Long-term Safety of Ketoconazole Foam, 2% in the Treatment of Seborrheic Dermatitis: Results of a Phase IV, Open-Label Study

January 2013 | Volume 12 | Issue 1 | Original Article | 1 | Copyright © January 2013


Zoe D. Draelos MD a, Steven R. Feldman MD PhD b, Victoria Butners BSc c, and Alessandra B. Alió Saenz MD c

aDepartment of Dermatology, Duke University School of Medicine, Durham, NC bDepartment of Dermatology, Wake Forest University, Winston-Salem, NC cStiefel, a GlaxoSmithKline (GSK) company, Research Triangle Park, NC

table 5
ing principal investigators: Texas: W. Abramovits, M. Jarratt, A. Menter, A. Moore, A. Pandya; California: E. Boh; North Carolina: Z. Draelos, S. Feldman; Alabama: B. Elewski; Rhode Island: E. Frankel; Massachusetts: A. Kimball; Virginia: D. Pariser; Florida: M. Rendon, D. Rodriguez, J. Spencer, S. Weiss; Oregon: P. Rich; Michigan: L. Stein Gold. The authors thank Alyson Bexfield PhD of Caudex Medical, Oxford, UK (supported by Stiefel, a GSK company, Research Triangle Park, NC), for assistance with preparing the initial draft of the manuscript, collating the authors’ comments, and assembling the tables.

DISCLOSURES

Dr. Draelos has received research support from Stiefel, a GSK company, including in relation to the study presented here. Dr. Feldman has received speaking, research, and/or consulting support from Stiefel/GSK, Astellas, Novartis, and Galderma Laboratories. Ms. Butners and Dr. Alió Saenz are employees of Stiefel, a GSK company.
This study was supported by Stiefel, a GSK company, Research Triangle Park, NC.

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AUTHOR CORRESPONDENCE

Zoe D. Draelos MDzdraelos@northstate.net