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Atomoxetine

Generic Name
Atomoxetine
Brand Names
Strattera
Drug Type
Small Molecule
Chemical Formula
C17H21NO
CAS Number
83015-26-3
Unique Ingredient Identifier
ASW034S0B8
Background

Atomoxetine is a selective norepinephrine (NE) reuptake inhibitor used for the treatment of attention deficit hyperactivity disorder (ADHD). Also known as the marketed product Strattera, atomoxetine is used with other treatment modalities (psychological, educational, cognitive behaviour therapy, etc) to improve developmentally inappropriate symptoms associated with ADHD including distractibility, short attention span, hyperactivity, emotional lability, and impulsivity. Although the underlying pathophysiology that causes ADHD remains unclear, evidence suggests that dysregulation in noradrenergic and dopaminergic pathways plays a critical role in suboptimal executive functioning within prefrontal regions of the brain, which are involved in attention and memory. Atomoxetine has been shown to specifically increase NA and DA within the prefrontal cortex, but not in the nucleus accumbens (NA) or striatum. This is beneficial in the treatment of ADHD as DA activation in the subcortical NA and striatum is associated with many stimulant-associated side effects and an increase in abuse potential, which is a limiting factor associated with the use of stimulant medications such as Methylphenidate, Dextroamphetamine, and Lisdexamfetamine. Use of non-stimulant medications such as atomoxetine is therefore thought to offer a clinical advantage over the use of traditional medications for the management of ADHD. More recently, positron emission tomography (PET) imaging studies in rhesus monkeys have shown that atomoxetine also binds to the serotonin transporter (SERT), and blocks the N-methyl-d-aspartate (NMDA) receptor, indicating a role for the glutamatergic system in the pathophysiology of ADHD.

Long-acting formulations of psychostimulants (such as Methylphenidate, Dextroamphetamine, and Lisdexamfetamine) are typically considered the most effective and first-line treatment for ADHD in adults and children as recommended by CADDRA (Canadian ADHD Resource Alliance). However, these stimulant medications are limited by dose-related side effects and concerns of abuse. Many contain a blackbox warning stating that CNS stimulants, including methylphenidate-containing products and amphetamines, have a high potential for abuse and dependence. In particular, increased dopamine in key areas caused by these stimulant medications is associated with their reinforcing and addictive properties, and even amplifies the potency and reinforcing effects of other drugs of abuse such as amphetamines, making ADHD sufferers more susceptible to their addictive effects. Concerns about abuse potential have spurred research into medications with fewer effects on DA and the use of non-stimulant ADHD medications including atomoxetine, Modafinil and Guanfacine. The non-stimulant norepinephrine/dopamine reuptake inhibitor Bupropion (commonly used for the treatment of depression and for smoking cessation) has also been shown to be effective in the treatment of ADHD.

Indication

Atomoxetine is indicated for the treatment of attention deficit hyperactivity disorder (ADHD) in children and adults.

Associated Conditions
Attention Deficit Hyperactivity Disorder (ADHD)

Treatment of Adult ADHD With Atomoxetine or Atomoxetine and Buspar

Phase 2
Completed
Conditions
Attention Deficit Disorder With Hyperactivity
First Posted Date
2005-09-15
Last Posted Date
2008-07-15
Lead Sponsor
Pfizer
Target Recruit Count
241
Registration Number
NCT00174226
Locations
🇺🇸

Pfizer Investigational Site, Woodstock, Vermont, United States

Atomoxetine for the Treatment of Cannabis Dependence

Phase 2
Completed
Conditions
Cannabis Dependence
Interventions
First Posted Date
2005-09-14
Last Posted Date
2017-01-11
Lead Sponsor
National Institute on Drug Abuse (NIDA)
Target Recruit Count
16
Registration Number
NCT00167297
Locations
🇺🇸

University of Pennsylvania Treatment Rersearch Center, Philadelphia, Pennsylvania, United States

Atomoxetine as an Adjunct to Novel Antipsychotic Medication in the Treatment of Cognitive Deficits of Schizophrenia

Not Applicable
Completed
Conditions
Schizophrenia
First Posted Date
2005-09-12
Last Posted Date
2019-08-19
Lead Sponsor
University of Maryland, Baltimore
Target Recruit Count
30
Registration Number
NCT00161031
Locations
🇺🇸

Veterans Affairs Maryland Health Care System, Baltimore, Maryland, United States

🇺🇸

Maryland Psychiatric Research Center, Catonsville, Maryland, United States

Atomoxetine for Treating Marijuana-Abusing Adolescents Who Have Attention Deficit Hyperactivity Disorder

Phase 2
Completed
Conditions
Marijuana Abuse
Attention Deficit Disorder With Hyperactivity
Interventions
Other: placebo
First Posted Date
2005-09-02
Last Posted Date
2019-04-23
Lead Sponsor
New York State Psychiatric Institute
Target Recruit Count
2
Registration Number
NCT00142961
Locations
🇺🇸

Phoenix House, New York, New York, United States

A Combination of Two Currently Approved Drugs to Enhance the Treatment of Schizophrenia

Phase 1
Completed
Conditions
Schizophrenia
First Posted Date
2004-08-18
Last Posted Date
2006-07-20
Lead Sponsor
Eli Lilly and Company
Registration Number
NCT00089869
Locations
🇺🇸

"For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at (1-877-285-4559) or speak with your personal physician., Chula Vista, California, United States

🇺🇸

For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY(1-877-285-4559) or speak with your personal physician., Irving, Texas, United States

🇺🇸

"For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at (1-877-285-4559) or speak with your personal physician.", San Antonio, Texas, United States

Atomoxetine to Treat Adolescents With Coexisting Alcohol and Other Substance Use Disorder and ADHD

Phase 2
Completed
Conditions
Substance Use Disorders
Attention Deficit Hyperactivity Disorder
First Posted Date
2002-01-17
Last Posted Date
2010-04-28
Lead Sponsor
University of Pittsburgh
Target Recruit Count
24
Registration Number
NCT00029614
Locations
🇺🇸

Western Psychiatric Institute and Clinic, Pittsburgh, Pennsylvania, United States

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