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Clinical Trial Summary

Primary Objective: To demonstrate the efficacy of dupilumab in adult and adolescent participants with primary acquired chronic inducible cold urticaria (ColdU) who remain symptomatic despite the use of an H1-antihistamine Secondary Objectives: To demonstrate the efficacy of dupilumab on primary acquired chronic inducible ColdU disease control To demonstrate the efficacy of dupilumab on primary acquired chronic inducible ColdU local signs and symptoms (hives/wheals, itch, burning sensation and pain) after provocation test To demonstrate the efficacy of dupilumab on primary acquired chronic inducible ColdU disease activity To demonstrate improvement in health-related quality-of-life and overall disease status and severity To evaluate the ability of dupilumab in reducing the proportion of participants who require rescue therapy To evaluate the proportion of participants with cold exposure triggered urticaria To evaluate safety outcome measures To evaluate immunogenicity of dupilumab


Clinical Trial Description

The duration of study for each participant included 2-4 weeks of screening period, 24 weeks of treatment period and 12 weeks of post treatment period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04681729
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 3
Start date December 10, 2020
Completion date April 20, 2023

See also
  Status Clinical Trial Phase
Completed NCT04548869 - A Single Dose Study of the Safety, Pharmacokinetics and Pharmacodynamics of CDX-0159 in Patients With Cold Contact Urticaria, Symptomatic Dermographism, or Cholinergic Urticaria Phase 1
Terminated NCT04513548 - Study of Mechanism of Action of Ligelizumab (QGE031) in Patients With Chronic Urticaria Phase 1
Recruiting NCT05960708 - A Single Dose, Phase 1 Study of YH35324 in Patients With Various Allergic Diseases Phase 1