A Study of Ustekinumab in Participants With Active Systemic Lupus Erythematosus

NCT ID: NCT03517722

Last Updated: 2025-04-29

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE3

Total Enrollment

516 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-04-16

Study Completion Date

2020-11-05

Brief Summary

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The purpose of this study is to evaluate the efficacy of ustekinumab in participants with active systemic lupus erythematosus (SLE) who have not adequately responded to one or more standard of care treatments.

Detailed Description

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This study evaluates the efficacy, safety, and tolerability of ustekinumab in participants with active SLE according to Systemic Lupus International Collaborating Clinics (SLICC) criteria Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) score greater than (\>=) 6, despite receiving one or more standard-of-care treatments (example, immunomodulators, antimalarial drugs, and/or glucocorticoids). The total duration of the study is up to 182 weeks, consisting of 3 study periods: a screening period (approximately 6 weeks), a double blind period (52 weeks), and an extension period (124 weeks). Other study evaluations will include pharmacokinetics, immunogenicity, biomarkers and pharmacogenomic evaluations. The safety of the participants enrolled in the study will be monitored on an ongoing basis throughout the study.

Conditions

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Lupus Erythematosus, Systemic

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Ustekinumab

Participants will receive ustekinumab approximately 6 milligram per kilogram (mg/kg) intravenously (IV) based on body weight-range at Week 0 followed by 90 mg ustekinumab subcutaneously (SC) at Week 8 and every 8 weeks (q8w) thereafter through Week 48 during double-blind period. Eligible participants who will enter the extension period will continue to receive 90 mg ustekinumab SC q8w through Week 160.

Group Type EXPERIMENTAL

Ustekinumab (approximately 6 mg/kg)

Intervention Type DRUG

Participants will receive ustekinumab approximately 6 mg/kg via IV route based on body weight-range.

Ustekinumab 90 mg

Intervention Type DRUG

Participants will receive 90 mg ustekinumab via SC route.

Placebo

Participants will receive matching placebo to ustekinumab IV at Week 0, followed by matching placebo to ustekinumab SC at Week 8 and q8w thereafter through Week 48 during double-blind period. Eligible participants who will enter the extension period will cross-over to receive 90 mg ustekinumab SC q8w through Week 160.

Group Type EXPERIMENTAL

Placebo

Intervention Type DRUG

Participants will receive placebo matching to ustekinumab IV or SC.

Ustekinumab 90 mg

Intervention Type DRUG

Participants will receive 90 mg ustekinumab via SC route.

Interventions

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Placebo

Participants will receive placebo matching to ustekinumab IV or SC.

Intervention Type DRUG

Ustekinumab (approximately 6 mg/kg)

Participants will receive ustekinumab approximately 6 mg/kg via IV route based on body weight-range.

Intervention Type DRUG

Ustekinumab 90 mg

Participants will receive 90 mg ustekinumab via SC route.

Intervention Type DRUG

Other Intervention Names

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Stelara Stelara

Eligibility Criteria

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Inclusion Criteria

* Be male or female
* Has a documented medical history (that is, met at least 1 of the two criteria below) that participant met the Systemic Lupus International Collaborating Clinics (SLICC) classification criteria for systemic lupus erythematosus (SLE) at least 3 months prior to first dose of study agent:

1. Met a total of at least 4 SLICC criteria, including at least 1 clinical and at least 1 immunologic;
2. Has a diagnosis of lupus nephritis, confirmed by renal biopsy and at least 1 of the following autoantibodies: antinuclear antibodies (ANA) or anti-double-stranded deoxyribonucleic acid (anti-dsDNA)
* Has a positive test in the medical history and confirmed at screening for at least 1 of the following autoantibodies: antinuclear antibodies, anti-double-stranded deoxyribonucleic acid, and/or anti-Smith
* Has greater than or equal to (\>=) 1 British Isles Lupus Assessment Group (BILAG) A and/or \>= 2 BILAG B scores observed during screening
* Has a Cutaneous Lupus Erythematosus Disease Area and Severity Index (CLASI) activity score \>=4 (excluding diffuse non-inflammatory alopecia) or \>= 4 joints with pain and signs of inflammation at screening, Week 0, or both
* Has a Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) score \>=6 at screening. Must also have SLEDAI-2K \>= 4 for clinical features (excluding headache and laboratory abnormalities) at Week 0
* Cannot be pregnant, nursing, intending to become pregnant, or unwilling to follow contraception or egg/sperm donation guidelines
* Must be receiving stable doses of \>=1 protocol-permitted standard of care SLE treatment: oral glucocorticoids, anti-malarials, immunomodulators (methotrexate, azathioprine, 6-mercaptopurine, mycophenolate mofetil, mycophenolic acid)

