drugset / Trial / NCT00672802

Safety of Ramelteon in Subjects With Mild to Moderate Chronic Obstructive Pulmonary Disease

NCT00672802

Phase 2 Completed 26 enrolled Takeda
RandomizedCrossoverQuadruple-blindTreatment

Summary

This purpose of this study is to assess the safety of ramelteon, once daily (QD), in subjects with chronic obstructive pulmonary disease.

Timeline

Start
2003-08
Primary completion
2004-03
Completion
2004-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Ramelteon Unknown 16 mg Oral