A phase 2a trial of brepocitinib for cicatricial alopecia

Brepocitinib significantly reduces CCL5 expression and was well tolerated at week 24, meeting coprimary endpoints. Brepocitinib reduces inflammatory biomarker expression and improves clinical severity, while maintaining favorable safety profile.

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Publication Details

Journal
Journal of the American Academy of Dermatology
Published
2024-10-25
DOI
https://doi.org/10.1016/j.jaad.2024.09.073
Citations
18
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
Field-Weighted Citation Impact
7.65

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article

A phase 2a trial of brepocitinib for cicatricial alopecia

Ester Del Duca, Ping Mahling, Emma Guttman‐Yassky, Swaroop Bose et al.
18 citations
Journal of the American Academy of Dermatology
Autoimmune Bullous Skin Diseases
7.65
article

A phase 2a trial of brepocitinib for cicatricial alopecia

Ester Del Duca, Ping Mahling, Emma Guttman‐Yassky, Swaroop Bose, Kelly Hawkins, Barry S. Oemar, Eden David, Yeriel Estrada, Benjamin Ungar, Elena Peeva, Juliana Pulsinelli, Celina Dubin, Neda Shokrian, Joel Corrêa da Rosa, Marguerite Meariman, Elizabeth Andrews, Giselle Singer, Savina Sikand
article en
18 citations

Abstract

Brepocitinib significantly reduces CCL5 expression and was well tolerated at week 24, meeting coprimary endpoints. Brepocitinib reduces inflammatory biomarker expression and improves clinical severity, while maintaining favorable safety profile.

Journal of the American Academy of DermatologyVol. 92(3)
University of Rome Tor Vergata (IT), Albert Einstein College of Medicine (US), Pfizer (United States) (US), Icahn School of Medicine at Mount Sinai (US)
Eli Lilly and Company, Pfizer, GlaxoSmithKline, Sanofi, Celgene, Regeneron Pharmaceuticals, Dermira, Incyte, Castle Biosciences, Glenmark Pharmaceuticals, Galderma, LEO Pharma
Zero hunger
Openalex Percentile: Top 2%
Autoimmune Bullous Skin Diseases
7.65
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