RESPONSE: Response to Seladelpar in Subjects With Primary Biliary Cholangitis (PBC) and an Inadequate Control to or an Intolerance to Ursodeoxycholic Acid (UDCA)

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

RESPONSE: A PLACEBO-CONTROLLED, RANDOMIZED, PHASE 3 STUDY TO EVALUATE THE SAFETY AND EFFICACY OF SELADELPAR IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS (PBC) AND AN INADEQUATE RESPONSE TO OR AN INTOLERANCE TO URSODEOXYCHOLIC ACID (UDCA)

Intervention/treatment:
SELADELPAR (MBX-8025)
Medical condition:
PRIMARY BILIARY CHOLANGITIS (PBC)
Protocol code:
CB8025-32048
Control number:
249166
Status:
Closed
Approved:
March 03, 2021
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04620733
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
CymaBay Study Director
Organization
CymaBay Therapeutics, Inc.
Phone:
1-510-293-8800
Sponsor
CYMABAY THERAPEUTICS INC

Locations

Ontario

London Health Sciences Centre
London, Ontario, N6A 5A5
Toronto Digestive Disease Associates Inc
Vaughan, Ontario, L4L 4Y7
University Health Network
Toronto, Ontario, M5G 2C4

Results

See the results from the trial NCT04620733. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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