Overview

Study of INT 747 in Combination With URSO in Patients With Primay Biliary Cirrhosis (PBC)

Status:
Completed
Trial end date:
2010-12-01
Target enrollment:
Participant gender:
Summary
The primary hypothesis is that INT-747 will cause a reduction in alkaline phosphatase levels in Primary Biliary Cirrhosis patients, over a 12 week treatment period, as compared to placebo.
Phase:
Phase 2
Details
Lead Sponsor:
Intercept Pharmaceuticals
Treatments:
Chenodeoxycholic Acid
Ursodeoxycholic Acid