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Active, not recruiting Phase 1 Interventional

Dose Escalation and Dose Expansion Study of RMC-6291 Monotherapy in Subjects With Advanced KRASG12C Mutant Solid Tumors

ClinicalTrials.gov ID: NCT05462717

Public ClinicalTrials.gov record NCT05462717. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 12:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 1/1b, Multicenter, Open-Label, Dose Escalation and Dose Expansion Study of RMC-6291 Monotherapy in Subjects With Advanced KRASG12C Mutant Solid Tumors

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of escalating doses of RMC-6291 (KRAS G12C(ON) inhibitor) monotherapy in adult subjects with advanced solid tumors and to identify the maximum tolerated dose (MTD), and the recommended Phase 2 dose.

Study identification

NCT ID
NCT05462717
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
Revolution Medicines, Inc.
Industry
Enrollment
222 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 19, 2022 (Actual)
Primary completion
Mar 31, 2027 (Estimated)
Completion
Sep 30, 2027 (Estimated)
Last update posted
May 15, 2026

2022 – 2027

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
Highlands Oncology Group Springdale Arkansas 72762 —
UC Irvine Cancer Center Orange California 92868 —
UC Davis Cancer Center Sacramento California 95817 —
UCSF San Francisco California 94158 —
University of Miami School of Medicine Sylvester Comprehensive Cancer Center Miami Florida 33136 —
Moffitt Cancer Center Tampa Florida 33612 —
American Oncology Partners of Maryland Bethesda Maryland 20817 —
Dana-Farber Cancer Institute Boston Massachusetts 02215 —
Roswell Park Comprehensive Cancer Center Buffalo New York 14203 —
MSK Cancer Center New York New York 10021 —
Columbia University Irving Medical Center New York New York 10032 —
Tennessee Oncology Nashville Tennessee 37203 —
Next Oncology San Antonio Texas 78229 —
START San Antonio Texas 78229 —
Next Oncology Virginia Fairfax Virginia 22031 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 49 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05462717, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 15, 2026 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05462717 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →