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A Study to Evaluate the Safety and Efficacy of Pumitamig in Combination With Chemotherapy Versus Bevacizumab in Combination With Chemotherapy in Participants With Previously Untreated, Unresectable, or Metastatic Colorectal Cancer
NCT07221357 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the safety and efficacy of pumitamig in combination with chemotherapy versus bevacizumab in combination with chemotherapy in participants with previously untreated, unresectable, or metastatic colorectal cancer
Conditions Studied
Interventions
- DRUG Bevacizumab
- DRUG Pumitamig
- DRUG FOLFIRI
- DRUG FOLFOX
- DRUG CAPOX
Study Locations (20)
California
- Local Institution - 0263 — Los Angeles
- Local Institution - 0345 — Orange
- Local Institution - 0317 — San Francisco
- Local Institution - 0330 — Santa Monica
- Local Institution - 0293 — Stanford
Florida
- Florida Cancer Specialists - East — Cape Coral
- Florida Cancer Specialists - North — St. Petersburg
- Local Institution - 0269 — Tampa
Georgia
- Local Institution - 0276 — Duluth
- Northwest Georgia Oncology Centers, a Service of Wellstar Cobb Hospital — Marietta
Illinois
- Local Institution - 0030 — Chicago
- Local Institution - 0433 — Chicago
Maryland
- Local Institution - 0262 — Baltimore
- Maryland Oncology Hematology - Silver Spring — Silver Spring
Michigan
- Local Institution - 0430 — Ann Arbor
- Local Institution - 0254 — Grand Rapids
Arkansas
- Local Institution - 0432 — Springdale
Iowa
- Local Institution - 0335 — Iowa City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 990 participants |
| Start Date | 2025-12-31 |
| Est. Completion | 2034-03-11 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07221357
The ClinicalTrials.gov registry entry for NCT07221357 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 990 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 504 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Untreated, Unresectable, or Metastatic Colorectal Cancer appearing as the primary indexed condition, and to 5 interventions — of which Bevacizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07221357 reports 20 study locations spanning 10 distinct geographic areas — top geographies include California, Florida, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07221357 about?
NCT07221357 is a clinical study titled "A Study to Evaluate the Safety and Efficacy of Pumitamig in Combination With Chemotherapy Versus Bevacizumab in Combination With Chemotherapy in Participants With Previously Untreated, Unresectable, or Metastatic Colorectal Cancer". The purpose of this study is to evaluate the safety and efficacy of pumitamig in combination with chemotherapy versus bevacizumab in combination with chemotherapy in participants with previously untreated, unresectable, or metastatic colorectal cancer
What is the current status of trial NCT07221357?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 990 participants. The study started on 2025-12-31. Estimated completion is 2034-03-11.
What conditions does trial NCT07221357 study?
This clinical trial studies the following conditions: Untreated, Unresectable, or Metastatic Colorectal Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07221357?
The interventions under investigation include: Bevacizumab (DRUG), Pumitamig (DRUG), FOLFIRI (DRUG), FOLFOX (DRUG), CAPOX (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07221357?
This trial is sponsored by Bristol-Myers Squibb, which has 504 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07221357 being conducted?
This trial has 20 study locations across Arkansas, California, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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