Phase II Study of Anti-PD-1/VEGF Bispecific Antibody Ivonescimab in Patients With Previously Treated Metastatic Colorectal Cancer
Part of paid clinical trials in Houston, Texas.
- Sponsor
- M.D. Anderson Cancer Center
- Study ID
- NCT06959550
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Metastatic Colorectal Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Ivonescimab — DRUGGiven by IV
Study Details
The goal of this clinical research study is to learn if ivonescimab can help to control previously treated, metastatic colorectal cancer.
Key Dates
- Start date
- Jul 28, 2025
- Status verified
- May 2026
- Primary completion
- Jul 1, 2028
- Completion
- Jul 1, 2030
Study Design
- Enrollment
- 90 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment with IvonescimabParticipants will be assigned to the study using a Bayesian Optimal Phase 2 (BOP2) design
Primary Outcome Measure
1. Safety and Adverse Events (AEs) [ Time Frame: Through study completion; an average of 1 year ]
Central Contacts
- Saurav Haldar, MD713-792-5111
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The University of Texas M. D. Anderson Cancer Center | Houston | Texas | 77030 | Saurav Haldar, MD (PRINCIPAL_INVESTIGATOR) |
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