Duloxetine

Generic Name
Duloxetine
Brand Names
Cymbalta, Drizalma, Irenka, Yentreve, Duloxetine Zentiva, Duloxetine Mylan, Duloxetine Lilly
Drug Type
Small Molecule
Chemical Formula
C18H19NOS
CAS Number
116539-59-4
Unique Ingredient Identifier
O5TNM5N07U
Background

Duloxetine is a dual serotonin and norepinephrine reuptake inhibitor. It was originally discovered in 1993 and developed by Eli Lilly and Company as LY248686. Duloxetine first received approval from the FDA in August, 2004 as Cymbalta for the treatment of Major Depressive Disorder. It has since received approval for a variety of indications including the tre...

Indication

Indicated for:

1) Management of Major Depressive Disorder.

2) Management of Generalized Anxiety Disorder.

3) Management of diabetic peripheral neuropathy.

4) Management of fibromyalgia.

5) Management of chronic musculoskeletal pain.

6) Management of osteoarthritis of the knee in adults.

7) Management of chronic lower back pain in adults.
...

Associated Conditions
Chronic Lower Back Pain (CLBP), Chronic Musculoskeletal Pain, Diabetic Peripheral Neuropathic Pain (DPN), Fibromyalgia, Generalized Anxiety Disorder, Major Depressive Disorder (MDD), Osteoarthritis of the Knee, Stress Urinary Incontinence (SUI)
Associated Therapies
-

Study of Brain Response to Emotional Pictures Using a fMRI While on Duloxetine

Phase 4
Completed
Conditions
Interventions
First Posted Date
2007-09-20
Last Posted Date
2016-10-03
Lead Sponsor
Indiana University School of Medicine
Target Recruit Count
10
Registration Number
NCT00532480
Locations
🇺🇸

Indiana University Adult Psychiatric Clinic, Indianapolis, Indiana, United States

An Open Trial of Duloxetine on Comorbid Major Depression and Chronic Headache

First Posted Date
2007-09-19
Last Posted Date
2007-09-19
Lead Sponsor
Kraepelin Psiquiatria Clinica
Target Recruit Count
30
Registration Number
NCT00531895
Locations
🇧🇷

Hospital SOCOR, Belo Horizonte, MG, Brazil

Open-Label Study of Duloxetine in the Treatment of Children and Adolescents With Major Depressive Disorder

Phase 2
Completed
Conditions
Interventions
First Posted Date
2007-09-14
Last Posted Date
2011-10-24
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
72
Registration Number
NCT00529789
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., Bellevue, Washington, United States

Duloxetine for Perimenopausal Depression

Phase 4
Completed
Conditions
First Posted Date
2007-08-17
Last Posted Date
2012-07-09
Lead Sponsor
University of Arizona
Target Recruit Count
7
Registration Number
NCT00517985
Locations
🇺🇸

Women's Mental Health Program; University of Arizona; Department of Psychiatry, Tucson, Arizona, United States

Safety and Efficacy Study in Subjects With Diabetic Neuropathic Pain

First Posted Date
2007-07-27
Last Posted Date
2013-01-23
Lead Sponsor
AbbVie (prior sponsor, Abbott)
Target Recruit Count
280
Registration Number
NCT00507936
Locations
🇺🇸

Site Reference ID/Investigator# 6052, Anaheim, California, United States

🇺🇸

Site Reference ID/Investigator# 5276, Clearwater, Florida, United States

🇵🇷

Site Reference ID/Investigator# 8121, San Juan, Puerto Rico

and more 46 locations

Duloxetine Versus Duloxetine Plus Non-Drug Therapy for Depression

Phase 4
Completed
Conditions
First Posted Date
2007-06-29
Last Posted Date
2007-07-02
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
940
Registration Number
NCT00494377
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., Wien, Austria

Duloxetine Versus Placebo for Fibromyalgia

Phase 3
Completed
Conditions
First Posted Date
2007-06-21
Last Posted Date
2007-06-21
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
345
Registration Number
NCT00489073
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., Indianapolis, Indiana, United States

Duloxetine Versus Paroxetine for Major Depression

Phase 3
Completed
Conditions
First Posted Date
2007-06-21
Last Posted Date
2007-06-21
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
480
Registration Number
NCT00489775
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., Beijing, China

Urge Incontinence Bladder Overactivity Study

Phase 2
Completed
Conditions
First Posted Date
2007-05-21
Last Posted Date
2007-05-21
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
300
Registration Number
NCT00475696
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., North York, Ontario, Canada

Efficacy and Safety Stress Urinary Incontinence Study

Phase 3
Completed
Conditions
First Posted Date
2007-05-21
Last Posted Date
2007-05-21
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
120
Registration Number
NCT00475358
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., Tao-Yuan, Taiwan

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