FOLFIRI and Bevacizumab With or Without Pelareorep for Second-Line Treatment of Metastatic RAS-Mutated, Microsatellite-Stable Colorectal Cancer
Recruiting · NCT07446322 · Interventional (participants receive a specific treatment) · Lead sponsor: Oncolytics Biotech
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
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.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 2
Study type
Interventional (participants receive a specific treatment)
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
Where it is running
13 locations listed across 7 US states.
- Central Alabama Research - Homewood, Alabama, United States
- Clinical Research Advisors (Beverly Hills) - Beverly Hills, California, United States
- Clinical Research Advisors (Encino) - Encino, California, United States
- Clinical Research Advisors (Korea Town) - Koreatown, California, United States
- Clinical Research Advisors (Downtown LA) - Los Angeles, California, United States
- Clinical Research Advisors (West Hollywood) - Los Angeles, California, United States
- Clinical Research Advisors (West Covina) - West Covina, California, United States
- Emory Winship Cancer Institute - Atlanta, Georgia, United States
- Community Health Network - Indianapolis, Indiana, United States
- Washington University School of Medicine - St Louis, Missouri, United States
- Summit Health Cancer Center - Florham Park, New Jersey, United States
- Rutgers Cancer Institute - New Brunswick, New Jersey, United States
- Gabrail Cancer Center - Canton, Ohio, United States