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Enrolling by invitation Phase 2 Interventional

A Study to Learn About the Long-Term Health of Adult Participants From a Previous Study of a New Melanoma Treatment

ClinicalTrials.gov ID: NCT06848088

Public ClinicalTrials.gov record NCT06848088. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 12, 2026, 5:37 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Extended Follow-up of Patients With Melanoma Treated With Fianlimab Plus Cemiplimab in Expansion Cohorts From Study R3767-ONC-1613

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT06848088
Recruitment status
Enrolling by invitation
Study type
Interventional
Phase
Phase 2
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
48 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 13, 2025
Primary completion
Oct 9, 2029
Completion
Oct 9, 2029
Last update posted
Jul 12, 2026

2025 – 2029

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
The Angeles Clinic and Research Institute - West Los Angeles Office Los Angeles California 90025
California Pacific Medical Center San Francisco California 94115
University of Colorado Anschutz Medical Campus Aurora Colorado 80045
University of Kansas Hospital Westwood Kansas 66205
Henry Ford Hospital Detroit Michigan 48202
Cancer & Hematology Centers of Western Michigan Grand Rapids Michigan 49546
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08901
Sarah Cannon Research Institute Nashville Tennessee 37203
South Texas Oncology And Hematology San Antonio Texas 78229
Virginia Cancer Care Specialist, PC Fairfax Virginia 22031

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06848088, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 12, 2026 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06848088 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →