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Enrolling by Invitation

NCT Number: NCT06591468

A Multicenter, Randomized, Controlled Trial of Prednisone Combined With Ursodeoxycholic Acid in the Treatment of Primary Biliary Cholangitis With Moderate to Severe Interface Hepatitis Characteristics

About 1/3 of patients with primary biliary cholangitis (PBC) exhibit moderate to severe interface hepatitis, and this group of patients have poor response to UDCA treatment. However, as it is not yet sufficient to diagnose autoimmune hepatitis or overlap syndrome, it is difficult to initiate immunosuppressive therapy such as steroids according to current guidelines. The aim of this study is to explore whether PBC patients with moderate to severe interfacial inflammation can benefit from UDCA combined with prednisone therapy, and its treatment safety.

Enrolling by Invitation

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Sun Yat-sen Memorial Hospital, Guangzhou, Guangdong, China

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Voluntarily joining the group, able to understand and sign an informed consent form;
  • 18 years old ≤ age ≤ 75 years old;
  • The diagnosis of primary biliary cholangitis follows the AASLD international diagnostic and treatment guidelines (meeting two of the following three criteria: AMA or gp210, sp100 positive; Elevated serum ALP levels; Pathological manifestations include non suppurative cholangitis and destruction of the interlobular bile duct;
  • Liver histology suggests moderate to severe interfacial hepatitis (moderate,<50% portal or fibrous septa destruction, severe,>50% portal or fibrous septa destruction) with serum ALT<5 * ULN, serum IgG<2 * ULN, and negative serum anti smooth muscle antibodies;
  • Not receiving UDCA, hormone or other immunosuppressive therapy before enrollment;
  • ALP>1.67 * ULN.

Exclusion criteria

  • History or presence of other concomitant liver diseases.
  • ALT or AST > 5×ULN, TBIL > 3×ULN.
  • If female: known pregnancy, or has a positive urine pregnancy test (confirmed by a positive serum pregnancy test), or lactating.
  • Allergic to fenofibrate or ursodeoxycholic acid.
  • Taking hepatotoxic drugs (e.g., dapsone, erythromycin, fluconazole, ketoconazole, rifampicin) for more than 2 weeks within 6 months, and long-term hormonal users.
  • Recurrent variceal bleeding, poorly controlled hepatic encephalopathy or refractory ascites.
  • Patients with a history of severe cardiac, cerebrovascular, renal, respiratory disease or functional failure, and psychiatric disorders (including those due to alcohol and drug abuse).
  • Creatinine >1.5×ULN and creatinine clearance <60 ml/min.
  • Currently using statins (such as pravastatin, fluvastatin, and simvastatin), other fibrates (such as gemfibrozil and bezafibrate), and drugs structurally similar to fenofibrate (like ketoprofen).
  • Planned to receive an organ transplant or an organ transplant recipient.
  • Needing Liver transplantation within 1 year according to the Mayo Rick score.
  • Any other condition(s) that would compromise the safety of the subject or compromise

Treatment and study plan

Prednisone

Drug

Prednisone 30-40 mg/day, at 7am in the morning, gradually reduced after 1 month (5mg every 7-14 days) to 5-10 mg for maintenance treatment

UDCA (Ursodeoxycholic acid)

Drug

13-15 mg/kg/day

Primary outcomes

  1. Percentage of patients with biochemical response

    Time frame: 1 year

    Alkaline Phosphatase &lt; 1.67*ULN

Secondary outcomes

  1. Assessment of the pruritus and fatigue

    Time frame: 1, 3, 6, 9, and 12 months

    Change From Baseline in Fatigue and Pruritus as Assessed by Visual Analogue Scale (VAS) Total Score for Fatigue and Pruritus. (0-10, higher scires mean a worse outcome)

  2. Survival without transplantation and hepatic impairment

    Time frame: 1 year

    Occurrence of ascites, variceal bleeding, hepatic encephalopathy, liver-transplantation, or death.

Sponsors and collaborators

Lead sponsor

Han Ying

Other

Registry information

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Sep 19, 2024
Registry last updated
Nov 28, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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