Phase 3 Primary Biliary Cholangitis Trial, Recruiting NCT06365424 Sponsor: Xijing Hospital of Digestive Diseases Condition: Primary Biliary Cholangitis
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Phase 3 Primary Biliary Cholangitis Trial, Recruiting

NCT06365424
Recruiting Phase 3

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 3
Sponsor
Xijing Hospital of Digestive Diseases
Registry
ClinicalTrials.gov
Start date
8 April 2017
Est. completion
1 April 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Treatment emergent adverse events (TEAEs); Percentage of patients with biochemical response

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov