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
| Type | Name | Description |
|---|---|---|
| DRUG | Capecitabine | Capecitabine is given orally at 1000mg / m² twice a day from day1-14 every 3 weeks for 4 cycles |
| DRUG | Oxaliplatin | Oxaliplatin is given by intravenous infusion at 130mg / m² on Day 1 every 3 weeks for 4 cycles |
| DRUG | Bevacizumab | Bevacizumab is given intravenously at 7.5mg/kg on day 1 every 3 weeks for 4 cycles |
| DRUG | Tislelizumab | Tislelizumab 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.