This is an open-label, randomized, multicenter Phase 2 study to assess the efficacy and
safety of FOLFIRI + bevacizumab + pelareorep vs. FOLFIRI + bevacizumab in patients with
RAS-mutated, MSS mCRC who have progressed after one prior line of oxaliplatin-based
therapy.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07446322.
Approximately 60 patients will be randomized 1:1 to the following study arms:
- Arm A: FOLFIRI + bevacizumab + pelareorep
- Arm B: FOLFIRI + bevacizumab The primary endpoint is ORR as assessed by the
investigator per RECIST 1.1. OS, PFS, and assessment of the safety and tolerability
of the study treatment combinations are secondary endpoints. The primary endpoint
analysis will be performed after all patients have had at least one tumor assessment
following initiation of study treatment or have progressed. The secondary endpoint
analyses will take place at EOS.
Lead OrganizationOncolytics Biotech