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NCT07639528Possibly a fitNot yet recruiting

Targeted therapy with chemotherapy for resectable bile duct cancer

Resectable Intrahepatic Cholangiocarcinoma

Treatments studied

Part of Cancer, Digestive system clinical trials.

This study tests a treatment for intrahepatic cholangiocarcinoma (a type of liver cancer) that can be surgically removed. It combines the usual chemotherapy drugs (cisplatin and gemcitabine) with the immunotherapy drug durvalumab, and compares it to the same regimen plus a targeted therapy called futibatinib, which works on specific genetic changes in the tumor. The goal is to see if adding the targeted therapy helps shrink the tumor before surgery and improves the outcome.

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

Phase
Phase 2
Enrollment
44 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have a confirmed diagnosis of intrahepatic cholangiocarcinoma (cancer starting in the bile ducts inside the liver) that is surgically removable and has not spread outside the liver or nearby lymph nodes.
  • You have not had any prior treatment for this cancer (no chemotherapy, radiation, or other therapies).
  • You are at least 18 years old and generally in good health (able to perform most daily activities, as per ECOG status 0-1).
  • You have adequate organ function, which will be checked through blood tests (including kidney, liver, and blood cell counts).
  • You must be able to swallow and take oral medications, and (if applicable) use effective contraception during and for several months after the study.
  • You must not have certain medical conditions, such as uncontrolled heart disease, active eye (corneal or retinal) disorders, or a history of autoimmune disease or high-dose steroids.

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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