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Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effects of EP262 in Subjects With Chronic Spontaneous Urticaria

Chronic Spontaneous Urticaria

Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effects of EP262 in Subjects with Chronic Spontaneous Urticaria

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 to 80

Participation Criteria

Inclusion Criteria:

* Documented history of chronic spontaneous urticaria (CSU) with a UAS7 greater than or equal to 16 despite stable treatment with H1 antihistamine consistent with standard of care
* Must be on a stable dose of H1 antihistamine up to 4 times the approved dose per local treatment guidelines

Exclusion Criteria:

* Urticaria with a clear underlying etiology other than CSU
* Urticaria with a clearly defined or sole trigger (chronic inducible urticaria)
* Other active skin diseases associated with chronic pruritus (eg, atopic dermatitis, bullous pemphigoid, prurigo nodularis, dermatitis herpetiformis)

Study Location

Red Maple Trials Inc.
Red Maple Trials Inc.
Ottawa, Ontario
Canada

Contact Study Team

Primary Contact

William Yang

Evidence Based Medical Educator Inc
Evidence Based Medical Educator Inc
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Jason Lee

Centre de Recherche Saint-Louis
Centre de Recherche Saint-Louis
Québec, Quebec
Canada

Contact Study Team

Study Sponsored By
Escient Pharmaceuticals, Inc
Participants Required
More Information
Study ID: NCT06077773