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A Trial to Learn if Fianlimab and Cemiplimab Are Safe and Work Better Than Anti-PD1 Alone in Adult Participants With Resectable Stage 3 or 4 Melanoma

Active, not recruiting · Phase 2 · NCT06190951

Conditions: Melanoma

At a glance

Research payments reported, 2025
$2.3M
U.S. investigators named
30
Sites paid
29
Planned or actual enrollment
151

About the trial

Sponsor
Regeneron Pharmaceuticals
Tested
cemiplimab (drug), Fixed Dose Combination (FDC) cemiplimab+fianlimab (drug), Placebo (drug)
Dates
Started 2024-09-18; completion 2030-12-09
Results posted
Not yet

This study is researching an experimental drug called REGN3767, also known as fianlimab (R3767), when combined with another medication called cemiplimab (each individually called a "study drug" or called "study drugs" when combined) compared with cemiplimab alone. These types of immunotherapy study drugs are collectively known as immune checkpoint inhibitors. Immunotherapies are treatments that use the immune system to recognize and kill cancer cells. The study is focused on participants with a type of skin cancer known as melanoma. The objective of this study is to see if the combination of fianlimab and cemiplimab is an effective treatment compared to cemiplimab in participants with hig…

From ClinicalTrials.gov, last updated 2026-02-10. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Regeneron Pharmaceuticals, Inc. reported $2.3M in research payments for this study in 2025 (448 payments).

Products named: Libtayo

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.