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RECRUITING
NCT06977724
PHASE1

A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effectiveness of Intravenous Infusions of ABBV-319 in Adult Participants With Systemic Lupus Erythematosus (SLE), Sjogren's Disease (SjD) and Rheumatoid Arthritis (RA)

Sponsor: AbbVie

View on ClinicalTrials.gov

Summary

Systemic lupus erythematosus (SLE) is a chronic, systemic autoimmune disease characterized by B cell hyperactivity. Sjorgren's disease (SjD) is a chronic, multisystem autoimmune disease characterized by lacrimal and salivary gland inflammation, with resultant dryness of the eyes and mouth and occasional glandular enlargement and Rheumatoid arthritis (RA) is a long-lasting autoimmune disease that causes the body's immune system to attack itself. RA targets the body's joints, causing inflammation (swelling, pain, and redness). ABBV-319 exhibits potential B cell depletion in SLE, SjD and RA which are characterized by B cell hyperactivity. The purpose of this study is to assess the pharmacokinetics, safety, and efficacy of ABBV-319 in adult participants with SLE, SjD and RA. ABBV-319 is an investigational drug being developed for the treatment of SLE , SjD and RA. Participants are placed in 1 of 8 groups called treatment arms. Each group receives a different dose of ABBV-319 depending on whether they have SLE, SjD or RA. Around 48 adult participants with SLE, SjD or RA will be enrolled at approximately up to 17 sites worldwide. Participants will receive 2 doses of IV ABBV-319 21 days apart and will be followed for up to 343 days. There may be higher treatment burden for participants in this trial compared to their standard of care (due to study procedures). Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.

Official title: A Phase1b, Multiple Ascending Dose, Open-label, Non-randomized Study Evaluating the Pharmacokinetics, Safety, and Efficacy of ABBV-319 in Subjects With Systemic Lupus Erythematosus (SLE), Sjogren's Disease (SjD) and Rheumatoid Arthritis (RA)

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

36

Start Date

2025-08-26

Completion Date

2029-03

Last Updated

2026-08-10

Healthy Volunteers

No

Interventions

DRUG

ABBV-319

Intravenous (IV) Infusion

Locations (11)

Highlands Advanced Rheumatology And Arthritis Center - Avon Park /ID# 278239

Avon Park, Florida, United States

Clinical Research Of West Florida - Phase I Unit /ID# 275834

Clearwater, Florida, United States

Life Clinical Trials - Colonial Drive - Margate /ID# 276050

Margate, Florida, United States

Clinical Research Of West Florida - Tampa - North Howard Avenue /ID# 275836

Tampa, Florida, United States

Advanced Quality Medical Research /ID# 278462

Orland Park, Illinois, United States

Private Practice - Dr. Ramesh C. Gupta /ID# 275826

Memphis, Tennessee, United States

Integrative Rheumatology of South Texas - Harlingen /ID# 276458

Harlingen, Texas, United States

Les Hopitaux Universitaires de Strasbourg - Hopital de Hautepierre /ID# 272692

Strasbourg, Alsace, France

CHU de Montpellier - Hopital Lapeyronie /ID# 279892

Montpellier, Herault, France

Amsterdam University Medical Center /ID# 274286

Amsterdam, North Holland, Netherlands

Universitair Medisch Centrum Utrecht /ID# 273398

Utrecht, Netherlands