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Reply to: "Lack of a US Food and Drug Administration indication should not limit access to appropriate treatment".

Savage KT, Flood KS, Popatia S, et al. Reply to: "Lack of a US Food and Drug Administration indication should not limit access to appropriate treatment".. Journal of the American Academy of Dermatology. 2019;81(1):e19-e20.

Publisher's Version

Last updated on 07/10/2024
PubMed

Recent Publications

Hidradenitis suppurativa: new insights into disease mechanisms and an evolving treatment landscape.
Efficacy and safety of the oral Janus kinase 1 inhibitor povorcitinib (INCB054707) in patients with hidradenitis suppurativa in a phase 2, randomized, double-blind, dose-ranging, placebo-controlled study.
Safety and efficacy of bimekizumab through 2 years in patients with moderate-to-severe plaque psoriasis: longer-term results from the BE SURE randomized controlled trial and the open-label extension from the BE BRIGHT trial.
Real-World Findings on the Characteristics and Treatment Exposures of Patients with Hidradenitis Suppurativa from US Claims Data.
Secukinumab in moderate-to-severe hidradenitis suppurativa (SUNSHINE and SUNRISE): week 16 and week 52 results of two identical, multicentre, randomised, placebo-controlled, double-blind phase 3 trials.
Efficacy and Safety of Risankizumab for the Treatment of Hidradenitis Suppurativa: A Phase 2, Randomized, Placebo-Controlled Trial.

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