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Clinical Trials in the USA / NCT05662241
Active, not recruiting Phase 3

A Phase 3 Study of Obexelimab in Patients With IgG4-Related Disease

NCT05662241 · tracked via the Priya Life Science USA tracker
Sponsor
Zenas BioPharma (USA), LLC
Phase
Phase 3
Started
2023-01-09
Last updated
2026-02-04

Condition(s) studied

IgG4 Related Disease

Investigational drug(s) / intervention(s)

ObexelimabPlacebo

Obexelimab: Obexelimab is a monoclonal antibody that co-engages CD19 and FcγRIIb to inhibit B cell activity

Placebo: Placebo

Study summary

This study aims to examine the efficacy and safety of obexelimab for the prevention of flare of IgG4-related disease (IgG4-RD)

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Males and females, ≥ 18 years of age 2. Clinical diagnosis of IgG4-RD 3. Patients must meet the 2019 ACR/EULAR Classification Criteria for IgG4-RD 4. Patients must have active IgG4-RD signs/symptoms (i.e., flare) that require the initiation of GC therapy or the increase in background long-term GC therapy 5. Other inclusion criteria apply Exclusion Criteria: 1. Has disease in only 1 organ system whose primary manifestation is fibrosis 2. Has received prednisone equivalent given orally at a dose greater than 60 mg/day within the 4 weeks prior to screening or during screening 3. Has received a non-biologic, disease-modifying anti-rheumatological drug or immunosuppressive agent other than GCs within the 2 weeks prior to screening 4. Has received an investigational treatment or direct medical intervention on another clinical study within 12 weeks or \< 5 half-lives of the investigational treatment, whichever is shorter, prior to screening 5. Has received live vaccine or live therapeutic infectious agent within the 2 weeks prior to screening 6. Active tuberculosis or high risk for tuberculosis; hepatitis C infection in absence of curative treatment; evidence of hepatitis B infection 7. Use of B cell depleting or targeting agents within 6 months of randomization 8. Other exclusion criteria apply

Primary outcome measure(s)

Trial sites (65)

FacilityCityRegionStatus
Stanford Medicine Stanford California
GI PROS Research - Dedicated Research Facility Naples Florida
Emory Univeristy Atlanta Georgia
Massachusetts General Hospital Boston Massachusetts
Henry Ford Hospital Detroit Michigan
Hospital Italiano de Buenos Aires Buenos Aires Argentina
Artus Health Centre Vancouver British Columbia
Center for Clinical Research (Nova Scotia Health) Halifax Nova Scotia
Centre Hospitalier Universitaire de Sherbrooke CHUS Sherbrooke Quebec
Chinese PLA General Hospital Beijing Beijing Municipality
Peking Union Medical College Hospital Beijing Beijing Municipality
Peking University First Hospital Beijing Beijing Municipality
The Second Hospital of Hebei Medical University Shijiazhuang Hebei
Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology Wuhai Hubei
Yantai Yuhuangding Hospital Yantai Shandong
Renji Hospital, Shanghai Jiaotong University School of Medicine Shanghai Shanghai Municipality
Shanxi Bethune Hospital Taiyuan Shanxi
West China Hospital of Sichuan University Chengdu Sichuan
Haut-Lévèque Hospital Usn Building South Hospital Group Pessac Bordeaux
Hôpitaux Universitaires de Marseille Timone Saint-Pierre Marseille
Hôpital Beaujon Paris France
Hôpital de la Pitié Salpétrière Paris France
LMU Klinikum der Universität München München Bavaria
Universitätsklinikum Ulm Ulm Germany
Ospedale San Giovanni Bosco Turin Piedmont
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia Brescia Italy
Azienda Ospedaliera Universitaria Meyer Istituto di Ricovero e Cura a Carattere Scientifico Florence Italy
Ospedale San Raffaele S.r.l. - PPDS Milan Italy
University of Verona Verona Italy
Hospital of University of Occupational and Environmental Health Kitakyushu Fukuoka
Kanazawa Medical University Hospital Kokura Fukuoka
Kanazawa University Hospital Kanazawa Ishikawa-ken
Kagawa University Hospital Hiragi Kagawa-ken
Shinshu University Hospital Matsumoto Nagano
Osaka Metropolitan University Hospital Osaka Osaka
Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital Bunkyō-Ku Tokyo
The Institute of Medical Science, The University of Tokyo Hospital Minato-ku Tokyo
Keio University Hospital Shinjuku-Ku Tokyo
Toyama University Hospital Toyama Toyama
Kansai Medical University Hospital Hirakata Japan

+ 25 more sites — see the full list on the official registry below.

More Zenas BioPharma (USA), LLC trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05662241 on ClinicalTrials.gov ↗ ← All trials in the USA