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Atomoxetine

Alternative Names: atomoxetine, strattera
Latest Update: 2025-01-17
Latest Update Note: Clinical Trial Update

Product Description

Atomoxetine is used as part of a total treatment program to increase the ability to pay attention and decrease impulsiveness and hyperactivity in children and adults with ADHD. Atomoxetine is in a class of medications called selective norepinephrine reuptake inhibitors (Sourced from: https://medlineplus.gov/druginfo/meds/a603013.html)

Mechanisms of Action: NRI Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Approved

Approved Countries: Algeria | Argentina | Australia | Austria | Bangladesh | Belgium | Brazil | Bulgaria | Canada | Chile | Colombia | Croatia | Cyprus | Czech | Denmark | Dominican Republic | Ecuador | Egypt | Estonia | Finland | Germany | Greece | Hong Kong | Hungary | Iceland | India | Indonesia | Ireland | Israel | Italy | Japan | Jordan | Korea | Lebanon | Lithuania | Luxembourg | Malaysia | Malta | Mexico | Morocco | Netherlands | New Zealand | Norway | Pakistan | Peru | Philippines | Poland | Portugal | Romania | Russia | Saudi Arabia | Singapore | Slovakia | Slovenia | South Africa | Spain | Sri Lanka | Sweden | Switzerland | Taiwan | Thailand | Tunisia | Turkey | Ukraine | United Arab Emirates | United Kingdom | United States | Uruguay | Venezuela

Approved Indications: Attention Deficit Disorder with Hyperactivity

Known Adverse Events: Abdominal Pain | Dizziness | Pain Unspecified | Erectile Dysfunction | Constipation

Company: Eli Lilly
Company Location: INDIANAPOLIS IN 46285
Company CEO: David A. Ricks
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Atomoxetine

Countries in Clinic: Japan, United States

Active Clinical Trial Count: 4

Highest Development Phases

Phase 3: Sleep Apnea, Obstructive

Phase 2: Rett Syndrome|Tourette Syndrome

Phase 1: Attention Deficit Disorder with Hyperactivity

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

APC-APN-306

P3

Enrolling by invitation

Sleep Apnea, Obstructive

2026-06-30

ATO-TS

P2

Active, not recruiting

Tourette Syndrome|Rett Syndrome

2022-07-10

MARIPOSA

P2

Not yet recruiting

Sleep Apnea, Obstructive

2022-04-01

32%

JapicCTI-101245

P1

Active

Attention Deficit Disorder with Hyperactivity

None

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