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Research Trial for Chronic Spontaneous Urticaria 1 (72 Weeks)-CA

For condition: Chronic Spontaneous Urticaria
For condition: Urticaria
Enrolling:
CDX0159-12

Research Trial for Chronic Spontaneous Urticaria 1 (72 Weeks)-CA

Study Summary

Who Can Participate?

Males or females, ≥ 18 years of age with chronic spontaneous urticaria (CSU) may be eligible to participate.

 

Inclusion Criteria:

      • Diagnosis of CSU for 6 months or more
      • CSU resistant to a stable dose and regimen containing a second-generation H1 antihistamine (H1AH), as defined by the following:
      • Recurrent pruritic wheals (itchy bumps) with or without angioedema (swelling in deeper layers of skin) for ≥ 6 weeks at any time prior to screening despite treatment with a H1AH
      • Must have been on a stable dose and regimen containing a second-generation H1AH at approved or increased dose as background therapy for the treatment of CSU for ≥ 4 weeks prior to randomization

 

Participant Info:

      • No cost to participate or receive treatment
      • Regular visits with study doctors who specialise in treating chronic spontaneous urticaria
      • Will receive investigational injected treatment (active study drug) or placebo
      • Reimbursement for study-related expenses may be provided

 

How Long Will The Study Last?

      • 72 weeks (19 study visits)
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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
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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Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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