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NCT07007091 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study of Healthy Volunteers, sponsored by AbbVie.

Completed
Registry status
Phase 1
Development phase
260
Enrollment target
4
Study locations

NCT07007091 is a Phase 1 study of Healthy Volunteers that has completed, run by AbbVie. The registered enrollment target is 260 participants, below the 481-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (46% lower). The trial reports 4 study locations across 4 states.

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The verdict

NCT07007091, a Phase 1 study of Healthy Volunteers, has completed, sponsored by AbbVie.

COMPLETED
Registry status
Phase 1
Development phase
260 participants
Enrollment target
4
Study locations

Study Summary

This study will assess the pharmacokinetics and relative Bioavailability of risankizumab following subcutaneous administration with an on-body injector relative to a prefilled syringe

Conditions Studied

Interventions

  • DRUG Risankizumab

Study Locations (4)

Florida

  • Cpmi /Id# 276490 - Miami

Illinois

  • Acpru /Id# 276043 - Grayslake

Nevada

  • Ppd - Las Vegas Research Unit /ID# 276565 - Las Vegas

Texas

  • PPD Phase I Clinic /ID# 276525 - Austin

Trial Details

FieldValue
Enrollment Target 260 participants
Start Date 2025-06-12
Est. Completion 2026-01-15
Phase Phase 1

Sponsor

AbbVie

526 total trials

What the Registry Record Tells You About NCT07007091

The ClinicalTrials.gov registry entry for NCT07007091 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 260 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 481-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (46% lower). The listed sponsor is AbbVie, which has 526 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy Volunteers appearing as the primary indexed condition, and to 1 intervention - of which Risankizumab is the first listed.

NCT07007091 reports 4 study locations spanning 4 distinct geographic areas - top geographies include Florida, Illinois, Nevada.

Frequently Asked Questions

What is clinical trial NCT07007091 about?

NCT07007091 is a clinical study titled "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". This study will assess the pharmacokinetics and relative Bioavailability of risankizumab following subcutaneous administration with an on-body injector relative to a prefilled syringe

What is the current status of trial NCT07007091?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 260 participants. The study started on 2025-06-12. Estimated completion is 2026-01-15.

What conditions does trial NCT07007091 study?

This clinical trial studies the following conditions: Healthy Volunteers.

What interventions are being tested in trial NCT07007091?

The interventions under investigation include: Risankizumab (DRUG).

Who is sponsoring clinical trial NCT07007091?

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

Where is trial NCT07007091 being conducted?

This trial has 4 study locations across Florida, Illinois, Nevada, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.