Clin2
NCT06443606Possibly a fitRecruiting

Bezafibrate for primary biliary cholangitis with incomplete UDCA response

BPCNon Optimal Response to UDCA

Treatments studied

Part of Digestive system clinical trials.

This trial tests if adding bezafibrate (200 mg or 400 mg) to standard UDCA treatment can improve liver function in people with primary biliary cholangitis whose UDCA alone isn't working well enough.

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

Phase
Phase 3
Enrollment
108 people
Ages
18 years to 80 years
Study type
Interventional

Who can take part

  • Age 18 to 79 years old
  • Diagnosed with primary biliary cholangitis (PBC)
  • Been on UDCA for at least 12 months, with a stable dose for the last 3 months
  • PBC not well controlled on UDCA alone (based on certain blood test results)

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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