Phase 2 Pancreatic Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are suspected of having pancreatic cancer and are scheduled for a procedure (endoscopy) to take a tissue sample for diagnosis.
- You are willing to have a tissue sample taken during an endoscopic procedure for research purposes, or you can provide a previously collected tissue sample for testing.
- You are 18 years of age or older.
- You are able to read and sign a consent form, or you have a legally authorized person who can do this on your behalf.
- Your tissue sample has confirmed a specific type of pancreatic cancer called adenocarcinoma.
- You are generally well enough to carry out daily activities with minimal limitations (confirm with trial site).
- Your cancer has been assessed by CT or MRI scan as either removable by surgery, or borderline removable by surgery, meeting specific criteria about how much the tumor affects nearby blood vessels and other structures (confirm with trial site).
- Your blood counts, kidney function, and liver function meet certain minimum levels as measured by blood tests (confirm with trial site).
- If you are female, you are either past menopause, surgically unable to become pregnant, or have a negative pregnancy test and agree to use contraception before, during, and for four months after treatment.
- If you are male, you are either surgically sterile or agree to use barrier contraception during the study and for four months after your last dose of study medication.
Who may not be able to join:
- You have received chemotherapy or radiation therapy within the past three years.
- You have had another type of cancer within the past three years, unless it was a fully cured skin cancer (basal or squamous cell), fully cured early-stage cervical cancer, or localized prostate cancer with normal PSA levels.
- You have serious uncontrolled health conditions, such as an active serious infection, severe heart problems, uncontrolled irregular heartbeat, significant mental health conditions, a BMI over 55, or anything else that would make it difficult for you to follow the study requirements or give informed consent.
- You have a known infection with HIV, hepatitis B, or hepatitis C.
- You are currently pregnant or breastfeeding, or you are capable of becoming pregnant and are not willing to use contraception starting four weeks before treatment begins.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Kathleen K Christians, MD, Medical College of Wisconsin
Phone: 866-680-0505
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Subjects who receive PurIST classification-directed therapy.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.