phase 1/2 Active not recruiting 36 enrolled Sun Yat-sen University
NaSingle-groupOpen-labelTreatment

Summary

This prospective, single arm study aims to evaluate the preoperative neoadjuvant safety of Sintilimab combined with XELOX plus bevacizumab in colorectal patients with liver metastasis and pMMR/MSS status.

Timeline

Start
2021-06-16
Primary completion
2023-10-30
Completion
2025-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 7.5 mg/kg Intravenous
Subject Capecitabine Small molecule 2 g Oral
Subject Oxaliplatin Small molecule 135 mg/m2 Intravenous
Subject Sintilimab Monoclonal antibody 200 mg Intravenous

Indications