Clin2
NCT07592819Possibly a fitNot yet recruiting

Personalized chemotherapy for borderline pancreatic cancer

Pancreas Adenocarcinoma (MSI-H)Pancreatic Cancer Resectable

Treatments studied

Part of Cancer clinical trials.

This trial tests a personalized approach to chemotherapy for people with borderline-resectable pancreatic cancer. It uses a lab test to find out if the cancer is likely to respond to a standard drug (gemcitabine), and if not, gives a different chemotherapy combination that might work better.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
367 people
Ages
18 years to 80 years
Study type
Interventional

Who can take part

  • You have borderline-resectable pancreatic ductal adenocarcinoma (a type of pancreatic cancer that is on the edge of being removable by surgery).
  • Your cancer was confirmed by a biopsy (tissue sample).
  • You are generally in good health (able to care for yourself and do daily activities).
  • You have not had chemotherapy, radiation, or surgery for pancreatic cancer before (except one dose of a chemotherapy called mFOLFIRINOX while waiting for the test result).
  • You are between 18 and 80 years old (if 75–80, a special health assessment is needed).
  • You are enrolled in the PRODIGE 104 A NEOPREDICT study and your cancer tested negative for a gemcitabine sensitivity signature (a lab test showing the drug is less likely to work).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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