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Last Updated: October 20, 2019

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CLINICAL TRIALS PROFILE FOR BELSOMRA

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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 Recruiting 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 Recruiting 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 Recruiting 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.
NCT02527564 Efficacy of Suvorexant to Treat Insomnia Related to Bipolar Disorder Recruiting Stanford University 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.
NCT02669030 A Six Week, Randomized, Double-Blind Placebo-Controlled, Suvorexant Augmentation Study of Antidepressant Treatment of Major Depressive Disorder With Residual Insomnia Not yet recruiting Jefferson Medical College of Thomas Jefferson University Phase 4 2016-02-01 Depression with ongoing insomnia is a common clinical presentation with patients. Clinical data suggests that patients with insomnia that receive concomitant treatment with a sleep aid experience a more robust antidepressant response along with a quicker response. The purpose of this clinical study is to compare the effectiveness of the FDA-approved insomnia medication suvorexant, also known as Belsomra®, as add-on treatment to an antidepressant to that of placebo plus antidepressant treatment in patients with depression and residual or ongoing insomnia.
NCT02669030 A Six Week, Randomized, Double-Blind Placebo-Controlled, Suvorexant Augmentation Study of Antidepressant Treatment of Major Depressive Disorder With Residual Insomnia Not yet recruiting Medical College of Georgia at Augusta University, Department of Psychiatry and Health Behavior, Augusta, GA Phase 4 2016-02-01 Depression with ongoing insomnia is a common clinical presentation with patients. Clinical data suggests that patients with insomnia that receive concomitant treatment with a sleep aid experience a more robust antidepressant response along with a quicker response. The purpose of this clinical study is to compare the effectiveness of the FDA-approved insomnia medication suvorexant, also known as Belsomra®, as add-on treatment to an antidepressant to that of placebo plus antidepressant treatment in patients with depression and residual or ongoing insomnia.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Belsomra

Condition Name

Condition Name for Belsomra
Intervention Trials
Insomnia 13
Bipolar Disorder 2
Posttraumatic Stress Disorder 2
Sleep Initiation and Maintenance Disorders 2
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Condition MeSH

Condition MeSH for Belsomra
Intervention Trials
Sleep Initiation and Maintenance Disorders 16
Sleep Wake Disorders 6
Parasomnias 6
Disease 4
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Clinical Trial Locations for Belsomra

Trials by Country

Trials by Country for Belsomra
Location Trials
United States 17
Canada 1
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Trials by US State

Trials by US State for Belsomra
Location Trials
California 4
Washington 2
Michigan 2
Maryland 1
Illinois 1
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Clinical Trial Progress for Belsomra

Clinical Trial Phase

Clinical Trial Phase for Belsomra
Clinical Trial Phase Trials
Phase 4 17
Phase 2/Phase 3 1
Phase 2 3
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Clinical Trial Status

Clinical Trial Status for Belsomra
Clinical Trial Phase Trials
Not yet recruiting 12
Recruiting 10
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. 7
Massachusetts General Hospital 2
Stanford University 2
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Sponsor Type

Sponsor Type for Belsomra
Sponsor Trials
Other 29
Industry 9
U.S. Fed 4
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