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Study details
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Study of RMC-5127 in Patients With Advanced KRAS G12V-Mutant Solid Tumors

Revolution Medicines, Inc.
NCT IDNCT07349537ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

574

Study length

about 2.8 years

Ages

18+

Locations

5 sites in MI, TX, VA

What this study is about

This trial is testing a treatment called RMC-5127 for people with advanced solid tumors that have the KRAS G12V mutation. The trial will evaluate how safe and effective this treatment is, as well as its effects on the body's ability to process the drug.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take RMC-5127
  • 2.Take cetuximab
  • 3.Take daraxonrasib

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

cetuximab

Drug routes

injection (Injection)

Endpoints

Primary: Dose Limiting Toxicities, Number of patients with adverse events (AEs)

Secondary: AUC concentrations of RMC-5127 and daraxonrasib, Cmax concentrations of RMC-5127 and daraxonrasib, Duration of Response (DOR), Half-Life of RMC-5127 and daraxonrasib, Objective Response Rate (ORR), Tmax concentration of RMC-5127 and daraxonrasib

Body systems

Oncology