Exclusion Criteria

* Has any unstable or progressive SLE manifestation (example: central nervous system lupus, systemic vasculitis, end-stage renal disease, severe or rapidly progressive glomerulonephritis, pulmonary hemorrhage, myocarditis) that may warrant escalation in therapy beyond permitted background medications. Participants requiring renal hemodialysis or peritoneal dialysis are also excluded
* Has other co-existent inflammatory diseases (example: rheumatoid arthritis, psoriasis, psoriatic arthritis, Crohn's disease)
* Has a urinary protein to creatinine ratio of greater than (\>)4 gram per gram (g/g) per day
* Has an acute or chronic infectious illness (example: human immunodeficiency virus, hepatitis B or C virus, tuberculosis, opportunistic infections)
* Has a history of cancer or lymphoproliferative disease within the last 5 years except for treated and non-recurrent cutaneous basal cell carcinoma, squamous cell carcinoma, or cervical carcinoma
* Has any condition requiring multiple courses of systemic glucocorticoids (example: uncontrolled asthma, chronic obstructive pulmonary disease)
* Has a history of major surgery within the last month
* Has received live virus or bacterial vaccines within 16 weeks prior to first dose of study agent or Bacille Calmette-Guerin (BCG) vaccination within 12 months of screening
* Has previously received ustekinumab
* Has received cyclophosphamide orally within 90 days or intravenously within 180 days of screening
* Has received a single B-cell targeted therapy (e.g. belimumab) within 3 months, \>1 previous B-cell targeted therapy within 6 months, or B-cell depleting therapy (example: rituximab) within 12 months of first dose of study agent
* Has received protocol-prohibited oral or biologic immunomodulatory therapy in the last 3 months or less than (\<)5 half-lives (whichever is longer) prior to first dose of study agent
* Has received adrenocorticotropic hormone (ACTH) within 1 month prior to first dose of study agent
* Has received epidural, intravenous, intramuscular, intraarticular, intrabursal, intralesional glucocorticoids within 6 weeks of first dose of study agent
* Locally-delivered therapies except for ophthalmic use of cyclosporine A or topical use of nonsteroidal anti inflammatory drugs (NSAIDs), analgesics, or high-potency glucocorticoids (World Health Organization criteria) are prohibited
Minimum Eligible Age

16 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Janssen Research & Development, LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Janssen Research & Development, LLC Clinical Trial

Role: STUDY_DIRECTOR

Janssen Research & Development, LLC

Locations

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Pinnacle Research Group, LLC

Anniston, Alabama, United States

Site Status

University of Alabama at Birmingham

Birmingham, Alabama, United States

Site Status

Achieve Clinical Research, LLC

Vestavia Hills, Alabama, United States

Site Status

Medvin Clinical Research

Covina, California, United States

Site Status

Lugene Eye Institute

Glendale, California, United States

Site Status

C.V. Mehta, MD Medical Corp.

Hemet, California, United States

Site Status

University of California at San Diego

La Jolla, California, United States

Site Status

Advanced Medical Research - Lakewood

Lakewood, California, United States

Site Status

Loma Linda University

Loma Linda, California, United States

Site Status

Loma Linda University Health Care

Loma Linda, California, United States

Site Status

Valerius Medical Group & Research Center

Los Alamitos, California, United States

Site Status

Keck School of Medicine of USC

Los Angeles, California, United States

Site Status

Wallace Rheumatic Study Center

Los Angeles, California, United States

Site Status

East Bay Rheumatology Medical Group

San Leandro, California, United States

Site Status

Westlake Medical Research Clinical Trials

Thousand Oaks, California, United States

Site Status

University Clinical Investigators, Inc

Tustin, California, United States

Site Status

Inland Rheumatology Clinical Trials Inc.

