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An Observational Retrospective Cohort Study Being Conducted in Women With Atopic Dermatitis (AD)

Recruiting
18 - 49 years of age
Female
Phase N/A
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Overview

The objective of this study is to describe and compare the incidence of adverse pregnancy outcomes (spontaneous abortion/miscarriage, stillbirth) and prevalence of infant outcomes (major congenital malformations [MCMs], small for gestational age [SGA]) in women with AD who are treated with dupilumab during pregnancy relative to women with AD who are not treated with dupilumab during pregnancy.

Eligibility

Key Inclusion Criteria:

  • Continuous medical and pharmacy benefit coverage for at minimum 6 months prior to and including the estimated LMP
  • Diagnosis code indicative of AD in the period from up to 1 year prior to the estimated LMP through the end of the pregnancy

Note: Other Protocol Defined Inclusion / Exclusion Criteria Apply

Study details

Adverse Pregnancy Outcomes, Atopic Dermatitis

NCT03936335

Regeneron Pharmaceuticals

27 January 2024

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