Pancreatic Cancer Trial, Recruiting NCT06228599 Sponsor: Medical College of Wisconsin Condition: Pancreatic Cancer
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Pancreatic Cancer Trial, Recruiting

NCT06228599
Recruiting Not Applicable

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:

  • Adults aged 18 or older
  • People who have been diagnosed with pancreatic cancer confirmed by a laboratory test (not the neuroendocrine type)
  • People whose pancreatic tumor has been surgically removed, and who have either received additional treatments such as chemotherapy or radiation before or after surgery, or who were not able to or chose not to receive those additional treatments
  • People who have at least one of the following: a blood marker called CA 19-9 that is elevated (above 35 U/mL, measured at least 6 weeks after surgery, with a normal bilirubin level), or cancer features found during surgery that suggest a higher risk of return, such as cancer cells found at the edges of the removed tissue or in nearby lymph nodes
  • People who have no clear signs of cancer returning or spreading at the time of their first scan after surgery (or within four weeks of an elevated CA 19-9 result)
  • People whose blood test results meet certain minimums for white blood cell counts, platelets, red blood cells, and liver enzyme levels (confirm with trial site for specific values)
  • People who are well enough to carry out basic daily activities — specifically, those with an ECOG performance score below 3, meaning they are not completely bedridden (confirm with trial site)
  • People who have stopped taking other cancer-fighting treatments for a required period of time before the trial begins
  • People who are able to swallow and keep down oral medications, if required by the assigned treatment
  • People who are not pregnant, not breastfeeding, and willing to use effective contraception during the study and for at least one month after treatment ends — this applies to both female and male participants, with specific requirements for each group (confirm with trial site for full details)
  • People whose case has been reviewed by a Molecular Tumor Board (a specialist panel) and who agree to follow the treatment that panel recommends
  • People who are able to understand and are willing to sign a written consent form

Who may not be able to join:

  • People whose body does not naturally produce the CA 19-9 marker, unless they have high-risk surgical findings (such as cancer at the surgical margins or in lymph nodes)
  • People who are currently taking another experimental treatment for pancreatic cancer
  • People whose scans show that the cancer has already spread to other parts of the body
  • People who are unable to swallow medications
  • People who are having more than 6 episodes of diarrhea per day after surgery, even with maximum medical treatment
  • People who have an active infection (bacterial, viral, or fungal) that currently requires intravenous (IV) antibiotic or antifungal treatment
  • People who have had a major surgical procedure (other than a simple diagnostic biopsy) within four weeks before the trial start date, or who have a major surgery planned in that window
  • People who have a known allergy or sensitivity to any of the study drugs or their ingredients
  • People with serious uncontrolled health conditions, such as unstable chest pain (angina), a significant uncontrolled heart rhythm problem, or mental health or personal circumstances that would make it difficult to follow the trial requirements
  • People who are pregnant, breastfeeding, or of childbearing potential and not using adequate contraception

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Mandana Kamgar, MD, MPH, 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

Status
Recruiting
Phase
Not Applicable
Sponsor
Medical College of Wisconsin
Registry
ClinicalTrials.gov
Start date
29 February 2024
Est. completion
31 January 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Disease-free Survival; Adverse Events

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov