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Study of RMC-6236 in Patients With Advanced Solid Tumors Harboring Specific Mutations in RAS

Eligible age

18+ yrs

Accepts

All genders

Locations

13 states

Healthy volunteers

No

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About this study

Evaluate the safety and tolerability of RMC-6236 in adults with specific RAS mutant advanced solid tumors.

Sponsor: Revolution Medicines, Inc.

You may qualify if…

  • ✓ Histologically confirmed advanced solid tumor with specific KRAS G12 mutations (dose escalation) or RAS mutations (dose optimization/expansion) identified through deoxyribonucleic acid (DNA) sequencing. PDAC with wild-type RAS (expansion).
  • ✓ Treatment naive or have received prior standard therapy appropriate for tumor type and stage
  • ✓ Have Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • ✓ Adequate organ function

You may not qualify if…

  • ✕ Primary central nervous system (CNS) tumors
  • ✕ Active, untreated brain metastases
  • ✕ Known or suspected impairment of gastrointestinal function that may prohibit ability to swallow or absorb an oral medication
  • ✕ History of any other unstable or clinically significant concurrent medical condition that would, in the opinion of the investigator, jeopardize the safety of a participant, impact their expected survival through the end of the study participation, and/or impact their ability to comply with the protocol prior/concomitant therapy
  • ✕ Other inclusion/exclusion criteria may apply.

Where it's recruiting

California

Orange · Santa Monica

Florida

Tampa

Georgia

Atlanta

Louisiana

Baton Rouge

Maryland

Baltimore

New York

New York

Ohio

Cincinnati · Maumee

Tennessee

Chattanooga · Nashville

Texas

Austin · Dallas · Houston · San Antonio

Utah

Salt Lake City

Virginia

Fairfax

Source: ClinicalTrials.gov · NCT05379985 · last updated 2026-05-15

Study of RMC-6236 in Patients With Advanced Solid Tumors Harboring Spe · TrialPath