drugset / Trial / NCT01293006

Effects of Suvorexant in Patients With Chronic Obstructive Pulmonary Disease (MK-4305-032)

NCT01293006

Phase 1 Completed 25 enrolled Merck Sharp & Dohme LLC
RandomizedCrossoverDouble-blindTreatment

Summary

This study will evaluate the safety, tolerability, and effect of multiple doses of suvorexant (MK-4305) on respiratory function in participants with chronic obstructive pulmonary disease (COPD). This is a crossover study, so all participants will receive both suvorexant and placebo while on study. The primary hypothesis of this study is that multiple doses of suvorexant do not produce a clinically significant reduction of mean oxygen saturation (SaO2) during total sleep time in participants with COPD, as compared to placebo.

Timeline

Start
2011-03-25
Primary completion
2012-01-20
Completion
2012-02-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Suvorexant Small molecule 30 mg Oral
Subject Suvorexant Small molecule 40 mg Oral

Indications