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
| Type | Name | Description |
|---|---|---|
| DRUG | Capecitabine | Capecitabine is given orally at 1000mg / m² twice a day from day1-14 every 3 weeks for 3 cycles |
| DRUG | Oxaliplatin | Oxaliplatin is given by intravenous infusion at 130mg / m2 on Day 1 every 3 weeks for 3cycles |
| DRUG | Bevacizumab | Bevacizumab is given intravenously at 7.5mg/kg on day 1 every 3 weeks for 3 cycles |
| DRUG | Pembrolizumab | Pembrolizumab 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.