A Phase 2 study evaluating STRO-002 in subjects with previously treated advanced or
metastatic non-small cell lung cancer expressing FOLR1
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06555263.
This is a multicenter, open-label study. The study is designed to assess the preliminary
efficacy and safety of luveltamab tazevibulin, an anti-FOLR1 antibody drug conjugate
(ADC) in previously treated subjects with advanced or metastatic NSCLC that expresses
FOLR1.
Subjects will receive luveltamab tazevibulin administered intravenously every 3 weeks
until disease progression, intolerable toxicity, elective withdrawal from the study, or
study termination.
Lead OrganizationSutro Biopharma, Inc.