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Study of RMC-6236 in Patients With Advanced Solid Tumors Harboring Specific Mutations in RAS

RecruitingPhase 1/2

A Multicenter Open-Label Study of RMC-6236 in Patients With Advanced Solid Tumors Harboring Specific Mutations in RAS

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Histologically confirmed advanced solid tumor with specific KRAS G12 mutations (dose escalation) or RAS mutations (dose optimization/expansion) identified through deoxyribonucleic acid (DNA) sequencing. PDAC with wild-type RAS (expansion).
* Treatment naive or have received prior standard therapy appropriate for tumor type and stage
* Have Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
* Adequate organ function

Exclusion Criteria:

* Primary central nervous system (CNS) tumors
* Active, untreated brain metastases
* Known or suspected impairment of gastrointestinal function that may prohibit ability to swallow or absorb an oral medication
* History of any other unstable or clinically significant concurrent medical condition that would, in the opinion of the investigator, jeopardize the safety of a participant, impact their expected survival through the end of the study participation, and/or impact their ability to comply with the protocol prior/concomitant therapy

Other inclusion/exclusion criteria may apply.

About the study

Evaluate the safety and tolerability of RMC-6236 in adults with specific RAS mutant advanced solid tumors.

What is being tested

Sponsor: Revolution Medicines, Inc. · Participants: 754 · Started: May 31, 2022

Contact the study team

Official record on ClinicalTrials.gov — NCT05379985

Locations in the U.S.

CaliforniaUC Irvine/Chao Family Comprehensive Cancer Center, Orange
UCLA, Santa Monica
FloridaMoffitt Cancer Center, Tampa
GeorgiaPiedmont Healthcare, Atlanta
LouisianaMary Bird Perkins Cancer Center, Baton Rouge
MarylandJohns Hopkins University, Baltimore
MassachusettsDana Farber Cancer Institute, Boston
New YorkColumbia University, New York
Memorial Sloan-Kettering Cancer Center, New York
Perlmutter Cancer Center at NYU Langone Health, New York
OhioChrist Hospital Cancer Center, Cincinnati
Taylor Cancer Research Center, Maumee
TennesseeTennessee Oncology, Chattanooga
Sarah Cannon Research Institute, Nashville
TexasUniversity of Texas at Austin, Austin
Mary Crowley Cancer Research, Dallas
The University of Texas MD Anderson Cancer Center, Houston
Next Oncology, San Antonio
UtahHuntsman Cancer Institute, Salt Lake City
VirginiaNext Oncology Virginia, Fairfax
WashingtonVirginia Mason Medical Center, Seattle

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.