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 sponsor and potential other locations can be found on ClinicalTrials.gov for NCT05462717.
Locations matching your search criteria
United States
Florida
Tampa
Moffitt Cancer CenterStatus: Active
Name Not Available
This is an open-label, multicenter, Phase 1/1b study of RMC-6291 monotherapy in subjects
with advanced KRASG12C-mutant solid tumors. The study will include 2 components: a
Dose-Escalation and a Dose-Expansion. Subjects will be treated until disease progression
per RECIST v1.1, unacceptable toxicity, or other criteria for withdrawal are met,
whichever occurs first.
Lead OrganizationRevolution Medicines