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Dr Anisa Rowhani-Farid, Department of Practice, Sciences, and Health Outcomes Research, University of Maryland Baltimore, Baltimore, MD 21201, USA. Email: anisarowhani@gmail.com
AR-F designed and led the study, extracted and verified data, conducted the statistical analyses, wrote the first draft of the manuscript, edited the manuscript and is the guarantor of the study; KH extracted and verified data and edited the manuscript; MG extracted and verified data and edited the manuscript; JR provided statistical consulting for the study and edited the manuscript; ADZ verified data and edited the manuscript; JDW provided statistical consulting and edited the manuscript and JSR designed the study, provided statistical consulting, edited the manuscript and provided mentorship for AR-F’s postdoctoral fellowship throughout the study.
When this work was conducted, the salaries of AR-F and KH were supported by the RIAT Support Center at the University of Maryland. The RIAT Support Center was supported by the Laura and John Arnold Foundation. KH was supported by the Food and Drug Administration (FDA) of the US Department of Health and Human Services (HHS) as part of a financial assistance award U01FD005946, unrelated to this manuscript, totalling US$5000 with 100% funded by FDA/HHS. The statistical support for this publication, provided by JR, was made possible by CTSA Grant Number UL1 TR001863 from the National Center for Advancing Translational Science (NCATS), a component of the National Institutes of Health (NIH). ADZ currently receives research support from the National Institutes of Aging through the Duke Creating ADRD Researchers for the Next Generation—Stimulating Access to Research in Residency (CARiNG-StARR) programme (R38AG065762). JDW reported receiving grant support by the US Food and Drug Administration, Arnold Ventures, Johnson & Johnson through Yale University, and the National Institute on Alcohol Abuse and Alcoholism of the National Institutes of Health under award No. 1K01AA028258; he reported serving as a consultant for Hagens Berman Sobol Shapiro LLP and Dugan Law Firm APLC. JSR currently receives research support through Yale University from Johnson and Johnson to develop methods of clinical trial data sharing, from the Medical Device Innovation Consortium as part of the National Evaluation System for Health Technology (NEST), from the Food and Drug Administration for the Yale-Mayo Clinic Center for Excellence in Regulatory Science and Innovation (CERSI) programme (U01FD005938), from the Agency for Healthcare Research and Quality (R01HS022882), from the National Heart, Lung and Blood Institute of the National Institutes of Health (NIH) (R01HS025164, R01HL144644) and from the Laura and John Arnold Foundation to establish the Good Pharma Scorecard at Bioethics International; in addition, JSR is an expert witness at the request of Relator’s attorneys, the Greene Law Firm, in a qui tam suit alleging violations of the False Claims Act and Anti-Kickback Statute against Biogen. MG has no conflicts of interest to disclose.
The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.