drugset / Trial / NCT00597818
Cobiprostone Prevention of NSAID-induced Gastroduodenal Injury
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The primary purpose of this study is to determine the efficacy and safety of three dose levels of cobiprostone as compared to placebo in OA/RA patients treated with an NSAID for 20 months.
Timeline
- Start
- 2007-08
- Primary completion
- 2009-04
- Completion
- 2009-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cobiprostone | Small molecule | 18 ug | Oral |