A Phase 2 Study of VS-7375 in Patients With KRAS G12D-Mutated Colorectal Cancer

This study will assess the safety and efficacy of VS-7375 alone and in combination with cetuximab or panitumumab and cetuximab plus mFOLFOX in patients with metastatic KRAS G12D - mutated Colorectal Cancer

Trial Details

NCT ID
NCT07659795
Phase
PHASE2
Sponsor
Verastem, Inc.
Status
RECRUITING
Cancer Type
Colorectal Cancer
Interventions
  • VS-7375
  • cetuximab
  • panitumumab
  • Cetuximab + mFOLFOX6
Locations (sample)
  • Los Angeles, California, United States|34.05223,-118.24368
  • Los Angeles, California, United States|34.05223,-118.24368
  • Tampa, Florida, United States|27.94752,-82.45843
  • Grand Rapids, Michigan, United States|42.96336,-85.66809
  • East Brunswick, New Jersey, United States|40.42788,-74.41598

Key Eligibility Criteria

  • Histopathology confirmed metastatic CRC
  • Measurable disease per RECIST 1.1
  • Local testing confirmed KRAS G12D mutation (tissue required for confirmatory central testing)
  • ECOG PS=0 or 1

For full eligibility, visit ClinicalTrials.gov.

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