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Hidradenitis Suppurativa Study (60 Weeks)

For condition: Hidradenitis Suppurativa
Enrolling:
DRI19220

Hidradenitis Suppurativa Study (60 Weeks)

Study Summary

Who Can Participate?
Male or female aged 18 or above with hidradenitis suppurativa (HS) may participate.

Inclusion Criteria
• Diagnosis of moderate to severe HS for at least 6 months
• Must have HS lesions present in at least 2 distinct anatomic areas

Participant Information
• Participate and receive study treatment at no cost
• Regular visits with study doctors who specialise in treating hidradenitis suppurativa (28 visits)
• Will receive either an investigative subcutaneous (SC) injection treatment (study drug) or 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

Introductions

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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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Changes to the Policy

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

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