RecruitingPhase 3NCT07409272

A Study to Evaluate the Effectiveness and Safety of Setidegrasib, Given With Either mFOLFIRINOX or NALIRIFOX Chemotherapies, in People With Pancreatic Cancer

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


Sponsor

Astellas Pharma Global Development, Inc.

Enrollment

614 participants

Start Date

Feb 17, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

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. 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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether adding a new targeted drug called setidegrasib to standard chemotherapy (mFOLFIRINOX or NALIRIFOX) works better than chemotherapy alone for people with metastatic pancreatic cancer that has a specific genetic mutation called KRAS G12D. **You may be eligible if...** - You are an adult with confirmed metastatic pancreatic ductal adenocarcinoma (pancreatic cancer that has spread) - Your tumor has been tested and found to have a KRAS G12D mutation - Your cancer cannot be treated with surgery or curative radiation - You have not yet received chemotherapy for metastatic disease (except up to 2 doses during screening) - You are in good overall health (ECOG 0 or 1) - Your organ function (blood, liver, kidneys) is adequate **You may NOT be eligible if...** - You have had prior treatment with a KRAS G12D-targeted agent - You have chronic inflammatory bowel disease or severe diarrhea - You have significant nerve damage affecting your function - You have active fluid collections (ascites or pleural effusion) requiring drainage procedures - You have a history of interstitial lung disease or pulmonary fibrosis - You have a recent heart attack, unstable angina, or uncontrolled heart failure - You have uncontrolled seizures Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSetidegrasib

Intravenous infusion

DRUGOxaliplatin

Intravenous infusion

DRUGLeucovorin

Intravenous infusion

DRUGIrinotecan

Intravenous infusion

DRUGfluorouracil

Intravenous infusion

DRUGliposomal irinotecan

Intravenous infusion

DRUGPlacebo

Intravenous Infusion


Locations(13)

Crosson Cancer Institute at Providence St. Jude Medical Center in Fullerton

Fullerton, California, United States

Baptist MD Anderson Cancer Institute

Jacksonville, Florida, United States

Saint Elizabeth Medical Center, Inc. DBA St. Elizabeth Health Care

Edgewood, Kentucky, United States

HealthPartners Frauenshuh Cancer Center

Saint Louis Park, Minnesota, United States

HealthPartners Cancer Center at Regions Hospital

Saint Paul, Minnesota, United States

NYU Long Island Mineola

Mineola, New York, United States

Laura and Isaac Perlmutter Cancer Center at NYU Langone

New York, New York, United States

White Plains Hospital Center for Cancer Care - Oncology

White Plains, New York, United States

Utah Cancer Specialists

Salt Lake City, Utah, United States

UVA Emily Couric Cancer Center

Charlottesville, Virginia, United States

Virginia Cancer Specialists

Fairfax, Virginia, United States

Virginia Mason Franciscan Health - Virginia Mason Medical Center

Seattle, Washington, United States

The University of Tokyo Hospital

Bunkyo-ku, Tokyo, Japan

View Full Details on ClinicalTrials.gov

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NCT07409272


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