Escitalopram

Generic Name
Escitalopram
Brand Names
Cipralex, Lexapro
Drug Type
Small Molecule
Chemical Formula
C20H21FN2O
CAS Number
128196-01-0
Unique Ingredient Identifier
4O4S742ANY
Background

Escitalopram is a selective serotonin re-uptake inhibitor (SSRI) and the S-enantiomer of racemic citalopram. It is used to restore serotonergic function in the treatment of depression and anxiety. Escitalopram is approximately 150 times more potent than citalopram’s R-enantiomer and is responsible for the vast majority of citalopram’s clinical activity, with...

Indication

Escitalopram is indicated for the acute and maintenance treatment of major depressive disorder (MDD) in adults and pediatric patients 12 years old and older and for the acute treatment of generalized anxiety disorder (GAD) in adults and pediatric patients 7 years old and older. It is additionally indicated for symptomatic relief of obsessive-compulsive disor...

Associated Conditions
Anxiety, Generalized Anxiety Disorder, Major Depressive Disorder (MDD), Obsessive Compulsive Disorder (OCD)
Associated Therapies
-

Acamprosate Added to Escitalopram and Behavioral Treatment for Comorbid Depression and Alcoholism

First Posted Date
2007-03-27
Last Posted Date
2012-07-09
Lead Sponsor
Massachusetts General Hospital
Target Recruit Count
23
Registration Number
NCT00452543
Locations
🇺🇸

Massachusetts General Hospital, Boston, Massachusetts, United States

Escitalopram and Sleep Architecture in Patients With Major Depressive Disorder

Phase 4
Conditions
First Posted Date
2007-03-02
Last Posted Date
2007-03-02
Lead Sponsor
Sheba Medical Center
Target Recruit Count
25
Registration Number
NCT00442481
Locations
🇮🇱

Sheba Medical Center, Department of psychiatry, Tel Hashomer, Israel

Discontinuation of Antipsychotics and Antidepressants Among Patients With BPSD

First Posted Date
2007-02-09
Last Posted Date
2007-08-24
Lead Sponsor
Sykehuset Innlandet HF
Target Recruit Count
24
Registration Number
NCT00433121
Locations
🇳🇴

Sykehuset Innlandet HF - Sanderud, Ottestad, Oppland, Norway

Efficacy and Safety of SR58611A co-Administered With Escitalopram in Adults With Major Depressive Disorder

First Posted Date
2007-02-08
Last Posted Date
2009-03-25
Lead Sponsor
Sanofi
Target Recruit Count
510
Registration Number
NCT00432614
Locations
🇹🇷

Sanofi-Aventis Administrative Office, Istanbul, Turkey

Galantamine Augmentation of Escitalopram for Treatment of Depression

Phase 4
Terminated
Conditions
First Posted Date
2007-01-18
Last Posted Date
2007-01-18
Lead Sponsor
Indiana University School of Medicine
Target Recruit Count
20
Registration Number
NCT00423969
Locations
🇺🇸

IU Adult Psychiatric Clinic, Indianapolis, Indiana, United States

A Study for Participants With Major Depression

First Posted Date
2007-01-09
Last Posted Date
2018-04-27
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
469
Registration Number
NCT00420004
Locations
🇷🇴

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Lasi, Romania

Escitalopram in Depressive Patients With Acute Coronary Artery Syndrome

First Posted Date
2007-01-08
Last Posted Date
2013-06-13
Lead Sponsor
Chonnam National University Hospital
Target Recruit Count
300
Registration Number
NCT00419471
Locations
🇰🇷

Chonnam National University Hospital, Gwangju, Korea, Republic of

An Eight-week Study to Evaluate the Efficacy and Safety of Saredutant in Patients With Generalized Anxiety Disorder

First Posted Date
2006-12-29
Last Posted Date
2016-05-24
Lead Sponsor
Sanofi
Target Recruit Count
365
Registration Number
NCT00417118
Locations
🇹🇷

Sanofi-Aventis Administrative Office, Istanbul, Turkey

An Eight-week Study Evaluating the Efficacy of a 100mg Dose of Saredutant Once Daily, in Elderly Patients With Major Depressive Disorder

First Posted Date
2006-12-22
Last Posted Date
2016-05-24
Lead Sponsor
Sanofi
Target Recruit Count
393
Registration Number
NCT00415142
Locations
🇹🇷

Sanofi-Aventis Administrative Office, Istanbul, Turkey

Evaluation of the Effects of Duloxetine on Norepinephrine

Phase 1
Completed
Conditions
First Posted Date
2006-12-21
Last Posted Date
2007-06-12
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
35
Registration Number
NCT00414323
Locations
🇺🇸

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., San Antonio, Texas, United States

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