Upland, California, United States

Site Status

University of Colorado

Aurora, Colorado, United States

Site Status

Denver Arthritis Clinic

Denver, Colorado, United States

Site Status

UPMC Lupus Center of Excellence

New Haven, Connecticut, United States

Site Status

Stamford Therapeutics Consortium

Stamford, Connecticut, United States

Site Status

Arthritis and Rheumatic Disease Specialties

Aventura, Florida, United States

Site Status

Bay Area Arthritis and Osteoporosis

Brandon, Florida, United States

Site Status

Centre for Rheumatology, Immunology and Arthritis

Fort Lauderdale, Florida, United States

Site Status

University of Florida Health Jacksonville

Jacksonville, Florida, United States

Site Status

University of Miami Miller School of Medicine

Miami, Florida, United States

Site Status

New Horizon Research Center

Miami, Florida, United States

Site Status

Rheumatology Associates of Central Florida, PA

Orlando, Florida, United States

Site Status

Omega Research Consultants

Orlando, Florida, United States

Site Status

Millennium Research

Ormond Beach, Florida, United States

Site Status

Integral Rheumatology And Immunology Specialists

Plantation, Florida, United States

Site Status

Clinical Research of West Florida

Tampa, Florida, United States

Site Status

Emory University

Atlanta, Georgia, United States

Site Status

Piedmont Healthcare - Piedmont Hospital

Atlanta, Georgia, United States

Site Status

DeKalb Medical Specialty Center

Decatur, Georgia, United States

Site Status

Rush University Medical Center

Chicago, Illinois, United States

Site Status

University of Chicago

Chicago, Illinois, United States

Site Status

Graves-Gilbert Clinic - Bowling Green

Bowling Green, Kentucky, United States

Site Status

Arthritis and Diabetes Clinic

Monroe, Louisiana, United States

Site Status

The Center for Rheumatology and Bone Research

Wheaton, Maryland, United States

Site Status

June DO, PC.

Lansing, Michigan, United States

Site Status

St Paul Rheumatology PA

Eagan, Minnesota, United States

Site Status

University of Mississippi Medical Center

Jackson, Mississippi, United States

Site Status

Oklahoma Medical Research Foundation

Las Vegas, Nevada, United States

Site Status

Innovative Health Research

Las Vegas, Nevada, United States

Site Status

Albuquerque Center for Rheumatology

Albuquerque, New Mexico, United States

Site Status

Biomedical Research Alliance Of New York

Lake Success, New York, United States

Site Status

The Feinstein Institute for Medical Research

Manhasset, New York, United States

Site Status

NYU Center for Musculoskeletal Care

New York, New York, United States

Site Status

Hospital for Special Surgery

New York, New York, United States

Site Status

SUNY Upstate Medical University

Syracuse, New York, United States

Site Status

Joint and Muscle Research Institute

Charlotte, North Carolina, United States

Site Status

DJL Clinical Research, PLLC

Charlotte, North Carolina, United States

Site Status

Duke University Medical Center

Durham, North Carolina, United States

Site Status

Wake Forest Baptist Medical Center

Winston-Salem, North Carolina, United States

Site Status

OK Center for Arthritis Therapy & Research, Inc.

Tulsa, Oklahoma, United States

Site Status

Lewis Katz School of Medicine, Temple University

Philadelphia, Pennsylvania, United States

Site Status

Allegheny Rheumatology/Allegheny Singer Research Institute

Wexford, Pennsylvania, United States

Site Status

Columbia Arthritis Center

Columbia, South Carolina, United States

Site Status

West Tennessee Research Institute

Jackson, Tennessee, United States

Site Status

Dr. Ramesh Gupta

Memphis, Tennessee, United States

Site Status

Vanderbilt University Medical Center

Nashville, Tennessee, United States

Site Status

Amarillo Center for Clinical Research

Amarillo, Texas, United States

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Austin Regional Clinic

Austin, Texas, United States

Site Status

Arthritis Centers of Texas

Dallas, Texas, United States

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Sun Research Institute

San Antonio, Texas, United States

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UT Health Science Center at San Antonio

