Landersdorfer, Cornelia B.
Findling, Robert L.
Frazier, Jean A.
Kafantaris, Vivian
Kirkpatrick, Carl M. J.
Funding for this research was provided by:
National Institute of Child Health and Human Development (HHSN275200503406C)
National Institute of Child Health and Human Development
National Health and Medical Research Council (APP1062509)
Article History
First Online: 8 July 2016
Compliance with Ethical Standards
:
: This work was supported by the Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services (Contract No. HHSN275200503406C) and the Australian National Health and Medical Research Council (Career Development Fellowship number 1062509 to CBL).
: Dr. Findling receives or has received research support, acted as a consultant and/or served on a Speaker’s Bureau for Alcobra, American Academy of Child and Adolescent Psychiatry, American Physician Institute, American Psychiatric Press, AstraZeneca, Bracket, Bristol-Myers Squibb, CogCubed, Cognition Group, Coronado Biosciences, Dana Foundation, Elsevier, Forest, GlaxoSmithKline, Guilford Press, Johns Hopkins University Press, Johnson and Johnson, Jubilant Clinsys, KemPharm, Lilly, Lundbeck, Merck, NIH, Neurim, Novartis, Noven, Otsuka, Oxford University Press, Pfizer, Physicians Postgraduate Press, Purdue, Rhodes Pharmaceuticals, Roche, Sage, Shire, Sunovion, Supernus Pharmaceuticals, Transcept Pharmaceuticals, Validus and WebMD. Dr. Kirkpatrick has undertaken collaborative research projects unrelated to the current work with Roche and d3 Medicine. Dr. Kafantaris has received research support from AstraZeneca, the Brain and Behavior Foundation, Bristol-Myers Squibb, Forest Pharmaceuticals, GlaxoSmithKline, Janssen, Eli Lilly, Merck, Pfizer and Sunovion. Dr. Frazier has received research support from Alcobra, Janssen, Neuren, Roche and SyneuRX International and has served on a data safety monitoring board for Forest Pharmaceuticals.
: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
: Written assent was obtained from all participants included in the study and written informed consent was given by each participant’s guardian.