Journal of the American Academy of Child & Adolescent Psychiatry
Volume 48, Issue 5 , Pages 511-518, May 2009

Clinical Responses to Atomoxetine in Attention-Deficit/Hyperactivity Disorder: The Integrated Data Exploratory Analysis (IDEA) Study

Dr. Newcorn is with the Department of Psychiatry, Mount Sinai School of Medicine; Dr. Weiss is with the Division of Child Psychiatry, University of British Columbia. Dr. Sutton is with i3 Research; Dr. Sumner is with Bio-behavioral Diagnostics Company

Accepted 8 January 2009.

Disclosure: Dr. Newcorn has received grants for research support from Eli Lilly and Ortho-McNeil-Janssen. He has been a consultant and/or advisor to Abbott, BioBehavioral Diagnostics, Eli Lilly, Novartis, Ortho-McNeil-Janssen, Psychogenics, Sanofi-Aventis, and Shire, and a speaker for Ortho-McNeil-Janssen. Dr. Weiss has consulting, speaking, honoraria, and research funding from Eli Lilly, Shire, Janssen, and Purdue, as well as a consulting agreement with Takeda. Drs. Sutton and Sumner were with Lilly Research Laboratories, Eli Lilly & Company, when the study was performed.

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 Funding for this research was provided by Eli Lilly and Company.The authors thank Stephen W. Gutkin of Rete Biomedical Communications for assistance in manuscript preparation.Clinical trials registration information—Evaluation of Continuous Symptom Treatment of ADHD: A Placebo-Controlled Double-Blind Assessment of Morning-Dosed or Evening-Dosed Strattera. URL: http://www.clinicaltrials.gov. Unique identifier: NCT00486122. Results of the other studies analyzed in the Integrated Data Exploratory Analysis study are posted at www.clinicalstudyresults.org, ID numbers 5670, 7972, 2746, 1585, 1586, and 3468, and www.lillytrials.com.

PII: S0890-8567(09)60068-X

doi:10.1097/CHI.0b013e31819c55b2

Journal of the American Academy of Child & Adolescent Psychiatry
Volume 48, Issue 5 , Pages 511-518, May 2009

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