Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05585814

CapeOX Combined With Bevacizumab Plus Anti-PD1 Antibody as Neoadjuvant Therapy for Microsatellite Stable Locally Advanced Rectal Cancer

CapeOX Combined With Bevacizumab Plus Pembrolizumab as Neoadjuvant Therapy for Microsatellite Stable Locally Advanced Rectal Cancer (COBP)

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
30 (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 pembrolizumab plus bevacizumab and chemotherapy as neoadjuvant treatment in pMMR/MSS locally advanced rectal cancer patients

Conditions

Interventions

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

Timeline

Start date
2023-05-01
Primary completion
2024-10-01
Completion
2028-05-01
First posted
2022-10-19
Last updated
2025-03-14

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05585814. Inclusion in this directory is not an endorsement.