Observational Study of Patients Receiving Dupixent® for Atopic Dermatitis (AD)

Korábbi kezelés

• Participants who have a contraindication to the drug according to the country-specific prescribing information label
• Prior use of Dupixent® within 6 months of the screening visit, or within 6 months of the baseline visit if screening and baseline occur on the same day
  • The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Más betegség

• Any condition that, in the opinion of the investigator, may interfere with patient's ability to participate in the study, such as short life expectancy, substance abuse, severe cognitive impairment, or other co-morbidities that can predictably prevent the participant patient from adequately completing the schedule of visits and assessments

Egyéb

• Patients currently participating in any interventional clinical trial which modifies patient care

• Male or female, 12 years or older at the baseline visit. Note: Adolescent participants (at least 12 years old, but less than 18 years) are eligible only after Dupixent® receives the respective country's regulatory approval for use in this age group;
• Initiating treatment with Dupixent® for AD according to the country-specific prescribing information. Note: Participants may be eligible if they have already initiated treatment with Dupixent® for AD within 6 months before their enrollment in the registry, provided that all core baseline data required (Eczema Area and Severity Index \[EASI\], Scoring of Atopic Dermatitis \[SCORAD\], body surface area \[of AD involvement\] \[BSA\], Patient-Oriented Eczema Measure \[POEM\], and Dermatology Life Quality Index \[DLQI\]) by the registry protocol were captured at the time of initiating Dupixent® treatment and are available for entry in the registry database
• Able to understand and complete study-related questionnaires
• Provide signed informed consent or parental/legally acceptable representative consent and/or patient assent where applicable