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Strattera (atomoxetine)

Massachusetts General Hospital · FDA-approved active Small molecule

Atomoxetine selectively inhibits the reuptake of norepinephrine in the brain, increasing norepinephrine levels in key attention and executive function circuits.

Atomoxetine selectively inhibits the reuptake of norepinephrine in the brain, increasing norepinephrine levels in key attention and executive function circuits. Used for Attention-deficit/hyperactivity disorder (ADHD) in children and adults.

At a glance

Generic nameStrattera (atomoxetine)
Also known asStrattera
SponsorMassachusetts General Hospital
Drug classSelective norepinephrine reuptake inhibitor (NRI)
TargetNorepinephrine transporter (NET)
ModalitySmall molecule
Therapeutic areaPsychiatry/Neurology
PhaseFDA-approved

Mechanism of action

By blocking the norepinephrine transporter (NET), atomoxetine prevents the reabsorption of norepinephrine from the synaptic cleft, leading to increased norepinephrine availability in the prefrontal cortex and other brain regions involved in attention and impulse control. This mechanism differs from stimulant medications and makes it a non-stimulant option for ADHD treatment.

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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