IMC-F106C Regimen Versus Nivolumab Regimens in Previously Untreated Advanced Melanoma (PRISM-MEL-301)

This is a phase 3, randomized, controlled study of brenetafusp (IMC-F106C) plus nivolumab compared to standard nivolumab regimens in HLA-A\*02:01-positive participants with previously untreated advanced melanoma.

Trial Details

NCT ID
NCT06112314
Phase
PHASE3
Sponsor
Immunocore Ltd
Status
RECRUITING
Cancer Type
Melanoma
Interventions
  • Brenetafusp
  • Nivolumab
  • Nivolumab + Relatlimab
Locations (sample)
  • Tucson, Arizona, United States|32.22174,-110.92648
  • La Jolla, California, United States|32.84727,-117.2742
  • Los Angeles, California, United States|34.05223,-118.24368
  • Los Angeles, California, United States|34.05223,-118.24368
  • Los Angeles, California, United States|34.05223,-118.24368

Key Eligibility Criteria

  • Participants must be HLA-A\*02:01-positive
  • Participants must have histologically confirmed Stage IV or unresectable Stage III melanoma
  • Archived or fresh tumor tissue sample that must be confirmed as adequate
  • Participants must have measurable disease per RECIST 1.1

For full eligibility, visit ClinicalTrials.gov.

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