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A Study to Assess the Relative Bioavailability of Risankizumab Following Subcutaneous Administrations With a Pre-Filled Syringe or an On-Body Injector in Healthy Adult Participants

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NCT07007091

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · None · Basic science
Enrollment
260actual
Sites
4
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
Start2025-06-12actualWhen the study began enrolling
Primary completion2026-01-15actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-01-15actualThe whole study's end, after follow-up
First posted2025-06-05actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-01-27actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Volunteers

Interventions

  • Drug: Risankizumab
  • Drug: Risankizumab

Primary outcomes

what the primary-completion date above is the date OF
Maximum Observed Plasma Concentration (Cmax) of Risankizumab
measured Up to Approximately 113 days
Time to Cmax (Tmax) of Risankizumab
measured Up to Approximately 113 days
Apparent Terminal Phase Elimination Rate Constant (β) of Risankizumab
measured Up to Approximately 113 days
Terminal Phase Elimination Half-life (t1/2) of Risankizumab
measured Up to Approximately 113 days
Area Under the Plasma Concentration-Time Curve (AUC) From Time 0 to the Last Measurable Concentration (AUCt) of Risankizumab
measured Up to Approximately 113 days
Area Under the Plasma Concentration-Time Curve (AUC) From Time 0 to Infinity (AUCinf) of Risankizumab
measured Up to Approximately 113 days
Number of Anti-drug antibodies (ADA)
measured Up to Approximately 113 days
Number of Participants Experiencing Adverse Events
measured Up to Approximately 113 days

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