Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06881537

CapeOX Combined With Bevacizumab Plus Anti-PD1 Antibody as Neoadjuvant Therapy for Locally Recurrent Colorectal Cancer

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
15 (estimated)
Sponsor
Shanghai Changzheng Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This prospective, single-arm study aims to investigate the efficacy and safety of CapeOX combined with Bevacizumab plus Anti-PD1 Antibody as neoadjuvant therapy for locally recurrent colorectal cancer

Conditions

Interventions

TypeNameDescription
DRUGCapecitabineCapecitabine is given orally at 1000mg / m² twice a day from day1-14 every 3 weeks for 4 cycles
DRUGOxaliplatinOxaliplatin is given by intravenous infusion at 130mg / m² on Day 1 every 3 weeks for 4 cycles
DRUGBevacizumabBevacizumab is given intravenously at 7.5mg/kg on day 1 every 3 weeks for 4 cycles
DRUGTislelizumabTislelizumab is given intravenously at 200 mg on day 1 every 3 weeks for 4 cycles

Timeline

Start date
2024-06-01
Primary completion
2025-06-30
Completion
2028-06-30
First posted
2025-03-18
Last updated
2025-03-18

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06881537. Inclusion in this directory is not an endorsement.