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An Open-Label Study of Atomoxetine in Adolescents With Attention-Deficit/Hyperactivity Disorder

Phase 3
Completed
Conditions
Attention Deficit Hyperactivity Disorder
Registration Number
NCT00191737
Lead Sponsor
Eli Lilly and Company
Brief Summary

A single arm, open-label, phase 3 multicenter study to evaluate the effectiveness and tolerability of atomoxetine (given once daily, target dose 1.2 mg/kg/day), as perceived by patients, parents and physicians, and its impact on self-esteem in adolescents (aged 12 through 17 years) with Attention-Deficit/Hyperactivity Disorder treated as outpatients in Germany. An 8-week treatment phase is followed by a 16-week extension period.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
147
Inclusion Criteria
  • Male or female outpatients who are at least 12 years of age and who will not have reached their 18th birthday
  • Diagnosis of ADHD
  • Normal intelligence
Exclusion Criteria
  • Weigh less than 30 kg or more than 85 kg at study entry
  • Other relevant psychiatric diagnoses
  • Are at serious suicidal risk as determined by the investigator
  • Have a history of severe allergies
  • Alcohol or drug abuse within the past 3 months
  • Are female patients who are pregnant or breast-feeding. Sexually active females must use a medically acceptable method of contraception.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Global Impression of Perceived Difficulties (GIPD) scale at baseline, Week 8 and Week 24
Secondary Outcome Measures
NameTimeMethod
Pediatric Adverse Events Rating Scale (PAERS) during 8 and 24 weeks of treatment
Rosenberg Self-Esteem Scale (SES) during 8 and 24 weeks of treatment

Trial Locations

Locations (1)

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

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Koln, Germany

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