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Clinical trial · no report yet · Phase 3

SUPRAME

SUPRAME-ACTengine® IMA203 vs. Investigator's Choice of Treatment in Previously Treated, Unresectable or Metastatic Cutaneous Melanoma

We haven't built a report for this trial yet. This page shows the registry record and the public commentary we found that names the trial. A report reads that commentary and sets out what clinicians said about the trial, each point linked to its source. How reports are made.

Preliminary discovery

Commentary in our index that names this trial so far

Podcasts, YouTube videos and X posts we have indexed. A report screens them, searches for more and cites what clinicians said when it is built, so final coverage is set at build.

ChannelFound
X threads5
Podcasts3
YouTube2
Bluesky threads1

The trial

ClinicalTrials.gov
Official title
A Prospective, Multicenter, Open-label, Randomized, Actively Controlled, Parallel-group Phase 3 Clinical Trial to Evaluate Efficacy, Safety, and Tolerability of IMA203 Versus Investigator's Choice of Treatment in Patients With Previously Treated, Unresectable or Metastatic Cutaneous Melanoma (ACTengine® IMA203-301)
Phase
Phase 3
Status
Recruiting
Conditions
Melanoma, Cutaneous Malignant
Interventions
IMA203; nivolumab plus relatlimab; lifileucel; nivolumab; pembrolizumab; ipilimumab; Dacarbazine; temozolomide; paclitaxel; paclitaxel plus carboplatin; Albumin-Bound Paclitaxel
Arms
  • Experimental arm · Experimental
  • Control arm- investigator's choice · Active comparator
Enrollment
360 (estimated)
Primary outcomes
  • Progression-free survival assessed by BICR
Sponsor
Immatics US, Inc.
Start
Jan 14, 2025
Primary completion
Jan 2028 (estimated)
Results posted
No
Registry record
NCT06743126 · updated Aug 18, 2026