๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-05-19

Studying Chemotherapy With or Without Panitumumab for Unresectable, Locally Advanced, or Metastatic Pancreatic Cancer Without KRAS Mutations (NCT06998940)

Randomized Phase III Study of Second-Line Chemotherapy With or Without Panitumumab for KRAS Wild Type, Locally Advanced or Metastatic Pancreatic Adenocarcinoma

๐ŸŸข Recruiting Phase3 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: SWOG Cancer Research Network

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

This phase III trial compares the effect of adding panitumumab to standard chemotherapy (with nanoliposomal Irinotecan, leucovorin, and 5-fluorouracil \[5-FU\] or irinotecan, leucovorin, and 5-FU or nab-paclitaxel and gemcitabine) versus standard chemotherapy alone in treating patients with KRAS wild type (WT) pancreatic ductal adenocarcinoma that cannot be removed by sugery (unresectable) or that has spread to nearby tissue or lymph nodes (locally advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic). Panitumumab is a monoclonal antibody that may interfere with the ability of tumor cells to grow and spread. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Chemotherapy drugs, such as nanoliposomal irinotecan, leucovorin, 5-FU, irinotecan, nab-paclitaxel and gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Adding panitumumab to standard chemotherapy may be effective in treating patients with unresectable, locally advanced, or metastatic KRAS WT pancreatic ductal adenocarcinoma.

Who can join: Review the eligibility criteria below.

Location: Anchorage Associates in Radiation Medicine โ€” Anchorage, Alaska

Age range: 18 Years

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 (274 Sites)

Showing the first 25 of 274 sites.

  • Anchorage Associates in Radiation Medicine โ€” Anchorage, Alaska
  • Alaska Breast Care and Surgery LLC โ€” Anchorage, Alaska
  • Alaska Oncology and Hematology LLC โ€” Anchorage, Alaska
  • Alaska Women's Cancer Care โ€” Anchorage, Alaska
  • Katmai Oncology Group โ€” Anchorage, Alaska
  • Providence Alaska Medical Center โ€” Anchorage, Alaska
  • Cancer Center at Saint Joseph's โ€” Phoenix, Arizona
  • Highlands Oncology Group - Fayetteville โ€” Fayetteville, Arkansas
  • NEA Baptist Memorial Hospital and Fowler Family Cancer Center - Jonesboro โ€” Jonesboro, Arkansas
  • Highlands Oncology Group - Rogers โ€” Rogers, Arkansas
  • Highlands Oncology Group โ€” Springdale, Arkansas
  • Mission Hope Medical Oncology - Arroyo Grande โ€” Arroyo Grande, California
  • Sutter Auburn Faith Hospital โ€” Auburn, California
  • Sutter Cancer Centers Radiation Oncology Services-Auburn โ€” Auburn, California
  • Alta Bates Summit Medical Center-Herrick Campus โ€” Berkeley, California
  • Providence Saint Joseph Medical Center/Disney Family Cancer Center โ€” Burbank, California
  • Mills-Peninsula Medical Center โ€” Burlingame, California
  • Sutter Cancer Centers Radiation Oncology Services-Cameron Park โ€” Cameron Park, California
  • Mercy Cancer Center - Carmichael โ€” Carmichael, California
  • Mercy San Juan Medical Center โ€” Carmichael, California
  • Eden Hospital Medical Center โ€” Castro Valley, California
  • Sutter Davis Hospital โ€” Davis, California
  • Mercy Cancer Center - Elk Grove โ€” Elk Grove, California
  • Palo Alto Medical Foundation-Fremont โ€” Fremont, California
  • Mercy Cancer Center โ€” Merced, California

๐Ÿ“ž Contact the Study Coordinator

Phone: (907) 212-6871

Email: AKPAMC.OncologyResearchSupport@providence.org

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†—