drugset / Trial / NCT01300455
Effects of Suvorexant in Participants With Obstructive Sleep Apnea (MK-4305-036)
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 mild to moderate obstructive sleep apnea (OSA) compared to administration of placebo. The primary hypothesis of this study is that multiple doses of MK-4305 do not produce a clinically significant increase in Apnea-Hypopnea Index (AHI) in participants with mild to moderate OSA, as compared to placebo.
Timeline
- Start
- 2011-03-19
- Primary completion
- 2011-08-11
- Completion
- 2011-08-11
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Suvorexant | Small molecule | 40 mg | Oral |