🏛️ Verified NIH Record • Updated 2026-08-20

Study of Sotorasib, Panitumumab and FOLFIRI Versus FOLFIRI With or Without Bevacizumab-awwb in Treatment-naïve Participants With Metastatic Colorectal Cancer With KRAS p.G12C Mutation (NCT06252649)

Phase 3 Multicenter, Randomized, Open-label, Active-controlled Study of Sotorasib, Panitumumab and FOLFIRI Versus FOLFIRI With or Without Bevacizumab-awwb for Treatment-naïve Subjects With Metastatic Colorectal Cancer With KRAS p.G12C Mutation (CodeBreaK 301)

🟢 Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: Amgen

🩺 Plain-English Summary (8th-Grade Level)

The aim of this study is to compare progression free survival (PFS) in treatment-naïve participants with KRAS p.G12C mutated metastatic colorectal cancer (mCRC) receiving sotorasib, panitumumab and FOLFIRI vs FOLFIRI with or without bevacizumab-awwb.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (5 items) and avoid the listed exclusions (5 items).

Location: Ironwood Cancer and Research Centers Scottsdale — Chandler, Arizona

Age range: 18 Years

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Usually NOT eligible if any of the following apply:

  • Exclusion Criteria:
  • Active, untreated brain metastases.
  • Leptomeningeal disease
  • Previous treatment with a KRAS p.G12C inhibitor
  • History of interstitial pneumonitis or pulmonary fibrosis or evidence of interstitial pneumonitis or pulmonary fibrosis on baseline CT scan

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (291 Sites)

Showing the first 25 of 291 sites.

  • Ironwood Cancer and Research Centers Scottsdale — Chandler, Arizona
  • Providence Saint Jude Medical Center — Fullerton, California
  • City of Hope National Medical Center — Long Beach, California
  • Cancer and Blood Research Center, LLC — Los Alamitos, California
  • California Research Institute — Los Angeles, California
  • Norwalk Hospital — Norwalk, Connecticut
  • Cancer Specialists of North Florida - Southpoint — Jacksonville, Florida
  • D and H Cancer Research Center — Margate, Florida
  • Mid Florida Hematology and Oncology Centers PA — Orange City, Florida
  • Boca Raton Clinical Research Medical Center Inc — Plantation, Florida
  • Georgia Cancer Specialists — Atlanta, Georgia
  • Insight Research Institute — Chicago, Illinois
  • Hope and Healing Cancer Services — Hinsdale, Illinois
  • Orchard Healthcare Research Inc — Skokie, Illinois
  • Pikeville Medical Center — Pikeville, Kentucky
  • Henry Ford Health System — Detroit, Michigan
  • Cancer and Hematology Centers of Western Michigan — Grand Rapids, Michigan
  • Saint Louis Cancer Care West County — Bridgeton, Missouri
  • Minniti Center for Medical Oncology and Hematology — Mickleton, New Jersey
  • Duke Cancer Center — Durham, North Carolina
  • FirstHealth Cancer Center — Pinehurst, North Carolina
  • Thomas Jefferson University — Philadelphia, Pennsylvania
  • Carolina Blood and Cancer Care — Rock Hill, South Carolina
  • Tennessee Oncology PLLC - Chattanooga — Nashville, Tennessee
  • Tennessee Oncology, PLLC — Nashville, Tennessee

📞 Contact the Study Coordinator

Phone: (866) 572-6436

Email: medinfo@amgen.com

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

💰 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 § 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.

💡 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.
🏛️ View Official NIH Record ↗