Clin2
NCT05749822Possibly a fitRecruiting

Fenofibrate for primary biliary cholangitis with stable cirrhosis

Primary Biliary Cholangitis

Treatments studied

Part of Digestive system clinical trials.

This trial studies whether fenofibrate (a cholesterol medicine) can improve outcomes in people with primary biliary cholangitis (PBC) who already take ursodeoxycholic acid (UDCA) but still have abnormal liver blood tests. It specifically looks at people with “compensated” (stable) cirrhosis—meaning the liver disease is present but not causing severe complications right now.

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

Phase
Phase 2/Phase 3
Enrollment
104 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • Be 18 to 75 years old and have a BMI between 17 and 28
  • Have confirmed primary biliary cholangitis (PBC) based on at least two specific test or history findings
  • Have compensated cirrhosis—one or more signs such as imaging/scan findings, endoscopy findings, biopsy results, or certain blood test patterns
  • Have been on UDCA for at least 6 months (with a stable dose for the last 3 months) and still have high ALP blood test results
  • Have no other major liver diseases and no recent serious complications like uncontrolled confusion or hard-to-control fluid in the belly

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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