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Study of Elironrasib and Daraxonrasib as Monotherapies and Combination Therapy in Participants With Advanced KRAS G12C Mutant Solid Tumors
NCT06128551 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- DRUG Elironrasib
- DRUG Daraxonrasib
Study Locations (20)
Texas
- Mary Crowley Cancer Research — Dallas
- MD Anderson — Houston
- NEXT Dallas — Irving
- NEXT Oncology San Antonio — San Antonio
- START Texas — San Antonio
California
- City of Hope — Duarte
- UC IRVINE Health — Orange
- UC Davis Comprehensive Cancer Center — Sacramento
- Stanford Cancer Institute — Stanford
New York
- Columbia University — New York
- NYU Langone Health — New York
- Memorial Sloan Kettering Cancer Center — New York
Florida
- Florida Cancer Specialists — Sarasota
- Moffitt Cancer Center and Research Institute — Tampa
Michigan
- Henry Ford Cancer — Detroit
- START Midwest — Grand Rapids
Colorado
- University of Colorado Cancer Center — Aurora
Massachusetts
- Dana Farber Cancer Institute — Boston
Oklahoma
- University of Oklahoma — Oklahoma City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 534 participants |
| Start Date | 2023-11-14 |
| Est. Completion | 2029-06 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06128551
The ClinicalTrials.gov registry entry for NCT06128551 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 534 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Revolution Medicines, which has 66 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Colorectal Cancer appearing as the primary indexed condition, and to 2 interventions — of which Elironrasib is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06128551 reports 20 study locations spanning 9 distinct geographic areas — top geographies include Texas, California, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06128551 about?
NCT06128551 is a clinical study titled "Study of Elironrasib and Daraxonrasib as Monotherapies and Combination Therapy in Participants With Advanced KRAS G12C Mutant 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.
What is the current status of trial NCT06128551?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 534 participants. The study started on 2023-11-14. Estimated completion is 2029-06.
What conditions does trial NCT06128551 study?
This clinical trial studies the following conditions: Colorectal Cancer, Pancreatic Ductal Adenocarcinoma, Non-Small Cell Lung Cancer (NSCLC). These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06128551?
The interventions under investigation include: Elironrasib (DRUG), Daraxonrasib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06128551?
This trial is sponsored by Revolution Medicines, which has 66 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06128551 being conducted?
This trial has 20 study locations across California, Colorado, Florida, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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