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Last Updated: April 3, 2025

CLINICAL TRIALS PROFILE FOR SAREDUTANT


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Clinical Trials for Saredutant

Trial IDTitleStatusSponsorPhaseSummary
NCT00250601 ↗ An Eight-week Study to Evaluate the Efficacy and Safety of Saredutant in Patients With Depression Completed Sanofi Phase 3 The purpose of the study is to evaluate the efficacy and safety of saredutant (or SR48968C) in patients with depression. The primary objective is to evaluate the efficacy of a 100 mg dose of saredutant compared to placebo in patients with depression. The secondary objectives are to evaluate the safety of saredutant, to evaluate the efficacy of saredutant on disability and quality of life in patients with depression, and to evaluate blood levels of saredutant.
NCT00250614 ↗ An Eight-week Study to Evaluate the Efficacy and Safety of Saredutant in Patients With Depression Completed Sanofi Phase 3 The purpose of the study is to evaluate the efficacy and safety of saredutant (or SR48968C) in patients with depression. The primary objective is to evaluate the efficacy of a 100 mg dose of saredutant compared to placebo in patients with depression. The secondary objectives are to evaluate the safety of saredutant, to evaluate the efficacy of saredutant on disability and quality of life in patients with depression, and to evaluate blood levels of saredutant.
NCT00250627 ↗ An Eight-Week Study to Evaluate the Efficacy and Safety of Saredutant in Patients With Depression Completed Sanofi Phase 3 The purpose of the study is to evaluate the efficacy and safety of saredutant (or SR48968C) in patients with depression. The primary objective is to evaluate the efficacy of a 100 mg dose of saredutant compared to placebo in patients with depression. The secondary objectives are to evaluate the safety of saredutant, to evaluate the efficacy of saredutant on disability and quality of life in patients with depression, and to evaluate blood levels of saredutant.
NCT00250653 ↗ A Fifty-two-week Study to Evaluate the Safety of Saredutant in Adult and Elderly Patients With Depression Completed Sanofi Phase 3 The purpose of the study is to evaluate the long-term safety of saredutant (or SR48968C) in adult and elderly patients with depression.The primary objective is to evaluate the long-term safety and tolerability of a 100 mg dose of saredutant in adult and elderly patients with depression. The secondary objective is to evaluate blood levels of saredutant.
NCT00256113 ↗ An Eight-week Study to Evaluate the Efficacy and Safety of Saredutant in Patients With Depression Completed Sanofi Phase 3 The purpose of the study is to evaluate the efficacy and safety of saredutant (or SR48968C) in patients with depression. The primary objective is to evaluate the efficacy of a 100 mg dose of saredutant compared to placebo in patients with depression. The secondary objectives are to evaluate the safety of saredutant, to evaluate the efficacy of saredutant on disability and quality of life in patients with depression, and to evaluate blood levels of saredutant.
NCT00336713 ↗ A 24-52-week Study to Evaluate the Long-term Efficacy and Safety of Saredutant in Patients With Depression (MAGENTA) Completed Sanofi Phase 3 The purpose of the study is to evaluate the long-term efficacy and safety of Saredutant in patients with depression. The primary objective is to evaluate the efficacy and safety of Saredutant 100 mg once daily compared to placebo in the prevention of relapse of depressive symptoms in outpatients with major depressive disorder who achieved an initial response to 12 weeks of open-label treatment with Saredutant.
>Trial ID>Title>Status>Phase>Summary
Showing 1 to 6 of 6 entries

Clinical Trial Conditions for Saredutant

Condition Name

82110012345678Depressive DisorderGeneralized AnxietyAnxietyDepressive Disorder, Major[disabled in preview]
Condition Name
Intervention Trials
Depressive Disorder 8
Generalized Anxiety 2
Anxiety 1
Depressive Disorder, Major 1
[disabled in preview] 0
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Condition MeSH

1010330-101234567891011Depressive DisorderDepressionDiseaseDepressive Disorder, Major[disabled in preview]
Condition MeSH
Intervention Trials
Depressive Disorder 10
Depression 10
Disease 3
Depressive Disorder, Major 3
[disabled in preview] 0
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Clinical Trial Locations for Saredutant

Trials by Country

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Trials by Country
Location Trials
United States 10
Mexico 5
France 4
Canada 4
Sweden 3
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Trials by US State

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Trials by US State
Location Trials
New Jersey 9
Pennsylvania 1
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Clinical Trial Progress for Saredutant

Clinical Trial Phase

100.0%002468101214Phase 3[disabled in preview]
Clinical Trial Phase
Clinical Trial Phase Trials
Phase 3 13
[disabled in preview] 0
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Clinical Trial Status

100.0%002468101214Completed[disabled in preview]
Clinical Trial Status
Clinical Trial Phase Trials
Completed 13
[disabled in preview] 0
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Clinical Trial Sponsors for Saredutant

Sponsor Name

trials02468101214Sanofi[disabled in preview]
Sponsor Name
Sponsor Trials
Sanofi 13
[disabled in preview] 0
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Sponsor Type

100.0%002468101214Industry[disabled in preview]
Sponsor Type
Sponsor Trials
Industry 13
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