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Tapinarof for the Treatment of Plaque Psoriasis in Pediatric Subjects

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NCT05172726 · readout ≤ 73 d

Sponsored by Organon and Co (industry) · OGN — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
58actual
Sites
19
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
Start2021-12-02actualWhen the study began enrolling
Primary completionOct 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionOct 2026estimatedThe whole study's end, after follow-up
First posted2021-12-29actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-17actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Plaque Psoriasis

Intervention

  • Drug: tapinarof cream, 1%

Primary outcomes

what the primary-completion date above is the date OF
Adverse Events (AEs) and Serious Adverse Events (SAEs)
measured Screening up to Week 53
Number of subjects with clinically significant laboratory test abnormalities
measured Screening up to Week 53
Number of subjects with clinically significant vital signs abnormalities
measured Screening up to Week 53
Investigator-Assessed Local Tolerability Scale (LTS) Scores
measured Baseline up to Week 52
Subject (or Caregiver)-Assessed Local Tolerability Scale (LTS)
measured Baseline up to Week 52

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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