Clinical Trial: Evaluating the Safety and Efficacy of Deucravacitinib Compared to Placebo Hidradenitis Suppurativa (HS).
Study Status: Completed
Recruit Status: RECRUITING
Condition: Hidradenitis Suppurativa
Study Type: INTERVENTIONAL
Official Title: A Pilot Study Evaluating the Safety and Efficacy of Deucravacitinib Compared to Placebo in the Treatment of Moderate-to-severe Hidradenitis Suppurativa (HS).
Brief Summary:
The study is a randomized, proof of concept study.30 patients aged 18 and over with HS will be included in this single center, randomized, double-blind, parallel-group study.Dosage of deucravacitinib will be given according to the investigational regimen as follows: 6 mg po bid for 16 weeks.The study compromises a 4-week screening period, a 16-week study period, and a 4-week follow-up period.The follow-up period consists of a follow-up phone call 4 weeks after the last study drug dose.
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