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Adult’s Hidradenitis Suppurativa Study (61 Weeks)

For condition: Hidradenitis Suppurativa
Enrolling:
TAK-279-HS-2001

Adult’s Hidradenitis Suppurativa Study (61 Weeks)

Study Summary

Who Can Participate?
People aged 18 and above with moderate to severe Hidradenitis Suppurativa (HS) may participate.

Inclusion Criteria

  • Participants must have signs and symptoms of HS for at least 6 months
  • Diagnosis of HS, with stable HS signs and symptoms for 2 months
  • Participants must have a history of inadequate response to a previous course of oral antibiotic for treatment of HS or exhibited recurrence, intolerance, or contraindication during that course of oral antibiotic

Participant Information

  • Participate and receive study treatment at no cost
  • Regular visits with study doctors who specialise in treating Hidradenitis Suppurativa (up to 12 visits)
  • Will receive either an investigative oral treatment (study drug) or a placebo
  • Reimbursement for study-related expenses may be provided

How Long Will The Study Last?

  • Approximately 61 weeks
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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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Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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