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Study of Patients Receiving DUPIXENT® for Atopic Dermatitis (AD)

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NCT03428646 · readout in 223 d

Sponsored by Regeneron Pharmaceuticals (industry) · REGN — their whole pipeline →. With Sanofi.

Phase
Status
Active, not recruiting
Study type
Observational
Enrollment
858actual
Sites
99
Countries
Canada, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2018-04-06actualWhen the study began enrolling
Primary completion2027-03-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-03-30estimatedThe whole study's end, after follow-up
First posted2018-02-09actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-12-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Dermatitis, Atopic

Intervention

  • Drug: Dupilumab — also filed as DUPIXENT®, REGN668

Primary outcomes

what the primary-completion date above is the date OF
Registry Assessment: Baseline Characteristics
measured At baseline (day when DUPIXENT treatment is initiated)
Registry Assessment: Baseline Characteristic
measured At baseline (day when DUPIXENT treatment is initiated)

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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