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N/A N=4,577

Real-World Data Study to Evaluate the Effectiveness of OCA on Hepatic Outcomes in PBC Patients

Primary Biliary Cholangitis

Enrolled (actual)
4,577
Serious AEs
Results posted
Jan 2025
Primary outcome: Primary: Risk of the First Event of the Composite Events — 8; 32 Events during the study period — p=<.001

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Intercept Pharmaceuticals
Primary completion
Dec 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Risk of the First Event of the Composite Events
8; 32 <.001 sig
SECONDARY
Risk of Death
2; 9
SECONDARY
Risk of Liver Transplantation
2; 12
SECONDARY
Risk of Hospitalization for Hepatic Decompensation
6; 23

Summary

This is an observational, retrospective cohort study of patients with primary biliary cholangitis (PBC) who failed ursodeoxycholic acid (UDCA) treatment, using a real-world data source, the Komodo Health United States (US) claims database. The study is designed to evaluate the effectiveness of obeticholic acid (OCA). All patients who meet diagnostic criteria for PBC in the database between 01 Jun 2015 and 31 Dec 2021 and who meet all eligibility criteria were considered for this study.

Eligibility Criteria

Key Inclusion Criteria

  • Definite or probable PBC diagnosis
  • Inadequate response or intolerance to UDCA
  • Age ≥18 years at the index date
  • Continuous enrollment and evaluable data for at least 12 months before the index date (inclusive)

Key Exclusion Criteria

  • History or presence of other concomitant liver diseases
  • History of non-skin malignancy or melanoma
  • History of HIV
  • Medical conditions that may cause non-hepatic increases in ALP
  • Patients with laboratory values indicative of hepatic decompensation or significant hepatobiliary injury
  • History of liver transplant
  • Evidence of fenofibrate, or bezafibrate use
  • History or presence of hepatic decompensating events
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05292872). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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