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

← catalyst calendar

NCT03992417 · readout in 224 d

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

Phase
Status
Active, not recruiting
Study type
Observational
Enrollment
955actual
Sites
105
Countries
Argentina, Australia, Austria +19

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
Start2019-06-11actualWhen the study began enrolling
Primary completion2027-03-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-03-31estimatedThe whole study's end, after follow-up
First posted2019-06-20actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-06actualThe 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 SAR231893 (REGN668) — also filed as Dupixent®

Primary outcomes

what the primary-completion date above is the date OF
Baseline Characteristics: Medical history
measured Baseline to Month 60
Baseline Characteristics: Socio-demographics
measured Baseline to Month 60
Baseline Characteristics: Disease characteristics
measured Baseline to Month 60

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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