Trial for Hidradenitis Suppurativa (30 Weeks)

Males and females aged 18 years or older with moderate to severe hidradenitis suppurativa (HS) for at least 1 year, may qualify to participate. Individuals must have HS lesions present in at least 2 distinct areas of the body, with a total abscess and inflammatory nodule (AN) count of 5 or more, as well as a total draining fistula count of 20 or less. Looking for individuals who are biologic naïve or have failed previous TNF inhibitor treatments (e.g. adalimumab).

Participants will have a 2 to 1 chance of receiving investigational medication (active study drug) versus placebo, via 3 weekly intravenous infusions, followed by subcutaneous injections every 2 weeks thereafter. At End of Treatment, participants may roll-over into an open-label extension study if they qualify. Study medication and study-related procedures will be provided at no cost. Reimbursement for study-related expenses will also be provided.

Study participation will last about 30 weeks and involve about 11 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