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Taking people in Puerto RicoPhase 1/2

Tests elironrasib and daraxonrasib in advanced solid tumors with KRAS G12C mutation

Tests two drugs, alone and together, in adults with advanced KRAS G12C-mutated cancers.

Plain-language title generated from the registry record
Registry title: Study of Elironrasib and Daraxonrasib as Monotherapies and Combination Therapy in Participants With Advanced KRAS G12C Mutant Solid Tumors

Key facts

Where
San Juan, Puerto RicoSee the site
Phase
Phase 1/2

Where in Puerto Rico

  • Pan American Center for Oncology TrialsSan Juan, Puerto RicoTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Revolution Medicines, Inc.
Trial code
NCT06128551
Record updated
22 September 2026
Original description
This study is to evaluate the safety, tolerability, and PK profiles of Elironrasib and Daraxonrasib as monotherapies and combination therapy in patients with KRAS G12C-mutated solid tumors.Read full original descriptionShow less

Phase 1b/2, Multicenter, Open-label, Dose Escalation and Dose Expansion Study of Elironrasib and Daraxonrasib as Monotherapies and Combination Therapy in Patients With Advanced KRAS G12C-Mutated Solid Tumors

This study is to evaluate the safety, tolerability, and PK profiles of Elironrasib and Daraxonrasib as monotherapies and combination therapy in patients with KRAS G12C-mutated solid tumors.

Inclusion: 18 years of age; Histology: pathologically documented, KRAS G12C-mutated, advanced or metastatic solid tumors not amendable to curative therapy; Phase 1b Dose Escalation: solid tumors, previously treated; Phase 1b Dose Expansion and Phase 2:; NSCLC, previously treated with immunotherapy, chemotherapy, and KRAS G12C (OFF) inhibitors ii. Solid tumors, previously treated, naïve to KRAS G12C (OFF) inhibitors; ECOG performance status 0 or 1; Adequate organ function.

Exclusion: Major surgical procedures within 28 days or non-study related minor procedures within 7 days of treatment; Known impairment of GI function that would alter the absorption; Primary central nervous system (CNS) tumors; Active brain metastases.

ClinicalTrials.gov NCT06128551