Phase 3 Primary Biliary Cholangitis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You must be willing and able to sign and date a consent form agreeing to take part in the study
- You must have previously taken part in the fenofibrate study for PBC (a specific earlier clinical trial, reference NCT02823353)
- If you are a woman who could become pregnant, you must agree to use at least one barrier method of contraception (such as a condom or diaphragm) plus one additional form of birth control during the study and for at least 90 days after your last dose
- If you are a man who is sexually active with a woman who could become pregnant, you must use a barrier method of contraception, and your partner must also use an additional form of birth control during the study and for at least 90 days after the last dose
Who may not be able to join:
- You had to stop taking fenofibrate during the previous study because of a side effect from the treatment
- You have another serious health condition (such as cancer) that, in the doctor's opinion, would prevent you from fully taking part in the study or affect the results
- You have a known history of other liver diseases (besides PBC)
- You are currently pregnant or breastfeeding (for women)
- You have been taking immune-suppressing medications long-term
- You have any other condition that the study doctor believes could put your safety at risk or affect the quality of the study results (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +862984771539
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Treatment emergent adverse events (TEAEs); Percentage of patients with biochemical response
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.