Real-world Outcomes Among Patients With Melanoma Treated With Neoadjuvant Nivolumab+Relatlimab or Nivolumab+Ipilimumab
Part of paid clinical trials in Dublin, Ohio.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT07091695
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Nivolumab + relatlimab — BIOLOGICALAs prescribed by the treating clinician
- Nivolumab + ipilimumab — BIOLOGICALAs prescribed by the treating clinician
Study Details
The purpose of this study is to understand the characteristics of adults diagnosed with with clinically palpable stage III resectable melanoma, the associated treatment patterns for their disease, and outcomes associated with the real-world use of neoadjuvant nivolumab+relatlimab or nivolumab+ipilimumab
Key Dates
- Start date
- May 11, 2025
- Status verified
- Nov 2025
- Primary completion
- Nov 6, 2025
- Completion
- Nov 6, 2025
Study Design
- Enrollment
- 100 participants (actual)
Arms
- Arm: Participants receiving nivolumab + relatlimab treatment
- Arm: Participants receiving nivolumab + ipilimumab treatment
Primary Outcome Measure
Participant baseline demographics [ Time Frame: Baseline ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Cardinal Health | Dublin | Ohio | 43017 | - |
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