NCT06848088Enrolling by invitationPhase 2
A Study to Learn About the Long-Term Health of Adult Participants From a Previous Study of a New Melanoma Treatment
Extended Follow-up of Patients With Melanoma Treated With Fianlimab Plus Cemiplimab in Expansion Cohorts From Study R3767-ONC-1613
Source: ClinicalTrials.gov · Last updated 13 Jul 2026
Brief summary (registry, in English)
This study is researching the long-term effects of a combination of experimental drugs called fianlimab and cemiplimab. The study is being conducted in patients with advanced skin cancer (melanoma) who had previously been treated with fianlimab and cemiplimab in the study called R3767-ONC-1613 (NCT03005782). The aim of the current study is to see how safe and effective the study drugs are in a long-term follow-up. No study drug will be given during this study. Cancer status will be monitored, in addition to routine care. The study is also collecting information about general health status, and other treatments that may have been received since participation in study R3767-ONC-1613 (NCT03005782).
- Status (registry)
- Enrolling by invitation
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 48 (estimated)
- First submitted
- 24 Feb 2025
- Start date
- 14 Apr 2025
- Primary completion date
- 10 Oct 2029
- Lead sponsor
- Regeneron Pharmaceuticals
- Diseases
- Melanoma
- NCT number
- NCT06848088
- EU CT number
- 2024-517729-20-00
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 48
- From 14 Apr 2025 to the primary completion date, 10 Oct 2029
- 11 sites in 2 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- None
- Note: Other protocol-defined Inclusion/ Exclusion criteria may apply
Who the study is looking for
- 1\. Participants with melanoma who enrolled in cohorts 6, 15, or 16 of study R3767-ONC- 1613 (NCT03005782)
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (11)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| St Vincent's University Hospital Coordinator of this site? Confirm its status | Dublin 4 | Ireland | Not yet recruiting |
| University of Colorado Anschutz Medical Campus Coordinator of this site? Confirm its status | Aurora | United States | Unknown status |
| Henry Ford Hospital Coordinator of this site? Confirm its status | Detroit | United States | Unknown status |
| Virginia Cancer Care Specialist, PC Coordinator of this site? Confirm its status | Fairfax | United States | Unknown status |
| Cancer & Hematology Centers of Western Michigan Coordinator of this site? Confirm its status | Grand Rapids | United States | Unknown status |
| The Angeles Clinic and Research Institute - West Los Angeles Office Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Sarah Cannon Research Institute Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Rutgers Cancer Institute of New Jersey Coordinator of this site? Confirm its status | New Brunswick | United States | Unknown status |
| South Texas Oncology And Hematology Coordinator of this site? Confirm its status | San Antonio | United States | Unknown status |
| California Pacific Medical Center Coordinator of this site? Confirm its status | San Francisco | United States | Unknown status |
| University of Kansas Hospital Coordinator of this site? Confirm its status | Westwood | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.