IMA203
Sponsors
Immatics US Inc., Immatics US, Inc.
Conditions
Cutaneous MelanomaMelanoma, Cutaneous MalignantSolid tumorsSynovial Sarcomacutaneous malignantmelanoma
Phase 1
Phase 1/2 study evaluating genetically modified autologous T cells expressing a T-cell receptor recognizing a cancer/germline antigen as monotherapy or in combination with nivolumab in patients with recurrent and/or refractory solid tumors (ACTengine® IMA203-101)
RecruitingCTIS2024-515114-41-00
Start: 2020-08-10Target: 272Updated: 2025-12-29
ACTengine® IMA203 Combined With mRNA-4203
RecruitingNCT06946225
Start: 2025-07-25End: 2029-08-31Target: 15Updated: 2026-01-08
Phase 3
SUPRAME-ACTengine® IMA203 vs. Investigator's Choice of Treatment in Previously Treated, Unresectable or Metastatic Cutaneous Melanoma
RecruitingNCT06743126
Start: 2025-01-14End: 2031-10-01Target: 360Updated: 2026-03-19
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)
RecruitingCTIS2024-517062-42-00
Start: 2025-05-02Target: 84Updated: 2025-12-18