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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take RMC-5127
  • 2.Take cetuximab
  • 3.Take daraxonrasib
PhasePhase 1
Drugcetuximab
Routeinjection
Primary goalDose Limiting Toxicities

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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