Melanoma patients monitored for Long-Term effects after experimental drug combo
NCT ID NCT06848088
First seen Jun 27, 2026 · Last updated Jul 14, 2026 · Updated 2 times
Summary
This study follows 48 people with advanced melanoma who previously received the experimental drugs fianlimab and cemiplimab in an earlier study. No new treatment is given; instead, researchers track their health, cancer status, and any late side effects over time. The goal is to understand the long-term safety and effectiveness of the drug combination.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 48 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2025
- Expected to finish
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Oct 2029
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Key Inclusion Criteria: 1\. Participants with melanoma who enrolled in cohorts 6, 15, or 16 of study R3767-ONC- 1613 (NCT03005782) Key Exclusion Criteria: None Note: Other protocol-defined Inclusion/ Exclusion criteria may apply
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
11 sites in 2 countries. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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California Pacific Medical Center
San Francisco, California, 94115, United States
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Cancer & Hematology Centers of Western Michigan
Grand Rapids, Michigan, 49546, United States
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Henry Ford Hospital
Detroit, Michigan, 48202, United States
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Rutgers Cancer Institute of New Jersey
New Brunswick, New Jersey, 08901, United States
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Sarah Cannon Research Institute
Nashville, Tennessee, 37203, United States
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South Texas Oncology And Hematology
San Antonio, Texas, 78229, United States
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St. Vincent's University Hospital
Dublin, D04 T6F4, Ireland
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The Angeles Clinic and Research Institute - West Los Angeles Office
Los Angeles, California, 90025, United States
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University of Colorado Anschutz Medical Campus
Aurora, Colorado, 80045, United States
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University of Kansas Hospital
Westwood, Kansas, 66205, United States
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Virginia Cancer Care Specialist, PC
Fairfax, Virginia, 22031, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- New antibody GNR-051 tested for safety in Hard-to-Treat cancers
- Blood test could spot Melanoma's BRAF mutation
- Can a CXCR1/2 blocker boost radiation against cancer that spreads to the brain lining?
- Can a new antibody help the immune system fight Hard-to-Treat tumors?
- Can tumor DNA and immune cells reveal why some cancers resist immunotherapy?
- Can a Two-Drug immune combo shrink melanoma tumors?