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Atomoxetine (ATO)

Janssen Research & Development, LLC · FDA-approved active Small molecule

Atomoxetine selectively inhibits the reuptake of norepinephrine in the central nervous system, increasing norepinephrine availability at synapses.

Atomoxetine selectively inhibits the reuptake of norepinephrine in the central nervous system, increasing norepinephrine availability at synapses. Used for Attention-deficit/hyperactivity disorder (ADHD) in children, adolescents, and adults, ADHD-related symptoms in patients with comorbid conditions.

At a glance

Generic nameAtomoxetine (ATO)
SponsorJanssen Research & Development, LLC
Drug classNorepinephrine reuptake inhibitor (NRI)
TargetNorepinephrine transporter (NET)
ModalitySmall molecule
Therapeutic areaPsychiatry / Neurology
PhaseFDA-approved

Mechanism of action

Atomoxetine is a selective norepinephrine reuptake inhibitor (NRI) that blocks the norepinephrine transporter, preventing the reabsorption of norepinephrine from the synaptic cleft. This increases norepinephrine concentration in key brain regions involved in attention and executive function. Unlike stimulant medications, it does not directly release norepinephrine or dopamine and has minimal abuse potential.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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