A Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of EDP-305 in Subjects With Primary Biliary Cholangitis

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE 2 DOSE RANGING, RANDOMIZED, DOUBLE BLIND, PLACEBO-CONTROLLED STUDY EVALUATING THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY OF EDP-305 IN SUBJECTS WITH PRIMARY BILIARY CHOLANGITIS (PBC) WITH OR WITHOUT AN INADEQUATE RESPONSE TO URSODEOXYCHOLIC ACID (UDCA)

Intervention/treatment:
EDP-305
Medical condition:
PRIMARY BILIARY CHOLANGITIS (PBC)
Protocol code:
EDP 305-201
Control number:
216805
Status:
Closed
Approved:
June 28, 2018
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT03394924
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 75 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Nathalie Adda
Organization
Enanta Pharmaceuticals, Inc.
Phone:
+1 6176070705
Sponsor
ENANTA PHARMACEUTICALS INC

Locations

Ontario

London Health Sciences Centre University Hospital
London, Ontario, N6A 5A5
Toronto General Hospital
Toronto, Ontario, M5G 2C4
Toronto Liver Center
Toronto, Ontario, M6H 3M1

Results

See the results from the trial NCT03394924. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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