Clinical trial
A Phase 2, Double-Blind, Randomized, Parallel Group Study Evaluating the Efficacy, Safety, and Tolerability of Obeticholic Acid Administered in Combination With Bezafibrate in Subjects With Primary Biliary Cholangitis Who Had an Inadequate Response or Who Were Unable to Tolerate Ursodeoxycholic Acid
NCT04594694 is registered in ClinicalTrials.gov with Intercept Pharmaceuticals as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 2, Double-Blind, Randomized, Parallel Group Study Evaluating the Efficacy, Safety, and Tolerability of Obeticholic Acid Administered in Combination With Bezafibrate in Subjects With Primary Biliary Cholangitis Who Had an Inadequate Response or Who Were Unable to Tolerate Ursodeoxycholic Acid
- Lead sponsor
- Intercept Pharmaceuticals
- Phase
- Phase 2
- Overall status
- Terminated
- Start date
- October 2, 2019
- Completion date
- October 14, 2025
- Enrollment
- 75 (actual)
- Sites
- 33
Conditions
As the registry lists them; a condition with its own page is linked.
primary biliary cholangitis