drugset / Trial / NCT01293006
Effects of Suvorexant in Patients With Chronic Obstructive Pulmonary Disease (MK-4305-032)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Suvorexant | Small molecule | 30 mg | Oral |
| Subject | Suvorexant | Small molecule | 40 mg | Oral |