drugset / Trial / NCT00588302

Moexipril for Primary Biliary Cirrhosis

NCT00588302

Phase 2 Completed 20 enrolled Mayo Clinic UCB Pharma · collab
NaSingle-groupOpen-labelTreatment

Summary

The blockade of angiotensin II synthesis attenuates hepatic fibrosis in different experimental models of chronic liver injury. We aimed to determine the safety and efficacy of moexipril, an angiotensin-converting enzyme (ACE) inhibitor, on liver biochemistries, Mayo risk score, and health-related quality of life in patients with primary biliary cirrhosis (PBC) who have had a suboptimal response to ursodeoxycholic acid (UDCA).

Timeline

Start
2003-06
Primary completion
2007-06
Completion
2007-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Moexipril Small molecule 15 mg Oral