CLINICAL TRIALS PROFILE FOR SAREDUTANT

Clinical Trials for Saredutant

Trial ID	Title	Status	Sponsor	Phase	Summary
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.

Clinical Trial Conditions for Saredutant

Condition Name

Condition Name for
Intervention	Trials
Depressive Disorder	8
Generalized Anxiety	2
Depressive Disorder, Major	1
Major Depressive Disorder	1

Condition MeSH

Condition MeSH for
Intervention	Trials
Depressive Disorder	10
Depression	10
Disease	3
Depressive Disorder, Major	3

Clinical Trial Locations for Saredutant

Trials by Country

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

Trials by US State

Trials by US State for
Location	Trials
New Jersey	9
Pennsylvania	1

Clinical Trial Progress for Saredutant

Clinical Trial Phase

Clinical Trial Phase for
Clinical Trial Phase	Trials
Phase 3	13

Clinical Trial Status

Clinical Trial Status for
Clinical Trial Phase	Trials
Completed	13

Clinical Trial Sponsors for Saredutant

Sponsor Name

Sponsor Name for
Sponsor	Trials
Sanofi	13

Sponsor Type

Sponsor Type for
Sponsor	Trials
Industry	13