Research Trial for Hidradenitis Suppurativa (51 Weeks)

Male or female patients from 18 to 65 years of age with a diagnosis of hidradenitis suppurativa (HS) for at least 6 months, may be eligible to participate. Note: individuals with a clinical history of HS may also be considered for enrollment. HS lesions must be present in at least 2 distinct anatomical regions. As well, individuals must have had an inadequate response or intolerance to a 28-day course of oral antibiotics. A total abscess and inflammatory nodule count of 4 or greater, is also required.

Participants will receive investigational medication (active study drug) or placebo, via IV infusion. Study medication and study-related care will be provided at no cost. Reimbursement for study-related expenses will also be provided. An over-the-counter topical antiseptic must be used daily throughout the duration of the study, on body areas affected with HS lesions.

Study participation will last about 51 weeks and involve about 20 visits to the study centre.

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Hidradenitis Suppurativa
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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