San Antonio, Texas, United States

Site Status

University of Washington

Seattle, Washington, United States

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Rheumatology and Pulmonary Clinic

Beckley, West Virginia, United States

Site Status

Fundacion CENIT para la Investigacion en Neurociencias

Buenos Aires, , Argentina

Site Status

Instituto Centenario

Buenos Aires, , Argentina

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Centro Privado de Medicina Familiar

Buenos Aires, , Argentina

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Framingham Centro Medico

Ciudad de La Plata, , Argentina

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Hospital Escuela 'Gral. Jose F. de San Martin'

Corrientes, , Argentina

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Hospital Italiano de Cordoba

Córdoba, , Argentina

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CER San Juan Centro Polivalente de Asistencia e Investigacion Clinica

San Juan, , Argentina

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Centro Medico Privado de Reumatologia

San Miguel de Tucumán, , Argentina

Site Status

MHAT Trimantium

Plovdiv, , Bulgaria

Site Status

Diagnostic-Consultative Center (DCC) Aleksandrovska

Sofia, , Bulgaria

Site Status

UMHAT St. Ivan Rilski

Sofia, , Bulgaria

Site Status

Medical Centre Synexus

Sofia, , Bulgaria

Site Status

University of Calgary

Calgary, Alberta, Canada

Site Status

University of Manitoba

Winnipeg, Manitoba, Canada

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McMaster University

Hamilton, Ontario, Canada

Site Status

Toronto Western Hospital

Toronto, Ontario, Canada

Site Status

CHU de Québec

Québec, Quebec, Canada

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The First Affiliated Hospital of Baotou Medical University

Baotou, , China

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Peking Union Medical College Hospital

Beijing, , China

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West China Hospital Sichuan University

Chengdu, , China

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Guangdong Provincial People's Hospital

Guangzhou, , China

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Affiliated Hospital of Inner Mongolia Med U

Hohhot, , China

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Shanghai Ruijin Hospital

Shanghai, , China

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Tianjin Medical University General Hospital

Tianjin, , China

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Tongji Hospital of Tongji Medical College of Huangzhong Univ

Wuhan, , China

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The 1st affiliated Hospital of Xi'an Traffic University

Xi'an, , China

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Centro de Investigación en Reumatología y especialidades médicas S.A.S. - CIREEM S.A.S.

Bogotá, , Colombia

Site Status

IPS Medicity SAS

Bucaramanga, , Colombia

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Servimed S A S

Bucaramanga, , Colombia

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Preventive Care Ltda

Chía, , Colombia

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Clinica Universitaria Bolivariana

Medellín, , Colombia

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Funcentra

Montería, , Colombia

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Charite - Universitaetsmedizin Berlin (CCM)

Berlin, , Germany

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Medizinische Hochschule Hannover

Hanover, , Germany

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Rheumazentrum Ruhrgebiet

Herne, , Germany

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Rheumatology Unit

Leipzig, , Germany

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Universitaetsmedizin Mainz

Mainz, , Germany

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Szt, Istvan and Szt. Laszlo

Budapest, , Hungary

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Bekes Megyei Pandy Kalman Korhaz

Gyula, , Hungary

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Belvarosi Egeszseghaz Kft. (Leda-Platan Maganklinika es Sebeszeti Kozpont)

Zalaegerszeg, , Hungary

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Chiba University Hospital

Chiba, , Japan

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National Hospital Organization Chiba East Hospital

Chiba, , Japan

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Hospital of the University of Occupational and Enviromental Health

Fukuoka, , Japan

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National Hospital Organization Kyushu Medical Center

Fukuoka, , Japan

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Fukushima Medical University Hospital

Fukushima, , Japan

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Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital

Hiroshima, , Japan

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National Hospital Organization Osaka Minami Medical Center

Kawachi-Nagano, , Japan

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Kawasaki Rheumatism and Internal Medicine Clinic

Kitakyushu, , Japan

Site Status

Toho University Medical Center, Ohashi Hospital

Meguro-ku, , Japan

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Nagasaki University Hospital

Nagasaki, , Japan

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National Hospital Organization Nagoya Medical Center

Nagoya, , Japan

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Kitasato University Hospital

Sagamihara, , Japan

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Sapporo City General Hospital

