Skip to main content
Clinical Trials/EUCTR2018-004705-26-DE
EUCTR2018-004705-26-DE
Active, not recruiting
Phase 1

A randomized double blind placebo controlled study evaluating the effect of dupilumab on sleep in adult patients with moderate to severe atopic dermatitis - DUPISTAD

Sanofi Aventis Groupe0 sites268 target enrollmentJanuary 22, 2020

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Sanofi Aventis Groupe
Enrollment
268
Status
Active, not recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 22, 2020
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Participants, male or female 18 years or older,
  • \- with diagnosed chronic atopic dermatitis (AD), demonstrated 1\) inadequate response to topical medications, 2\) expected severity of AD and 3\) sleep disturbance
  • \- having applied skin emolients (moisturizers) at least 7 days before randomization
  • \- having applied medium potency topical corticosteroids (TCS) on all active AD lesions at least 7 days before randomization
  • \- willing and able to comply with all clinic visits and study\-related procedures
  • \- providing signed informed consent
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 253

Exclusion Criteria

  • Participants excluded from the study:
  • \- with known hypersensitivity to Dupixent, clinical depression, drug abuse history, sleep problems not related to AD, irregular sleep pattern, active/acute infections, severe medical conditions, laboratory abnormalities, any condition that may present unreasonable risk to patients or interfere with study assessment, or any severe concomitant illness(es) that would adversely affect the patient's participation in the study, and contraindications of topical corticosteroids
  • \- at baseline, presence of any conditions listed as criteria for study drug discontinuation
  • The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial

Outcomes

Primary Outcomes

Not specified

Similar Trials