๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-06-15

Study of Onvansertib in Combination With FOLFIRI and Bevacizumab or FOLFOX and Bevacizumab Versus FOLFIRI and Bevacizumab or FOLFOX and Bevacizumab for First-Line Treatment of Metastatic Colorectal Cancer in Adult Participants With a KRAS or NRAS Mutation (NCT06106308)

A Phase 2, Randomized, Open-label Study of Onvansertib in Combination With FOLFIRI and Bevacizumab or FOLFOX and Bevacizumab Versus FOLFIRI and Bevacizumab or FOLFOX and Bevacizumab for First-line Treatment of Metastatic Colorectal Cancer in Patients With a KRAS or NRAS Mutation

๐Ÿ”ต Active, Not Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Cardiff Oncology

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The purpose of this study is to assess 2 different doses of onvansertib to select the lowest dose that is maximally effective, and to assess the safety, efficacy, pharmacokinetics, and pharmacodynamics of onvansertib in combination with FOLFIRI + bevacizumab or FOLFOX + bevacizumab in patients with KRAS or NRAS-mutated metastatic colorectal cancer (CRC) in the first-line setting.

Who can join: Review the eligibility criteria below.

Location: Mayo Clinic - Arizona โ€” Phoenix, Arizona

Age range: 18 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (41 Sites)

Showing the first 25 of 41 sites.

  • Mayo Clinic - Arizona โ€” Phoenix, Arizona
  • The University of Arizona Cancer Center โ€” Tucson, Arizona
  • St. Bernards Medical Center โ€” Jonesboro, Arkansas
  • Highlands Oncology Group โ€” Springdale, Arkansas
  • Pacific Cancer Medical Center โ€” Anaheim, California
  • Comprehensive Blood and Cancer Center - Bakersfield โ€” Bakersfield, California
  • Orange Coast Memorial Medical Center โ€” Fountain Valley, California
  • UC San Diego Moores Cancer Center โ€” La Jolla, California
  • Norris Comprehensive Cancer Center โ€” Los Angeles, California
  • UCLA Department of Medicine-Hematology/Oncology โ€” Los Angeles, California
  • Sharp Memorial Hospital โ€” San Diego, California
  • Torrance Memorial Physician Network - Cancer Care and Infusion Center โ€” Torrance, California
  • PIH Health โ€” Whittier, California
  • Memorial Cancer Institute โ€” Hollywood, Florida
  • Mayo Clinic - Florida โ€” Jacksonville, Florida
  • Cleveland Clinic Martin Health โ€” Stuart, Florida
  • Kaiser Permanente โ€” Honolulu, Hawaii
  • Fort Wayne Medical Oncology and Hematology โ€” Fort Wayne, Indiana
  • The University of Kansas Cancer Center - Westwood โ€” Westwood, Kansas
  • Cancer Center of Kansas โ€” Wichita, Kansas
  • Cancer & Hematology Centers of Western Michigan - Lemmen-Holton Cancer Pavilion โ€” Grand Rapids, Michigan
  • Mayo Clinic Cancer Center โ€” Rochester, Minnesota
  • Saint Luke's Hospital โ€” Kansas City, Missouri
  • Washington University School of Medicine Center for Advanced Medicine โ€” St Louis, Missouri
  • CCCN โ€” Las Vegas, Nevada

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 664-4580

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—