drugset / Trial / NCT02177136

Obeticholic Acid (OCA) in Primary Sclerosing Cholangitis (PSC)

NCT02177136

Phase 2 Completed 77 enrolled Intercept Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

This was a phase 2, double-blind (DB), placebo-controlled trial in participants with primary sclerosing cholangitis to evaluate the effect of obeticholic acid on liver biochemistry, in particular, serum alkaline phosphatase; and, safety. The long-term safety extension (LTSE) phase was conducted to evaluate the safety, tolerability, and efficacy of long-term, open-label use of OCA in participants with PSC who had completed the DB phase of the study.

Timeline

Start
2015-02-09
Primary completion
2017-03-07
Completion
2018-03-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Obeticholic Acid Small molecule 3 mg Oral
Subject Obeticholic Acid Small molecule 10 mg Oral