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Taking people in NetherlandsPhase 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
Amsterdam, NetherlandsSee the site
Phase
Phase 1/2

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with advanced or metastatic solid tumors that carry a KRAS G12C mutation and were treated before. Lung, colorectal and pancreatic cancers are included.

Age
18 years or older
Sex
All sexes can join.
Disease stage
Advanced or metastatic solid tumor with a KRAS G12C mutation, not open to treatment meant to remove all of the disease. ECOG performance status 0 or 1.
Earlier treatment
Solid tumors must have been treated before. For one part of the study, lung cancer must have been treated with immunotherapy, chemotherapy and KRAS G12C (OFF) inhibitors. Other solid tumors must not have had KRAS G12C (OFF) inhibitors.
Biomarker or test result
KRAS G12C mutation, documented by pathology.

Main reasons for not taking part

  • Primary central nervous system (CNS) tumors
  • Active brain metastases
  • Known problem of the gut that would change how drugs are absorbed
  • Major surgery within 28 days before treatment
  • Minor procedures not related to the study within 7 days before treatment

Read by machine on 9 November 2026.

Where in Netherlands

  • Netherlands Cancer Institute-Antoni van LeeuwenhoekAmsterdam, NetherlandsTaking 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?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

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