drugset / Trial / NCT01097629

Safety and Efficacy Study of Suvorexant in Participants With Primary Insomnia - Study B (MK-4305-029)

NCT01097629

Phase 3 Completed 1020 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a multicenter study to test the hypothesis that suvorexant (MK-4305) is superior to placebo in improving insomnia as measured by change from baseline in: subjective total sleep time and time to sleep onset, wake time after persistent sleep onset, and latency to onset of persistent sleep.

Timeline

Start
2010-05-03
Primary completion
2011-11-08
Completion
2011-11-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Suvorexant Small molecule 15 mg Oral
Subject Suvorexant Small molecule 20 mg Oral
Subject Suvorexant Small molecule 30 mg Oral
Subject Suvorexant Small molecule 40 mg Oral

Indications