Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effects of EP262 in Subjects With Chronic Spontaneous Urticaria
Chronic Spontaneous UrticariaPhase 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
William Yang
Evidence Based Medical Educator Inc
Evidence Based Medical Educator IncToronto, Ontario
Canada
Contact Study Team
Jason Lee
Centre de Recherche Saint-Louis
Centre de Recherche Saint-LouisQuébec, Quebec
Canada
Contact Study Team
- Study Sponsored By
- Escient Pharmaceuticals, Inc
- Participants Required
- More Information
- Study ID:
NCT06077773