Back to Trials
NCT07466550PHASE1RecruitingAccepts Healthy Volunteers

A Study to Assess How Intravenous and Subcutaneous Administrations of Risankizumab Moves Through the Body of Healthy Adult Participants

AbbVie

Start Date

6/4/2026

Completion Date

1/1/2027

Summary

The purpose of this study is to compare how the drug moves through the body following risankizumab subcutaneous (SC) and risankizumab intravenous (IV) doses.

Eligibility Criteria

Age Range: 18 years to 65 years

Inclusion Criteria: * Body weight between 40 kg and 100 kg inclusive at screening and upon initial confinement. * BMI is ≥ 18.0 to ≤ 32.0 kg/m2 after rounding to the tenths decimal at Screening. BMI is calculated as weight in kg divided by the square of height measured in meters. * A condition of general good health, based upon the results of a medical history, physical examination, vital signs, laboratory profile and a 12-lead ECG. Exclusion Criteria: * Exposure to any anti-interleukin-12/23 or anti interleukin-23 treatment for at least one year prior to Screening. * Intention to perform strenuous exercise to which the subject is unaccustomed within one week prior to administration of first dose of study treatment or during the study.

Interventions

DRUG

Risankizumab

DRUG

Risankizumab

Interested in This Trial?

Contact the trial locations directly using the information below to learn more about enrollment.

Expressing interest lets you review the study and consent before we connect you with the research site.

Conditions

Healthy Volunteer

Locations

CenExel ACT- Anaheim Clinical Trials /ID# 281821

Anaheim, California 92801

United States

Cpmi /Id# 281783

Miami, Florida 33172

United States