Sapporo, , Japan

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Hokkaido University Hospital

Sapporo, , Japan

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Sasebo Chuo Hospital

Sasebo, , Japan

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Tohoku University Hospital

Sendai, , Japan

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Keio University Hospital

Shinjuku-ku, , Japan

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Center Hospital of the National Center for Global Health and Medicine

Shinjuku-ku, , Japan

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St. Luke's International Hospital

Tokyo, , Japan

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Juntendo University Hospital

Tokyo, , Japan

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Fujita Health University Hospital

Toyoake, , Japan

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National Hospital Organization Yokohama Medical Center

Yokohama, , Japan

Site Status

Lietuvos sveikatos mokslų universiteto ligoninė Kauno klinik

Kaunas, , Lithuania

Site Status

Klaipeda University Hospital

Klaipėda, , Lithuania

Site Status

Vaiku ligonine Vilniaus Universiteto ligon. Santariskiu fil

Vilnius, , Lithuania

Site Status

Vilnius University Hospital Santariskiu Clinics

Vilnius, , Lithuania

Site Status

Szpital Uniwersytecki nr 2 im dr Jana Biziela w Bydgoszczy

Bydgoszcz, , Poland

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Nzoz Bif Med

Bytom, , Poland

Site Status

Centrum Medyczne AMED oddzial w Lodzi

Lodz, , Poland

Site Status

Samodzielny Publiczny Szpital Kliniczny Nr 4 w Lublinie

Lublin, , Poland

Site Status

Twoja Przychodnia - Centrum Medyczne Nowa Sol

Nowa Sól, , Poland

Site Status

Centrum Medyczne Medens S.C. Grupowa Praktyka Lekarska

Sonoswiec, , Poland

Site Status

Centrum Medyczne Pratia Tychy

Tychy, , Poland

Site Status

Centrum Medyczne Pratia Warszawa

Warsaw, , Poland

Site Status

Reumatika-Centrum Reumatologii, NZOZ

Warsaw, , Poland

Site Status

Uniwersytecki Szpital Kliniczny im. J. Mikulicza-Radeckiego

Wroclaw, , Poland

Site Status

Instituto Portugues de Reumatologia

Lisbon, , Portugal

Site Status

Uls Sao Jose - Hosp. Curry Cabral

Lisbon, , Portugal

Site Status

Hosp. Da Luz Lisboa

Lisbon, , Portugal

Site Status

ULSAM, EPE - Hospital Conde de Bertiandos

Ponte de Lima, , Portugal

Site Status

C.H. de Vila Nova de Gaia/Espinho

Vila Nova de Gaia, , Portugal

Site Status

Regional Clinical Hospital for War Veterans

Kemerovo, , Russia

Site Status

LLL Medical Center Revma-Med

Kemerovo, , Russia

Site Status

Clinical Diagnostic Center 'Ultramed'

Omsk, , Russia

Site Status

Northen-Western State Medical University n.a. I.I. Mechnikov

Saint Petersburg, , Russia

Site Status

Leningrad region clinical hospital

Saint Petersburg, , Russia

Site Status

City Clinical Hospital #31

Saint Petersburg, , Russia

Site Status

Ulyanovsk Regional Clinical Hospital

Ulyanovsk, , Russia

Site Status

Clinical Emergency Hospital n.a. N.V. Solovyev

Yaroslavl, , Russia

Site Status

Institute of Rheumatology Belgrade

Belgrade, , Serbia

Site Status

Institute of Rheumatology

Belgrade, , Serbia

Site Status

Military Medical Academy

Belgrade, , Serbia

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Clinical Hospital Center Bezanijska Kosa

Belgrade, , Serbia

Site Status

University Clinical Center Kragujevac

Kragujevac, , Serbia

Site Status

Institute for Treatment and Rehabilitation Niska Banja

Niška Banja, , Serbia

Site Status

Clinical Center of Vojvodina

Vojvodina, , Serbia

Site Status

Panorama Medical Centre

Cape Town, , South Africa

Site Status

Excellentis Clinical trial Consultants

George, , South Africa

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Clinical Research Unit, University of Pretoria

