Systemic timolol exposure following topical application to infantile hemangiomas - 11/02/20
Doi : 10.1016/j.jaad.2019.02.029
Beth A. Drolet, MD a, ⁎ 
, Felix Boakye-Agyeman, MD b, Barrie Harper, BSMT (ASCP), PMP b, Kristen Holland, MD a, Andrew Lewandowski, PhD c, Nicole Stefanko, MD a, Chiara Melloni, MD, MHS b
on behalf of the
, Felix Boakye-Agyeman, MD b, Barrie Harper, BSMT (ASCP), PMP b, Kristen Holland, MD a, Andrew Lewandowski, PhD c, Nicole Stefanko, MD a, Chiara Melloni, MD, MHS bon behalf of the
Pediatric Trials Network Steering Committee (See Acknowledgments for a listing of committee members.)
Gary Furda, Danny Benjamin, Edmund Capparelli, Gregory L. Kearns, Ian M. Paul, Christoph Hornik, Kelly Wade
a Medical College of Wisconsin, Milwaukee, Wisconsin
b Duke Clinical Research Institute, Duke University Medical Center, Durham, North Carolina
c The Emmes Corporation, Rockville, Maryland
∗Correspondence to: Beth A. Drolet, MD, University of Wisconsin, The School of Medicine and Public Health.University of WisconsinThe School of Medicine and Public Health
| Funding sources: Supported under National Institute of Child Health and Human Development contract HHSN275201000003I for the Pediatric Trials Network (principal investigator, Danny Benjamin). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. |
|
| Disclosure: Dr Drolet reports an investigator-initiated trial examining the safety of oral propranolol for treatment of infantile hemangioma that was sponsored by Pierre Fabre. She is owner and co-founder of Peds Derm Development Group, LLC. Dr Boakye-Agyeman, Mr Harper, Dr Holland, Dr Lewandowski, and Dr Stefanko have no conflicts of interest to disclose. |
© 2019
American Academy of Dermatology, Inc.. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 82 - N° 3
P. 733-736 - mars 2020 Retour au numéro
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