drugset / Trial / 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

NCT06591468

Phase 2/3 Enrolling by invitation 244 enrolled Han Ying
RandomizedParallel-groupOpen-labelTreatment

Summary

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.

Timeline

Start
2024-10-30
Primary completion
2027-12-31
Completion
2027-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Prednisone Other / unclassified 5 mg
Subject Prednisone Other / unclassified 10 mg
Comparator Ursodeoxycholic Acid Small molecule 13 mg/kg
Comparator Ursodeoxycholic Acid Small molecule 15 mg/kg