drugset / Trial / NCT01300455

Effects of Suvorexant in Participants With Obstructive Sleep Apnea (MK-4305-036)

NCT01300455

Phase 1 Completed 26 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 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

EvaluationDrugModalityDoseRoute
Subject Suvorexant Small molecule 40 mg Oral