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A Long-term Extension Study of Apremilast (CC-10004) in Pediatric Subjects From 6 Through 17 Years of Age With Moderate to Severe Plaque Psoriasis

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NCT04175613

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

Phase
Phase 3
Status
Completed
Study type
Interventional
Design
Na · None · Treatment
Enrollment
160actual
Sites
50
Countries
Belgium, Canada, Czechia +6

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
Start2019-12-20actualWhen the study began enrolling
Primary completion2025-10-30actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-12-12actualThe whole study's end, after follow-up
First posted2019-11-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-12-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Psoriasis

Intervention

  • Drug: Apremilast — also filed as CC-10004, Otezla

Primary outcomes

what the primary-completion date above is the date OF
Adverse Events (AEs)
measured Up to approximately 4 years
Columbia-Suicide Severity Rating Scale (C-SSRS)
measured Collected at each study visit throughout the life of the study - up to 4 years
Weight of patients treated with Apremilast
measured Collected at each study visit throughout the life of the study - up to 4 years
Mean body mass index of the patient treated with Apremilast
measured Collected at each study visit throughout the life of the study - up to 4 years
Height patients treated with Apremilast
measured Collected at each study visit throughout the life of the study - up to 4 years
Assessment of sexual maturity
measured Collected every 52 weeks throughout the life of the study - up to 4 years

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