drugset / Trial / NCT00597818

Cobiprostone Prevention of NSAID-induced Gastroduodenal Injury

NCT00597818 ↗

Phase 2 Completed 121 enrolled Sucampo Pharma Americas, LLC
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

EvaluationDrugModalityDoseRoute
Subject Cobiprostone Small molecule 18 ug Oral