Weiss, Margaret Danielle http://orcid.org/0000-0001-8153-8213
Surman, Craig
Khullar, Atul
He, Ellie
Cataldo, Marc
Donnelly, Graeme
Funding for this research was provided by:
Purdue Pharma L.P.
Article History
Accepted: 26 March 2021
First Online: 31 May 2021
Declarations
:
: This analysis was funded by Purdue Pharma L.P., who also paid the open access fee.
: MW has received consulting fees/honoraria from Tris, Purdue, Adlon, Takeda, Huron, Mundipharma, and CBPartners; support for travel to meetings, manuscript preparation, or other purposes from World Federation of ADHD, Eunethydis, Canadian Attention Deficit Disorder Resource Alliance (CADDRA), Children and Adults with Attention Deficit Disorder (CHADD), American Professional Society for ADHD and Related Disorders (APSARD), Israeli Federation of ADHD, Purdue CA, Purdue US, Rhodes Pharmaceutical, Akili, Takeda, Global Medical Education, and Boston Children’s Hospital; payment for lectures from Global Medical Education, Centre for ADHD Awareness Canada (CADDAC), and CADDRA; and royalties from Multi Health Systems and Johns Hopkins University Press. CS has received consulting fees from Eisai, McNeil, NLS Pharma, Nutricia, Pfizer, Adlon/Purdue, Rhodes, Shire, Somaxon, Sunovion, Takeda, and Teva; payment for lectures from Alcobra, Arbor, Janssen, Janssen-Ortho, McNeil, Novartis, Shire, Reed/MGH Academy (multiple companies), and GME CME (multiple companies); research funding from Abbot, Cephalon, Hilda and Preston Davis Foundation, Eli Lilly, Magceutics/Neurocentria, Johnson & Johnson/McNeil, Lundbeck, Merck, Nordic Naturals, Shire, and Takeda; and royalties from Berkeley/Penguin (for <i>FAST MINDS. How to Thrive if You Have ADHD (or Think You Might)</i>) and Humana/Springer (for <i>ADHD in Adults: A Practical Guide to Evaluation and Management</i>). AK has received consulting fees/honoraria and payment for lectures from Elysium and Purdue. EH is a full-time employee of Imbrium Therapeutics, a subsidiary of Purdue Pharma L.P., the sponsor of this study. MC is a full-time employee of Purdue Pharma L.P., the sponsor of this study. GD is an employee of Purdue Pharma (Canada).
: The studies were conducted in Canada and the USA in 2014–2015 in accordance with the Declaration of Helsinki, good clinical practice, and national and local laws. They were approved by a central institutional review board (IRB Services, Aurora, ON, Canada; now known as Advarra) or, if required, by a local institutional review board.
: All participants provided written informed consent before any study-related procedures.
: Not applicable.
: The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
: Not applicable.
: MW, MC, and GD were responsible for the conception or design of the work. GD and EH were responsible for data collection. MW, MC, and GD drafted the article. All authors were responsible for data analysis and interpretation, critical revision of the article, and final approval of the version to be published and agree to be accountable for all aspects of the work.