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Journal of the American Academy of Dermatology
Sous presse. Epreuves corrigées par l'auteur. Disponible en ligne depuis le lundi 17 février 2020
Doi : 10.1016/j.jaad.2020.01.019
Health care regulation, the Food and Drug Administration (FDA), and access to medicine : Our experience with dupilumab for children
 

Chang Ye Wang, MD a, , Rui Rui Chloe Zheng, JD b, Zachary A. Doerrer, BSc c, Anastasia O. Kurta, DO a, Jacob J. Shelley, SJD b, d, Elaine C. Siegfried, MD a
a Department of Dermatology, Saint Louis University, St Louis, Missouri 
b Faculty of Law, University of Western Ontario, London, Ontario, Canada 
c School of Medicine, Saint Louis University, St Louis, Missouri 
d School of Health Studies, University of Western Ontario, London, Ontario, Canada 

Correspondence to: Chang Ye Wang, MD, 1755 S Grand Blvd, St Louis, MO 63104.1755 S Grand BlvdSt LouisMO63104

Abbreviations used : FDA



 Authors Wang and Zheng contributed equally to this work.
 Funding sources: None.
 Conflicts of interest: Dr Siegfried, possibly related: principal investigator clinical trial, consulting fees, and honorarium for Regeneron; consulting fees and honorarium for Sanofi Genzyme; consulting fees for UCB and AbbVie. Unrelated: consulting fees and honorarium for Verrica; consulting fees and Data Safety Monitoring Committees for LEO Pharma and Novan; consulting fees for Pfizer and Pierre Fabre; principal investigator, clinical trial for Janssen; and principal investigator for Lilly. Authors Wang, Zheng, Doerrer, Kurta, and Shelley have no conflicts of interest to declare.
 IRB approval status: The primary data used in this article are obtained from studies approved by the SLU IRB.
 Reprints not available from the authors.


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