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Last Updated: May 24, 2024

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CLINICAL TRIALS PROFILE FOR BELSOMRA


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All Clinical Trials for Belsomra

Trial ID Title Status Sponsor Phase Start Date Summary
NCT02491788 ↗ Examination of the Effectiveness of Suvorexant in Improving Daytime Sleep in Shift Workers Completed Merck Sharp & Dohme Corp. Phase 4 2016-02-01 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 Completed Stanford University Phase 4 2016-02-01 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 Completed VA Palo Alto Health Care System Phase 4 2016-02-01 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 2015-09-01 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 >Phase >Start Date >Summary

Clinical Trial Conditions for Belsomra

Condition Name

Condition Name for Belsomra
Intervention Trials
Insomnia 16
Alcohol Use Disorder 2
Sleep 2
Sleep Disorder 2
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Condition MeSH

Condition MeSH for Belsomra
Intervention Trials
Sleep Initiation and Maintenance Disorders 20
Sleep Wake Disorders 7
Parasomnias 6
Disease 5
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Clinical Trial Locations for Belsomra

Trials by Country

Trials by Country for Belsomra
Location Trials
United States 30
Japan 1
Australia 1
Canada 1
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Trials by US State

Trials by US State for Belsomra
Location Trials
California 5
Massachusetts 4
Michigan 4
Maryland 3
Washington 2
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Clinical Trial Progress for Belsomra

Clinical Trial Phase

Clinical Trial Phase for Belsomra
Clinical Trial Phase Trials
Phase 4 20
Phase 2/Phase 3 1
Phase 2 8
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Clinical Trial Status

Clinical Trial Status for Belsomra
Clinical Trial Phase Trials
Recruiting 13
Completed 8
Not yet recruiting 6
[disabled in preview] 2
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Clinical Trial Sponsors for Belsomra

Sponsor Name

Sponsor Name for Belsomra
Sponsor Trials
Merck Sharp & Dohme Corp. 8
Henry Ford Health System 3
Stanford University 3
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Sponsor Type

Sponsor Type for Belsomra
Sponsor Trials
Other 41
Industry 12
NIH 5
[disabled in preview] 4
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