drugset / Trial / NCT06581406

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

NCT06581406

Phase 2/3 Recruiting 280 enrolled Replimune, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

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.

Timeline

Start
2024-12-17
Primary completion
2030-01
Completion
2031-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipilimumab Monoclonal antibody
Subject RP2 Other / unclassified
Background Nivolumab Monoclonal antibody

Indications