Clin2
NCT07350070Possibly a fitNot yet recruiting

Combination therapy for liver cancer with portal hypertension

HCCLiver CirrhosisPortal Hypertension

Part of Digestive system clinical trials.

This study tests a combination therapy for liver cancer that cannot be surgically removed. It includes a procedure called TACE (which blocks the tumor's blood supply), along with targeted therapy (lenvatinib), immunotherapy (tislelizumab), and a blood pressure medicine (carvedilol) that may also help the liver. The goal is to see if this combination is safe and effective for people who also have high blood pressure in the liver's blood vessels.

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

Phase
Phase 2
Enrollment
78 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • You are between 18 and 75 years old.
  • You have been newly diagnosed with liver cancer that has not been treated before.
  • You have at least one tumor that can be seen on a CT or MRI scan (at least 1 cm across).
  • Your liver function is relatively good (Child-Pugh score 7 or less, meaning no fluid in the belly or confusion).
  • You have evidence of increased blood pressure in the liver's blood vessels (portal hypertension) — for example, enlarged veins in the stomach or esophagus, or high liver stiffness on a special test.
  • You are generally able to take care of yourself (ECOG score 0 or 1).

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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