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Trials / Active Not Recruiting

Active Not RecruitingNCT06099704

Observational Study of Canadian Patients (6 Years or Older) Receiving Dupixent® for Moderate to Severe Atopic Dermatitis

A Prospective, Observational Study of Canadian Patients Receiving Dupixent® for Moderate to Severe Atopic Dermatitis

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
305 (actual)
Sponsor
Sanofi · Industry
Sex
All
Age
6 Years
Healthy volunteers
Not accepted

Summary

This is a prospective, 18-month observational study of adult, adolescent and pediatric Canadian participants with Atopic Dermatitis (AD) commonly known as Eczema, who receive treatment with Dupixent for moderate-to-severe AD (msAD) according to the Canadian-specific prescribing information (in accordance with the Canadian Dupixent Product Monograph). The study will be conducted in approximately 30 centers in Canada to assess participants of all ethnicities and races. At each participating site, all AD participants who receive an initial prescription for Dupixent will be invited to participate in this study, until the Canadian enrollment goal is achieved.

Detailed description

The duration of the study for each participant will be of 18 months.

Conditions

Timeline

Start date
2023-10-10
Primary completion
2026-04-10
Completion
2026-04-10
First posted
2023-10-25
Last updated
2025-03-18

Locations

29 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT06099704. Inclusion in this directory is not an endorsement.