Randomized Global Phase 3 Study to Evaluate the Impact on NASH With Fibrosis of Obeticholic Acid Treatment

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE 3, DOUBLE-BLIND, RANDOMIZED, LONG-TERM, PLACEBO-CONTROLLED, MULTICENTER STUDY EVALUATING THE SAFETY AND EFFICACY OF OBETICHOLIC ACID IN SUBJECTS WITH NONALCOHOLIC STEATOHEPATITIS

Intervention/treatment:
OBETICHOLIC ACID (INT-747)
Medical condition:
NONALCOHOLIC STEATOHEPATITIS (NASH)
Protocol code:
747-303
Control number:
188535
Status:
Closed
Approved:
November 10, 2015
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT02548351
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 85 Years
Accepts healthy volunteers: No

Contacts and locations

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

Locations

Centre de Recherche du Centre Hospitalier de l'Universite de Montreal
Montreal, H2X 0A9
GI Research
Edmonton, T5H 4B9
GIRI - GI Research Institute
Vancouver, V6Z 2K5
Gordon and Leslie Diamond Health Care Centre
Vancouver, V5Z 1M9
John Buhler Research Centre
Winnipeg, R3E 3P4
LAIR Centre
Vancouver, V5Z 1H3
PerCuro Clinical Research Ltd.
Victoria, V8V 3M9
The Research Institute of the McGill University Health Centre
Montreal, H4A 3J1
Toronto Center for Liver Disease
Toronto, M5G 2C4
University of Alberta
Edmonton, T6G 2X8
University of Calgary Liver Unit
Calgary, T2N 4Z6

Ontario

London Health Sciences Centre University Hospital
London, Ontario, N6A 5A5
Toronto Liver Centre
Toronto, Ontario, M6H 3M1

Results

See the results from the trial NCT02548351. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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