Clin2
NCT07128290Possibly a fitNot yet recruiting

Combination treatment before and after surgery for high-risk bile duct cancer

Intrahepatic Cholangiocarcinoma (Icc)

Part of Cancer clinical trials.

This trial tests a new drug combination—cisplatin, gemcitabine (standard chemotherapy), and rilvegostomig (an immunotherapy)—given before and after surgery for a specific type of liver cancer called intrahepatic cholangiocarcinoma. The goal is to reduce the chance of the cancer coming back after surgery.

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

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

Who can take part

  • You are 18 years of age or older.
  • You have been diagnosed with intrahepatic cholangiocarcinoma (bile duct cancer that starts in the liver).
  • Your cancer has at least one high-risk feature (such as being larger than 5 cm, having multiple liver tumors, or having cancer in blood vessels or nearby lymph nodes).
  • Your cancer is considered removable with surgery, and you have not had any prior treatment for it.
  • Your overall health is good (able to do most daily activities), and your organs (like kidneys and liver) are working well enough.
  • You do not have cirrhosis with severe liver damage, uncontrolled infections, or other active cancers.

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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