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FOLFIRI and Bevacizumab With or Without Pelareorep for Second-Line Treatment of Metastatic RAS-Mutated, Microsatellite-Stable Colorectal Cancer
Trial Status: active
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.
Inclusion Criteria
Histologically confirmed cancer of the colon or rectum with documented metastasis
Measurable disease per RECIST v. 1.1
Not candidates for curative surgery or curative radiation
Progressed on, or been intolerant to, a first-line, oxaliplatin-based chemotherapy regimen in the metastatic setting or relapsed within 6 months of completing adjuvant oxaliplatin
Considered medically eligible to receive standard of care (SOC) FOLFIRI with bevacizumab
Non-microsatellite instability high or non-deficient mismatch repair (non-MSI-H/non dMMR) tumor status per a standard local testing method
Tumor confirmed to harbor a known RAS mutation per a standard local testing method
ECOG performance status of 0 or 1
Patients must have adequate hematological, renal, and hepatic function
Female patients of childbearing potential must have a negative pregnancy test
Life expectancy of at least 6 months
Exclusion Criteria
Undergone systemic chemotherapy, radiotherapy, or surgery, <4 weeks before study treatment
Ongoing AEs of Grade ≥2 that are related to anti-cancer treatment
Prior treatment with irinotecan
Symptomatic brain metastases
Active autoimmune disease
Receiving immunosuppressive or myelosuppressive medications
Active, uncontrolled infections
Known HIV infection or active hepatitis B or C that requires anti-viral treatment
History of another primary cancer within the last 3 years except for non-melanoma skin cancer, early-stage prostate cancer, or curatively treated cervical carcinoma in-situ
History of allergy or known hypersensitivity to any of the study drugs, study drug classes,
Uncontrolled or severe cardiac disease
Received any vaccine within 28 days prior to first study treatment
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07446322.
Locations matching your search criteria
United States
Georgia
Atlanta
Emory University Hospital/Winship Cancer Institute
Status: Approved
Name Not Available
Michigan
Detroit
Wayne State University/Karmanos Cancer Institute
Status: Approved
Name Not Available
Texas
Houston
UT MD Anderson Cancer Center
Status: Approved
Name Not Available
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