drugset / Trial / NCT00737594
Efficacy and Safety of Cobiprostone in Patients With Portal Hypertension
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cobiprostone | Small molecule | 12 ug | Oral |
| Subject | Cobiprostone | Small molecule | 18 ug | Oral |