The purpose of this study is to evaluate the safety and efficacy of a novel RAS(ON)
inhibitor compared to docetaxel.
Additional locations may be listed on ClinicalTrials.gov for NCT06881784.
Locations matching your search criteria
United States
Maryland
Baltimore
Johns Hopkins University/Sidney Kimmel Cancer CenterStatus: Active
Name Not Available
Michigan
Detroit
Wayne State University/Karmanos Cancer InstituteStatus: Active
Name Not Available
Missouri
Saint Louis
Siteman Cancer Center at Washington UniversityStatus: Active
Name Not Available
New York
Bronx
Montefiore Medical Center-Weiler HospitalStatus: Active
Name Not Available
New York
Memorial Sloan Kettering Cancer CenterStatus: Active
Name Not Available
North Carolina
Chapel Hill
UNC Lineberger Comprehensive Cancer CenterStatus: Active
Name Not Available
Texas
Houston
M D Anderson Cancer CenterStatus: Active
Name Not Available
This is a global, randomized, open-label, Phase 3 study designed to evaluate whether
treatment with daraxonrasib will improve progression free survival (PFS) or overall
survival (OS) compared to docetaxel chemotherapy in patients with NSCLC who were
previously treated. Patients will be randomized in a 1:1 ratio to receive daraxonrasib or
docetaxel chemotherapy.
Lead OrganizationRevolution Medicines, Inc.