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Last Updated: October 16, 2019

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CLINICAL TRIALS PROFILE FOR STRATTERA

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Clinical Trials for Strattera

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00174226 Treatment of Adult ADHD With Atomoxetine or Atomoxetine and Buspar Completed Pfizer Phase 2 2004-11-01 Determine if there is a difference in treatment response for adults with ADHD who are treated with Strattera versus those treated with a combination of Strattera and buspirone
NCT00181766 Strattera Treatment in Adults With Attention Deficit Hyperactivity Disorder Not Otherwise Specified (ADHD NOS) Completed Eli Lilly and Company Phase 4 2003-12-01 This is an open-label study with daily doses up to 144 mg/day Strattera (atomoxetine) in the treatment of adults with attention deficit hyperactivity disorder not otherwise specified. The researchers hypothesize ADHD symptomatology in adults with ADHD NOS will be responsive to Strattera treatment and Strattera treatment (in doses of up to 120 mg/day or 1.5 mg/kg/day, whichever is less) in adults with ADHD NOS will be safe and well tolerated.
NCT00181766 Strattera Treatment in Adults With Attention Deficit Hyperactivity Disorder Not Otherwise Specified (ADHD NOS) Completed Massachusetts General Hospital Phase 4 2003-12-01 This is an open-label study with daily doses up to 144 mg/day Strattera (atomoxetine) in the treatment of adults with attention deficit hyperactivity disorder not otherwise specified. The researchers hypothesize ADHD symptomatology in adults with ADHD NOS will be responsive to Strattera treatment and Strattera treatment (in doses of up to 120 mg/day or 1.5 mg/kg/day, whichever is less) in adults with ADHD NOS will be safe and well tolerated.
NCT00181948 Strattera Treatment in Children With ADHD Who Have Poor Response to Stimulant Therapy Completed Eli Lilly and Company Phase 4 2004-09-01 This will be a 6-week, unblinded study using the medication Strattera for children and adolescents with attention deficit hyperactivity disorder (ADHD) who failed to respond to an adequate trial of stimulant treatment. Specific hypotheses are as follows: Hypothesis 1: ADHD symptomatology in youth with ADHD will be responsive to Strattera treatment in the short term. Hypothesis 2: Strattera treatment (in doses of up to 120 mg/day or 1.2 mg/kg/day) in children and adolescents with ADHD will be safe and well tolerated.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Strattera

Condition Name

Condition Name for Strattera
Intervention Trials
Attention Deficit Hyperactivity Disorder 10
Attention Deficit Hyperactivity Disorder (ADHD) 4
ADHD 3
Attention Deficit Disorder With Hyperactivity 3
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Condition MeSH

Condition MeSH for Strattera
Intervention Trials
Attention Deficit Disorder with Hyperactivity 22
Hyperkinesis 14
Disease 9
Cocaine-Related Disorders 3
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Clinical Trial Locations for Strattera

Trials by Country

Trials by Country for Strattera
Location Trials
United States 39
Canada 2
Sweden 2
Spain 2
Italy 1
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Trials by US State

Trials by US State for Strattera
Location Trials
New York 5
Massachusetts 4
Maryland 3
Tennessee 3
Colorado 3
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Clinical Trial Progress for Strattera

Clinical Trial Phase

Clinical Trial Phase for Strattera
Clinical Trial Phase Trials
Phase 4 13
Phase 3 2
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for Strattera
Clinical Trial Phase Trials
Completed 23
Recruiting 4
Active, not recruiting 3
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Clinical Trial Sponsors for Strattera

Sponsor Name

Sponsor Name for Strattera
Sponsor Trials
Eli Lilly and Company 10
National Institute on Drug Abuse (NIDA) 5
Massachusetts General Hospital 3
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Sponsor Type

Sponsor Type for Strattera
Sponsor Trials
Other 37
Industry 15
NIH 11
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