MedPath

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)

Bariatric Surgery and Pharmacokinetics of Atomoxetine

Completed
Conditions
Obesity, Morbid
First Posted Date
2018-03-09
Last Posted Date
2024-10-07
Lead Sponsor
Norwegian University of Science and Technology
Target Recruit Count
12
Registration Number
NCT03460210
Locations
🇳🇴

St. Olavs University Hospital, Trondheim, Norway

Efficacy and Safety of Midodrine and Atomoxetine for Neurogenic OH

Phase 4
Completed
Conditions
Neurogenic Orthostatic Hypotension
Interventions
First Posted Date
2017-11-22
Last Posted Date
2019-04-05
Lead Sponsor
Seoul National University Hospital
Target Recruit Count
50
Registration Number
NCT03350659
Locations
🇰🇷

Seoul National University Hospital, Seoul, Korea, Republic of

The Safety and Efficacy of OPC-64005 in the Treatment of Adult Attention-deficit/Hyperactivity Disorder

Phase 2
Completed
Conditions
Adult Attention Deficit Hyperactivity Disorder
Interventions
First Posted Date
2017-10-27
Last Posted Date
2021-10-29
Lead Sponsor
Otsuka Pharmaceutical Development & Commercialization, Inc.
Target Recruit Count
239
Registration Number
NCT03324581
Locations
🇺🇸

iResearch Atlanta, Decatur, Georgia, United States

🇺🇸

Premier Psychiatric Research Institute, LLC, Lincoln, Nebraska, United States

🇺🇸

Psychiatric Associates, Overland Park, Kansas, United States

and more 21 locations

Atomoxetine PBPK-PD Clinical Study

Completed
Conditions
ADHD
First Posted Date
2017-05-16
Last Posted Date
2023-08-08
Lead Sponsor
Children's Mercy Hospital Kansas City
Target Recruit Count
51
Registration Number
NCT03154359
Locations
🇺🇸

Children's Mercy Hospital and Clinics, Kansas City, Missouri, United States

Recall Enhancement Through Treatment With Atomoxetine in MS (RETAIN-MS)

Phase 2
Completed
Conditions
Memory Disorders
Multiple Sclerosis
Interventions
Drug: Placebo
First Posted Date
2017-03-27
Last Posted Date
2020-03-13
Lead Sponsor
Icahn School of Medicine at Mount Sinai
Target Recruit Count
11
Registration Number
NCT03091400
Locations
🇺🇸

Icahn School of Medicine at Mount Sinai, New York, New York, United States

TAME-PD - Physical Therapy, Atomoxetine And, Methylphenidate, to Enhance Gait and Balance in Parkinson's Disease

Early Phase 1
Recruiting
Conditions
Parkinson's Disease, Idiopathic
Interventions
First Posted Date
2016-08-25
Last Posted Date
2025-01-17
Lead Sponsor
Hubert Fernandez
Target Recruit Count
42
Registration Number
NCT02879136
Locations
🇺🇸

Cleveland Clinic, Cleveland, Ohio, United States

Post-stroke Neural Plasticity With Atomoxetine

Phase 2
Completed
Conditions
Atomoxetine Hydrochloride
Placebos
Interventions
Drug: Placebo
First Posted Date
2016-06-02
Last Posted Date
2017-08-14
Lead Sponsor
Lumy Sawaki
Target Recruit Count
12
Registration Number
NCT02788357

Norepinephrine Transporter Blockade, Autonomic Failure (NETAF)

Phase 2
Completed
Conditions
Neurogenic Orthostatic Hypotension
Interventions
Drug: Placebo
First Posted Date
2016-05-27
Last Posted Date
2023-09-13
Lead Sponsor
Vanderbilt University Medical Center
Target Recruit Count
48
Registration Number
NCT02784535
Locations
🇺🇸

Dysautonomic Center at NYU Langone Medical Center, New York, New York, United States

🇺🇸

Vanderbilt University Medical Center, Nashville, Tennessee, United States

Attention-deficit/Hyperactivity Disorder Translational Center for Identifying Biomarkers

Phase 4
Conditions
Attention-deficit/Hyperactivity Disorder
Interventions
First Posted Date
2015-12-07
Last Posted Date
2015-12-07
Lead Sponsor
Seoul National University Childrens Hospital
Target Recruit Count
400
Registration Number
NCT02623114
Locations
🇰🇷

Seoul National University Children's Hospital, Seoul, Korea, Republic of

Prevention of Syncope Trial 6 - Atomoxetine in Vasovagal Syncope

Phase 2
Completed
Conditions
Vasovagal Syncope
Interventions
Drug: Placebo
First Posted Date
2015-07-16
Last Posted Date
2020-04-21
Lead Sponsor
University of Calgary
Target Recruit Count
57
Registration Number
NCT02500732
Locations
🇨🇦

University of Calgary, Calgary, Alberta, Canada

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