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A Study to Evaluate INCB161734 in Participants With Advanced or Metastatic Solid Tumors With KRAS G12D Mutation

NCT 06179160

Brief Summary

This study is conducted to determine the safety and tolerability of INCB161734 as a single agent or in combination with other anticancer therapies.

Intervention / Treatment 

  • Drug: INCB161734
  • Drug: Cetuximab
  • Drug: Retifanlimab
  • Drug: GEMNabP
  • Drug: mFOLFIRINOX
  • Drug: FOLFOX
  • Drug: FOLFIRI
  • Drug: INCA33890

Inclusion Criteria:

  • ≥18 years old.
  • Locally advanced or metastatic solid tumor with KRAS G12D mutation.
  • For Part 1a and Part 2 Combination Groups 1, 2, and 7: Disease progression on prior standard treatment, intolerance to or ineligibility for standard treatment, declined available therapies that are known to confer clinical benefit, or no standard available treatment to improve the disease outcome.
  • Cohort specific requirements aas defined in the protocol.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

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