Research Study for Hidradenitis Suppurativa (85 Weeks)

Adults 18+ years of age with moderate to severe hidradenitis suppurativa (HS) for at least 1 year, may qualify to participate. Individuals must have at least 5 inflammatory nodules or abscesses, HS lesions present in at least 2 different areas of the body, and a draining fistula count of 20 or less at the time of study entry. Individuals must also have a history of inadequate response or intolerance to an adequate trial of oral antibiotics for the treatment of HS.

During Period A, participants will receive investigational medication (active study drug) or placebo, via injection. At Week 16, participants who previously received placebo will then receive active study drug and vice versa. At Week 20, all particpants will receive active study drug. Individuals will be required to use a daily antiseptic wash on their HS lesions, during the course of the study.

Study medication and study-related care will be provided at no cost. Reimbursement for study-related expenses may be provided.

Participation will last up to 85 weeks and involve about 17 visits to the study centre.

Call the study centre near you, or register now.

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Hidradenitis Suppurativa
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Participating Locations


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All information about you will be kept confidential.

If there are no active studies for your condition, we will keep your information and contact you when a new study starts in your area.

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Why Take Part In a Clinical Study?

Regulatory agencies like Health Canada, Australia's Therapeutic Goods Administration and the FDA require that Clinical Research Trials be conducted in order to develop new treatments, preventions and devices for diseases or conditions. Clinical Research Trials are also referred to as Clinical Studies or Clinical Trials. read more