Study to Evaluate the Maximal Use of Ruxolitinib Cream in Adult and Adolescent Participants With Hidradenitis Suppurativa

Recruiting Phase 1 Interventional Study
Hidradenitis Suppurativa
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
12 – 75
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
24 (estimated)
Sponsor
Incyte Corporation · Industry
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About This Trial

The purpose of this study is to evaluate the maximal use of ruxolitinib cream in adult and adolescent participants with hidradenitis suppurativa.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Diagnosis of HS for at least 6 months before screening visit. * Diagnosis of HS (Hurley Stage I, II, III) with a total abscess and inflammatory nodule count of at least 4 and affecting at least 3 distinct anatomical areas at screening and Day 1 visits. * Total estimated treatm…
Contacts

Incyte Corporation Call Center (US)

1.855.463.3463

medinfo@incyte.com

CONTACT

Incyte Corporation Call Center (ex-US)

+800 00027423

eumedinfo@incyte.com

CONTACT