Study of OCA in Combination With BZF Evaluating Efficacy, Safety and Tolerability in Participants With PBC

Last updated:
2026-07-25
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View trial details

Overview

Official protocol title:

A PHASE 2A, DOUBLE-BLIND, RANDOMIZED, ACTIVE CONTROLLED, PARALLEL GROUP STUDY EVALUATING THE EFFICACY, SAFETY, AND TOLERABILITY OF BEZAFIBRATE ADMINISTERED IN COMBINATION WITH OBETICHOLIC ACID IN SUBJECTS WITH PRIMARY BILIARY CHOLANGITIS

Intervention/treatment:
OBETICHOLIC ACID / BEZAFIBRATE
Medical condition:
PRIMARY BILIARY CHOLANGITIS (PBC)
Protocol code:
747-214
Control number:
261743
Status:
Closed
Approved:
March 25, 2022
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT05239468
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Medical Information
Organization
Intercept Pharmaceuticals, Inc.
Phone:
844-782-4278
Sponsor
INTERCEPT PHARMACEUTICALS INC

Locations

Alberta

The Northern Alberta Clinical Trials and Research Centre
Edmonton, Alberta, T6G 287

British Columbia

Pacific Gastroenterology Associates
Vancouver, British Columbia, V6Z 2K5

Quebec

University of Montreal
Montreal, Quebec, V6Z 2K5

Results

See the results from the trial NCT05239468. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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