CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 110 enrolled
Drug / intervention
Nivolumab +5 moredrug
Likely dose
RO7247669 2100 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05116202
NCT05116202Phase 2Completed

A Phase Ib/II, Open-Label, Multicenter, Randomized Umbrella Study Evaluating the Efficacy and Safety of Multiple Treatment Combinations in Patients With Melanoma (Morpheus-Melanoma)

Hoffmann-La Roche·interventional·Posted Nov 10, 2021·Updated Jul 18, 2025

In Brief

A Phase 2 clinical trial evaluating Nivolumab, Ipilimumab, and 4 other interventions for Melanoma. Completed, enrolled 110 participants across 14 sites in 5 countries.

Detailed Summary

This study will evaluate the efficacy, safety, and pharmacokinetics of treatment combinations in cancer immunotherapy (CIT)-naive participants with resectable Stage III melanoma (Cohort 1) and in participants with Stage IV melanoma (Cohort 2). The study is designed with the flexibility to open new treatment arms as new treatments become available, close existing treatment arms that demonstrate minimal clinical activity or unacceptable toxicity, and modify the participant population.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMelanoma
CountriesAustralia, France, Italy, Spain, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20222023202420252026
First PostedNov 10, 2021
Enrollment StartFeb 2, 2022
Primary CompletionSep 22, 2023
Study CompletionMay 28, 2024
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 4.6 years ago

Interventions

Nivolumabdrug

Nivolumab will be administered at a dose of 3 mg/kg IV on Day 1 of each 21 day cycle.

Ipilimumabdrug

Ipilimumab will be administered at a dose of 1 mg/kg by IV on Day 1 of each 21 day cycle.

RO7247669 2100 mgdrug

RO7247669 will be administered at a dose of 2100 mg by IV infusion on Day 1 of each 21 day cycle.

Atezolizumabdrug

Atezolizumab will be administered at a dose of 1200 mg IV on Day 1 of each 21 day cycle.

Tiragolumabdrug

Tiragolumab will be administered at a dose of 600 mg IV on Day 1 of each 21 day cycle.

RO7247669 600 mgdrug

RO7247669 will be administered at a dose of 600 mg by IV infusion on Day 1 of each 21 day cycle.