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Generated: December 18, 2018

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CLINICAL TRIALS PROFILE FOR BELSOMRA

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Clinical Trials for Belsomra

Trial ID Title Status Sponsor Phase Summary
NCT02491788 Examination of the Effectiveness of Suvorexant in Improving Daytime Sleep in Shift Workers Recruiting Merck Sharp & Dohme Corp. Phase 4 The purpose of this study is to test the hypothesis that ingestion of the wake-inhibiting drug suvorexant 30 minutes prior to daytime sleep initiation in individuals working overnight shifts will significantly improve both objective (total sleep time, sleep efficiency, wake after sleep onset) and subjective (sleep quality) measures of daytime sleep.
NCT02491788 Examination of the Effectiveness of Suvorexant in Improving Daytime Sleep in Shift Workers Recruiting Stanford University Phase 4 The purpose of this study is to test the hypothesis that ingestion of the wake-inhibiting drug suvorexant 30 minutes prior to daytime sleep initiation in individuals working overnight shifts will significantly improve both objective (total sleep time, sleep efficiency, wake after sleep onset) and subjective (sleep quality) measures of daytime sleep.
NCT02491788 Examination of the Effectiveness of Suvorexant in Improving Daytime Sleep in Shift Workers Recruiting VA Palo Alto Health Care System Phase 4 The purpose of this study is to test the hypothesis that ingestion of the wake-inhibiting drug suvorexant 30 minutes prior to daytime sleep initiation in individuals working overnight shifts will significantly improve both objective (total sleep time, sleep efficiency, wake after sleep onset) and subjective (sleep quality) measures of daytime sleep.
NCT02527564 Efficacy of Suvorexant to Treat Insomnia Related to Bipolar Disorder Recruiting Merck Sharp & Dohme Corp. Phase 4 The purpose of this study is to evaluate the efficacy of suvorexant, added to existing medications, for treatment-resistant insomnia in individuals with bipolar disorder. The investigators hypothesize that participants receiving suvorexant for one week will experience significantly greater improvement in sleep duration compared to participants receiving placebo.
NCT02527564 Efficacy of Suvorexant to Treat Insomnia Related to Bipolar Disorder Recruiting Stanford University Phase 4 The purpose of this study is to evaluate the efficacy of suvorexant, added to existing medications, for treatment-resistant insomnia in individuals with bipolar disorder. The investigators hypothesize that participants receiving suvorexant for one week will experience significantly greater improvement in sleep duration compared to participants receiving placebo.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Belsomra

Condition Name

Condition Name for Belsomra
Intervention Trials
Insomnia 9
Posttraumatic Stress Disorder 2
MDD 1
Amyloid-beta 1
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Condition MeSH

Condition MeSH for Belsomra
Intervention Trials
Sleep Initiation and Maintenance Disorders 10
Stress Disorders, Post-Traumatic 2
Disease 2
Sleep Wake Disorders 2
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Clinical Trial Locations for Belsomra

Trials by Country

Trials by Country for Belsomra
Location Trials
United States 11
Canada 1
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Trials by US State

Trials by US State for Belsomra
Location Trials
Washington 2
California 2
Pennsylvania 1
Missouri 1
Massachusetts 1
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Clinical Trial Progress for Belsomra

Clinical Trial Phase

Clinical Trial Phase for Belsomra
Clinical Trial Phase Trials
Phase 4 11
Phase 2/Phase 3 1
Phase 2 1
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Clinical Trial Status

Clinical Trial Status for Belsomra
Clinical Trial Phase Trials
Recruiting 10
Not yet recruiting 4
Enrolling by invitation 1
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Clinical Trial Sponsors for Belsomra

Sponsor Name

Sponsor Name for Belsomra
Sponsor Trials
Merck Sharp & Dohme Corp. 6
Stanford University 2
Howard University 2
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Sponsor Type

Sponsor Type for Belsomra
Sponsor Trials
Other 19
Industry 8
U.S. Fed 1
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Serving hundreds of leading biopharmaceutical companies globally:

Medtronic
Accenture
Covington
Express Scripts
AstraZeneca
McKesson
UBS
Johnson and Johnson
Fish and Richardson

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