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NCT03936335Completed

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

Study Summary

The objective of this study is to describe and compare the incidence of adverse pregnancy outcomes (spontaneous abortion/miscarriage, stillbirth) and prevalence of adverse 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.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment12343 participants
Primary Completion2026-04-13
Lead SponsorRegeneron Pharmaceuticals
Data Retrieved2026-10-14
What This Trial Means for Biotech Investors
Trial Phase Context
Status & Expected Data

This trial has completed. Results may be available via ClinicalTrials.gov or peer-reviewed publications.

Primary completion: 2026-04-13
Enrolled: 12,343 participants
Sponsor Catalyst Profile

Regeneron Pharmaceuticals (REGN) is the sponsoring company for this trial. BiotechSign currently grades this company C (52/100) based on composite catalyst signals across its full pipeline. This trial is one data point in that overall catalyst picture.

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