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NCT06946524 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess the Bioavailability of Risankizumab Following Subcutaneous Administration With Prefilled Pen Relative to a Prefilled Syringe in Healthy Adult Participants

A Phase 1 study, sponsored by AbbVie.

Completed
Registry status
Phase 1
Development phase
59
Enrollment target

NCT06946524: Completed Phase 1 study, sponsored by AbbVie.

NCT06946524 is a Phase 1 study that has completed, run by AbbVie. The registered enrollment target is 59 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06946524, a Phase 1 study, has completed, sponsored by AbbVie.

COMPLETED
Registry status
Phase 1
Development phase
59 participants
Enrollment target

Study Summary

This study will assess the pharmacokinetics, relative bioavailability, immunogenicity, safety, and tolerability of risankizumab following subcutaneous (SC) administration with a prefilled pen or a prefilled syringe in healthy adult participants.

Primary Outcome

Maximum observed plasma concentration (Cmax) of Risankizumab

Interventions

  • DRUG Risankizumab

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2025-05-08
Est. Completion 2025-11-25
Phase Phase 1
AbbVie

526 total trials

What the finished NCT06946524 record still lists

NCT06946524 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

The record links to 0 conditions, and to 1 intervention - of which Risankizumab is the first listed.

NCT06946524 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06946524 about?

NCT06946524 is a clinical study titled "A Study to Assess the Bioavailability of Risankizumab Following Subcutaneous Administration With Prefilled Pen Relative to a Prefilled Syringe in Healthy Adult Participants". This study will assess the pharmacokinetics, relative bioavailability, immunogenicity, safety, and tolerability of risankizumab following subcutaneous (SC) administration with a prefilled pen or a prefilled syringe in healthy adult participants.

What is the current status of trial NCT06946524?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 59 participants. The study started on 2025-05-08. Estimated completion is 2025-11-25.

What interventions are being tested in trial NCT06946524?

The interventions under investigation include: Risankizumab (DRUG).

Who is sponsoring clinical trial NCT06946524?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06946524's enrollment target sits among peer trials

59 895th of 2000 higher than 1,106 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06946524, the US trial registry maintained by the National Library of Medicine. NCT06946524 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.