A Study to Evaluate the Effectiveness and Safety of Setidegrasib, Given With Either mFOLFIRINOX or NALIRIFOX Chemotherapies, in People With Pancreatic Cancer (NCT07409272)
A Phase 3, Double-blind, Placebo-controlled, Randomized Study to Assess the Efficacy and Safety of ASP3082 in Combination With mFOLFIRINOX or NALIRIFOX as First-line Treatment in Participants With KRAS G12D Mutated Metastatic Pancreatic Adenocarcinoma
๐ฉบ Plain-English Summary (8th-Grade Level)
Pancreatic cancer is difficult to diagnose early. By the time people have been diagnosed, the cancer has usually spread to other parts of the body (metastatic). The standard treatment is chemotherapy, but other treatments are needed to improve outcomes in people with pancreatic cancer. The first treatment that people usually receive is chemotherapy. At the time this study started, some of the main standard chemotherapies for pancreatic cancer were mFOLFIRINOX or NALIRIFOX. Genes give your body instructions on how to make proteins. Proteins are needed to keep the body working properly. Many types of cancer are caused by changes in certain genes, making them faulty. Many people with pancreatic cancer have a faulty KRAS gene. One such change in the KRAS gene is called a G12D mutation. Researchers are looking for ways to stop the actions of abnormal proteins made from the KRAS G12D mutation. This study is about setidegrasib given with chemotherapy in people with pancreatic cancer who have the KRAS G12D mutation. Before setidegrasib can become an approved treatment, clinical studies need to be completed to understand how it works and how safe it is. The main aim is to learn if people who are given setidegrasib with chemotherapy live for longer than people who are given placebo with chemotherapy. Other aims are to learn if setidegrasib delays the cancer and symptoms returning, how the body processes setidegrasib, and its safety, when given with chemotherapy. People in this study will be adults with metastatic pancreatic cancer with the G12D mutation in their KRAS gene. Surgery or radiotherapy will not be an option to cure their cancer. People cannot take part if the cancer cells have spread to the thin tissue covering the brain and spinal cord (leptomeningeal disease), have symptoms of cancer in the brain or nervous system, or have recently had some other cancers that required treatment. In this study, people are given either setidegrasib with mFOLFIRINOX or NALIRIFOX chemotherapy, or a placebo with mFOLFIRINOX or NALIRIFOX chemotherapy. Whether people receive setidegrasib or placebo is decided by chance. The study doctor decides which chemotherapy (mFOLFIRINOX or NALIRIFOX) people receive. People will only receive NALIRIFOX chemotherapy (with setidegrasib or placebo) after the safety of setidegrasib with NALIRIFOX chemotherapy has been confirmed in another ongoing setidegrasib study. All of the study treatments are given slowly through a tube into a vein (infusion). People will continue to receive study treatment until their cancer gets worse, they can't tolerate the study treatment, they start other cancer treatment, they or the doctor decides the person should stop receiving study treatment, or sadly they pass away. There will be safety checks at each visit, and the doctors will continue to check for medical problems and people's wellbeing throughout the study.
Who can join: Review the eligibility criteria below.
Location: University of Arizona Cancer Center - North Campus โ Tucson, Arizona
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (62 Sites)
Showing the first 25 of 62 sites.
- University of Arizona Cancer Center - North Campus โ Tucson, Arizona
- Mercy Cancer Center โ Fort Smith, Arkansas
- Crosson Cancer Institute at Providence St. Jude Medical Center in Fullerton โ Fullerton, California
- UCI Health - Irvine โ Irvine, California
- Cedars-Sinai - Cedars-Sinai Medical Center โ Los Angeles, California
- Hoag Mem Hosp Presbyterian โ Newport Beach, California
- UC Irvine Health-Chao Family Comprehensive Cancer Center โ Orange, California
- Hartford Healthcare โ Hartford, Connecticut
- Baptist MD Anderson Cancer Institute โ Jacksonville, Florida
- Baptist Health Medical Group Oncology โ Miami, Florida
- Mount Sinai Medical Center - Miami Beach โ Miami Beach, Florida
- Piedmont Healthcare - Piedmont Physicians Medical Oncology Atlanta โ Atlanta, Georgia
- Indiana University Health - Indiana University Melvin and Bren Simon Comprehensive Cancer Center โ Indianapolis, Indiana
- Saint Elizabeth Medical Center, Inc. DBA St. Elizabeth Health Care โ Edgewood, Kentucky
- University of Maryland School - Division of Hematology/Oncology โ Baltimore, Maryland
- University of Michigan Health - University of Michigan Medical Center โ Ann Arbor, Michigan
- Allina Health Cancer Institute - Hematology Cancer Care Services โ Minneapolis, Minnesota
- HealthPartners Frauenshuh Cancer Center โ Saint Louis Park, Minnesota
- HealthPartners Cancer Center at Regions Hospital โ Saint Paul, Minnesota
- Mercy CH Chub O'Reilly Cancer Center โ Springfield, Missouri
- The Alvin J. Siteman Cancer Center - Center for Advanced Med โ St Louis, Missouri
- Mercy David C. Pratt Cancer Center - St. - Mercy Research - David C. Pratt Cancer Center โ St Louis, Missouri
- Saint Joseph Hospital - Cancer Centers - St. Vincent Frontier Cancer Center โ Billings, Montana
- Dartmouth Hitchcock Medical Center โ Lebanon, New Hampshire
- Memorial Sloan Kettering - Hackensack - Memorial Sloan Kettering Basking Ridge โ Basking Ridge, New Jersey
๐ Contact the Study Coordinator
Phone: (800) 888-7704
Email: Astellas.registration@astellas.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ 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.
More studies in Pancreatic Cancer
- A Study of the Life Changes Experienced by Patients With Pancreatic Cancer โ New York, New York
- Boost GVAX Pancreas Vaccine With or Without CY in Patients With Pancreas Cancer โ Baltimore, Maryland
- Study Of Gemcitabine, Nab-paclitaxel, PEGPH20 and Rivaroxaban for Advanced Pancreatic Adenocarcinoma โ Hartford, Connecticut
- Pulse-low-dose Rate (PLDR) Radiation in Pancreatic Cancer โ Philadelphia, Pennsylvania
- Use of High-dose Radiation Therapy Plus Chemotherapy to Improve the Likelihood of Surgical Treatment in Patients With Locally Advanced Pancreatic Cancer โ Basking Ridge, New Jersey
- Platform Study of Neoadjuvant and Adjuvant Immunotherapy for Patients With Resectable Adenocarcinoma of the Pancreas โ Baltimore, Maryland
Explore by condition: All Pancreatic Cancer clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.