Schlessinger, Joel
Shepard, Julie S.
Gower, Richard
Su, John C. http://orcid.org/0000-0002-4021-5423
Lynde, Charles
Cha, Amy
Ports, William C.
Purohit, Vivek
Takiya, Liza
Werth, John L.
Zang, Chuanbo
Vlahos, Bonnie
,
Clinical trials referenced in this document:
Documents that mention this clinical trial
Safety, Effectiveness, and Pharmacokinetics of Crisaborole in Infants Aged 3 to < 24 Months with Mild-to-Moderate Atopic Dermatitis: A Phase IV Open-Label Study (CrisADe CARE 1)
https://doi.org/10.1007/s40257-020-00510-6
Funding for this research was provided by:
Pfizer
Article History
First Online: 24 March 2020
Change Date: 17 September 2021
Change Type: Update
Change Details: A peer-reviewed video abstract, plain language summary, and digital features link was retrospectively added to this publication
Compliance with Ethical Standards
:
: <i>J. Schlessinger</i> has no conflicts of interest to declare. <i>J. S. Shepard</i> was compensated as a principal investigator for this study and was also compensated to serve on an advisory board for Pfizer Inc. <i>R. Gower</i> has received research grants for Pfizer crisaborole clinical trials, and consulting fees for participating in the Pfizer Crisaborole Advisory Board. <i>J. C. Su</i> has been an investigator, speaker, and/or advisor for Pfizer Inc., Amgen, AbbVie, Ego Pharmaceuticals, Eli Lilly, GlaxoSmithKline, Janssen/Johnson & Johnson, L’Oréal, Meda, Novartis, Pierre Fabre, and Sanofi. <i>C. Lynde</i> has served as a principal investigator, consultant, and/or speaker for Pfizer Inc., AbbVie, Bausch, Celgene, Eli Lilly, Janssen, LEO Pharma, Novartis, and Valeant. <i>A. Cha, V. Purohit, L. Takiya, J. L. Werth, C. Zang,</i> and <i>B. Vlahos</i> are employees and stockholders of Pfizer Inc. <i>W. C. Ports</i> was an employee of Pfizer Inc. at the time of this study and is a stockholder of Pfizer Inc.
: The institutional review board at each study site approved the study protocol, and written informed consent was provided by parents/legal guardians. The study was conducted in accordance with the protocol, local legal and regulatory requirements, and the general principles set forth in the International Ethical Guidelines for Biomedical Research Involving Human Subjects, International Conference on Harmonisation Guideline for Good Clinical Practice, and the Declaration of Helsinki.
: Written informed consent was provided by parents or legal guardians of participants of the study.