Pretoria, , South Africa

Site Status

Winelands Medical Research Centre

Stellenbosch, , South Africa

Site Status

Daegu Catholic University Medical Center

Daegu, , South Korea

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Chonbuk National Univ Hospital

Jeonju, , South Korea

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Seoul National University Hospital

Seoul, , South Korea

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Konkuk University Medical Center

Seoul, , South Korea

Site Status

Ajou University Hospital

Suwon, , South Korea

Site Status

Hosp Univ Vall D Hebron

Barcelona, , Spain

Site Status

Hosp. Univ. de Basurto

Bilbao, , Spain

Site Status

Hosp Reina Sofia

Córdoba, , Spain

Site Status

Hosp. Clinico San Carlos

Madrid, , Spain

Site Status

Hosp. Univ. 12 de Octubre

Madrid, , Spain

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Hosp Regional Univ de Malaga

Málaga, , Spain

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Hosp. Univ. Infanta Sofia

San Sebastián de los Reyes, , Spain

Site Status

Hosp. Infanta Luisa

Seville, , Spain

Site Status

Hosp. Do Meixoeiro

Vigo -Pontevedra, , Spain

Site Status

Kaohsiung Medical University Chung Ho Memorial Hospital

Kaohsiung City, , Taiwan

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Chang Gung Memorial Hospital

Kwei-san Hsiang, , Taiwan

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Chung Shan Medical University Hospital

Taichung, , Taiwan

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China Medical University Hospital

Taichung, , Taiwan

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National Taiwan University Hospital

Taipei, , Taiwan

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Cathay General Hospital

Taipei, , Taiwan

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Taipei Medical University

Taipei, , Taiwan

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Taipei Veterans General Hospital

Taipei, , Taiwan

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Phramongkutklao Hospital and Medical College

Bangkok, , Thailand

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Rajavhiti Hospital

Bangkok, , Thailand

Site Status

Ramathibodi Hospital

Bangkok, , Thailand

Site Status

Siriraj Hospital

Bangkok, , Thailand

Site Status

Songklanagarind hospital

Hat Yai, , Thailand

Site Status

Chiang Mai University

Muang, , Thailand

Site Status

Mechnikov Inst, Miska bagatoprofilna likarnia #18

Kharkiv, , Ukraine

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Kyiv City Clinical Hospital #3

Kyiv, , Ukraine

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Kyivska oblasna klinichna likarnia

Kyiv, , Ukraine

Site Status

Odeska oblasna klinichna likarnia

Odesa, , Ukraine

Site Status

Multidisciplinary Medical Center of Odessa National Medical University

Odesa, , Ukraine

Site Status

MNPE 'Vinnytsia Regional Clinical Hospital named after M.I. Pyrogov of Vinnytsia Regional Council'

Vinnytsia, , Ukraine

Site Status

Naukovo-doslidnyi inst. Reabilit. Pyrogova [Revmatologichne]

Vinnytsia, , Ukraine

Site Status

Countries

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United States Argentina Bulgaria Canada China Colombia Germany Hungary Japan Lithuania Poland Portugal Russia Serbia South Africa South Korea Spain Taiwan Thailand Ukraine

References

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van Vollenhoven RF, Kalunian KC, Dorner T, Hahn BH, Tanaka Y, Gordon RM, Shu C, Fei K, Gao S, Seridi L, Gallagher P, Lo KH, Berry P, Zuraw QC. Phase 3, multicentre, randomised, placebo-controlled study evaluating the efficacy and safety of ustekinumab in patients with systemic lupus erythematosus. Ann Rheum Dis. 2022 Oct 12;81(11):1556-1563. doi: 10.1136/ard-2022-222858.

Reference Type DERIVED
PMID: 35798534 (View on PubMed)

Hannon CW, McCourt C, Lima HC, Chen S, Bennett C. Interventions for cutaneous disease in systemic lupus erythematosus. Cochrane Database Syst Rev. 2021 Mar 9;3(3):CD007478. doi: 10.1002/14651858.CD007478.pub2.

Reference Type DERIVED
PMID: 33687069 (View on PubMed)

Provided Documents

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Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

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2017-001489-53

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

CNTO1275SLE3001

Identifier Type: OTHER

Identifier Source: secondary_id

CR108440

Identifier Type: -

Identifier Source: org_study_id

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