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Study identifier: NCT06581406 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Randomized, Phase 2/3 Study to Investigate the Efficacy and Safety of RP2 in Combination With Nivolumab in Immune Checkpoint Inhibitor-Naïve Adult Patients With Metastatic Uveal Melanoma

Condition: Metastatic Uveal Melanoma  ·  Sponsor: Replimune, Inc.

PhasePhase 2/Phase 3
Planned participants280
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to measure the clinical benefits of the combination of RP2 and nivolumab as compared with the combination of nivolumab and ipilimumab in patients with metastatic uveal melanoma who have not been treated with immune checkpoint inhibitor therapy.

This description comes directly from the study's public registry record.

Talk to the study team

Clinical Trials at Replimune  ·  1-781-222-9570  ·  Clinicaltrials@replimune.com

Giuseppe Gullo, MD

Always discuss trial participation with your own doctor first.

Locations (33)

HonorHealth Research InsisuteScottsdale, Arizona, United StatesRecruiting
UC San Diego Moores Cancer CenterLa Jolla, California, United StatesRecruiting
The Angeles Clinic and Research InstituteLos Angeles, California, United StatesRecruiting
University of California Los AngelesLos Angeles, California, United StatesRecruiting
Stanford Cancer InstitutePalo Alto, California, United StatesRecruiting
University of Colorado Hospital - Anschutz Cancer Pavilion(ACP)Aurora, Colorado, United StatesRecruiting
The Melanoma & Skin Cancer InstituteEnglewood, Colorado, United StatesRecruiting
Georgetown University Medical CenterWashington D.C., District of Columbia, United StatesRecruiting
Mayo Clinic - Jacksonville FLJacksonville, Florida, United StatesRecruiting
Sylvester Comprehensive Cancer CenterMiami, Florida, United StatesRecruiting
Emory Winship Cancer InstituteAtlanta, Georgia, United StatesRecruiting
Northwestern Memorial HospitalChicago, Illinois, United StatesRecruiting

+ 21 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06581406