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COMPASS 2-HS – Adult’s Hidradenitis Suppurativa Study (40 Weeks)

For condition: Hidradenitis Suppurativa
Enrolling:
CL-BFB759-003

COMPASS 2-HS – Adult’s Hidradenitis Suppurativa Study (40 Weeks)

Study Summary

Who Can Participate?
Males or females aged ≥18 to ≤75 years with moderate to severe hidradenitis suppurativa (HS) may participate.

Inclusion Criteria
• have a diagnosis of HS based on clinical history and physical examination for at least ≥1 year
• have HS lesions present in at least 2 distinct anatomic areas
• have HS defined as a total of ≥5 inflammatory lesions (ie, number of abscesses plus number of inflammatory nodules)
• have either had an inadequate response, had intolerance, or had recurrence after ≥3 months systemic antibiotic for treatment of HS

Participant Information
• Participate and receive study treatment at no cost
• Regular visits with study doctors who specialise in treating HS (up to 22 visits)
• Will receive an investigative subcutaneous treatment (study drug) and a placebo
• Reimbursement for study-related expenses may be provided

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For more information about this trial, please visit ClinicalTrials.gov

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Last Revised: July 2024

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Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
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Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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