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A Study to Evaluate Dermal Open-Flow Microperfusion and Plasma Pharmacokinetic Study of Multiple Doses of Oral Povorcitinib or Topical Ruxolitinib Cream in Healthy Adult Participants

← catalyst calendar

NCT07588139 · readout in 15 d

Sponsored by Incyte Corporation (industry) · INCY — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
24estimated
Sites
1
Country
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
Start2026-05-18actualWhen the study began enrolling
Primary completion2026-09-03estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-09-19estimatedThe whole study's end, after follow-up
First posted2026-05-14actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Participants

Interventions

  • Drug: Povorcitinib — also filed as INCB054707
  • Drug: Ruxolitinib

Primary outcomes

what the primary-completion date above is the date OF
Pharmacokinetics Parameter (PK): Cmax of dermal interstitial fluid (dISF) ruxolitinib
measured Up to Day 12
Pharmacokinetics Parameter: AUClast of dISF ruxolitinib
measured Up to Day 12
Pharmacokinetics Parameter: AUC∞ of dISF ruxolitinib
measured Up to Day 12
Pharmacokinetics Parameter: Cmax of dISF povorcitinib
measured Up to Day 12
Pharmacokinetics Parameter: AUClast of dISF povorcitinib
measured Up to Day 12
Pharmacokinetics Parameter: AUC∞ of dISF povorcitinib
measured Up to Day 12
Pharmacokinetics Parameter: Cmax of plasma ruxolitinib
measured Up to Day 12
Pharmacokinetics Parameter: AUClast of plasma ruxolitinib
measured Up to Day 12
Pharmacokinetics Parameter: AUC∞ of plasma ruxolitinib
measured Up to Day 12
Pharmacokinetics Parameter: Cmax of plasma povorcitinib
measured Up to Day 12
Pharmacokinetics Parameter: AUClast of plasma povorcitinib
measured Up to Day 12
Pharmacokinetics Parameter: AUC∞ of plasma povorcitinib
measured Up to Day 12

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