drugset / Trial / NCT00737594

Efficacy and Safety of Cobiprostone in Patients With Portal Hypertension

NCT00737594 ↗

RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this study is to determine the efficacy and safety of cobiprostone (at two dose levels) as compared to placebo for lowering portal hypertension.

Timeline

Start
2008-07
Primary completion
2009-02
Completion
2009-03

Outcome

Outcome not reported

Stopped (Enrollment): “Failure to enroll a suitable number of qualified subjects.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Cobiprostone Small molecule 12 ug Oral
Subject Cobiprostone Small molecule 18 ug Oral

Indications