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A Study With Self-administered Rocatinlimab in Adolescent and Adult Participants With Moderate-to-severe Atopic Dermatitis

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NCT06224192

Sponsored by Amgen (industry) · AMGN — their whole pipeline →.

Phase
Phase 3
Status
Completed
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
151actual
Sites
47
Countries
Canada, Japan, South Korea +1

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
Start2024-04-02actualWhen the study began enrolling
Primary completion2025-04-11actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-03-16actualThe whole study's end, after follow-up
First posted2024-01-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-03-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Atopic Dermatitis

Interventions

  • Combination product: Rocatinlimab Prefilled Syringe — also filed as AMG 451
  • Combination product: Rocatinlimab AI — also filed as AMG 451

Primary outcome

what the primary-completion date above is the date OF
Proportion of Full-dose Self-administered Rocatinlimab Injections Among Total Attempted Injections up to Week 16
measured Up to Week 16

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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