- Trials with a EudraCT protocol (64)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
64 result(s) found for: Lupus Nephritis.
Displaying page 1 of 4.
EudraCT Number: 2021-006544-26 | Sponsor Protocol Number: INTONATE | Start Date*: 2022-12-23 | ||||||||||||||||
Sponsor Name:A.S.L. TO 2 | ||||||||||||||||||
Full Title: INTONATE INtensified procol for lupus nephritis with riTuximab and nO maintaiNAnce ThErapy | ||||||||||||||||||
Medical condition: lupus nephritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004047-86 | Sponsor Protocol Number: AIS-A03 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Alpine Immune Sciences, Inc. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF ALPN-101 IN SYSTEMIC LUPUS ERYTHEMATOSUS | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Systemic lupus erythematosus (SLE) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) PL (Completed) ES (Prematurely Ended) HU (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020968-38 | Sponsor Protocol Number: CNTO136LUN2001 | Start Date*: 2011-03-17 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Proof-of-Concept Study to Evaluate Efficacy and Safety of Treatment with CNTO 136 Administered Intravenously in Subjects with Active Lup... | |||||||||||||
Medical condition: Active Lupus Nephritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000594-69 | Sponsor Protocol Number: 211LE202 | Start Date*: 2014-06-20 | |||||||||||
Sponsor Name:Biogen Idec Research Limited | |||||||||||||
Full Title: A Dose-Blinded, 2-Dose Level, Parallel-Group, Multicenter, Long-Term Extension Study to Evaluate the Long-Term Safety, Efficacy, and Immunogenicity of BIIB023 in Subjects with Lupus Nephritis | |||||||||||||
Medical condition: Lupus Nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) HU (Completed) PL (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005772-19 | Sponsor Protocol Number: CAIN457Q12301E1 | Start Date*: 2022-07-12 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A three-year, open-label extension study of subcutaneous secukinumab to evaluate the long-term efficacy, safety and tolerability in patients with active lupus nephritis | |||||||||||||
Medical condition: Lupus Nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Prematurely Ended) PT (Prematurely Ended) SK (Completed) GR (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018329-20 | Sponsor Protocol Number: LN-LAQ-201 | Start Date*: 2010-05-07 | |||||||||||
Sponsor Name:Teva Pharmaceutical Industries Ltd. | |||||||||||||
Full Title: A Phase IIa, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Study to Evaluate the Safety, Tolerability and Clinical Effect of Laquinimod in Active Lupus Nephritis Patients, in Combinati... | |||||||||||||
Medical condition: Active Lupus Nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000243-80 | Sponsor Protocol Number: MSV_LE | Start Date*: 2022-05-26 | |||||||||||
Sponsor Name:Hospital Universitario Rio Hortega | |||||||||||||
Full Title: PHASE II, DOUBLE-BLIND, PLACEBO-CONTROLLED CLINICAL TRIAL TO EVALUATE SAFETY AND EFFICACY OF MESENCHYMAL CELLS (MSV-allo®) IN THE TREATMENT OF LUPUS NEPHRITIS. | |||||||||||||
Medical condition: Lupus nephritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003201-34 | Sponsor Protocol Number: U2970g | Start Date*: 2016-08-07 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche AG | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Rituximab in Subjects With ISN/RPS Class III or IV Lupus Nephritis | |||||||||||||
Medical condition: ISN/RPS 2003 Class III or IV Lupus Nephritis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004518-15 | Sponsor Protocol Number: 28113 | Start Date*: 2008-08-05 | |||||||||||
Sponsor Name:Merck Serono International | |||||||||||||
Full Title: A Phase 2/3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Atacicept in Subjects with Lupus Nephritis in Combination with Mycophenolate Mofetil Therapy | |||||||||||||
Medical condition: Lupus nephritis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002179-34 | Sponsor Protocol Number: SLE01_ENK | Start Date*: 2005-08-10 | |||||||||||
Sponsor Name:Euro Nippon Kayaku GmbH | |||||||||||||
Full Title: SAFETY AND EFFICACY STUDY ON DEOXYSPERGUALIN (NKT-01) IN PATIENTS WITH UNCONTROLLED LUPUS NEPHRITIS RECEIVING ORAL CORTICOSTEROIDS AND PRIOR TREATMENT OF STANDARD IMMUNOSUPPRESSIVE THERAPY - a pros... | |||||||||||||
Medical condition: Systemic lupus erythrematosus (SLE) is an aggressive autoimmune disease. The chronic inflammatory processes involve many organs like the skin, lung, kidneys, central and peripheral nervous system, ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003155-38 | Sponsor Protocol Number: CNTO1959LUN2001 | Start Date*: 2020-08-09 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study of Guselkumab in Subjects with Active Lupus Nephritis | |||||||||||||
Medical condition: Active Lupus Nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005568-79 | Sponsor Protocol Number: 80202135LUN2001 | Start Date*: 2021-11-08 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled Study of Nipocalimab in Adult Participants with Active Lupus Nephritis | |||||||||||||
Medical condition: Active Lupus Nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001619-35 | Sponsor Protocol Number: P1200_41 | Start Date*: 2017-06-01 | |||||||||||
Sponsor Name:Cliniques Universitaires Saint-lus, Université catholique de Louvain | |||||||||||||
Full Title: Exploratory pathophysiological study in five patients suffering from new-onset lupus nephritis and treated with rituximab as first-line treatment | |||||||||||||
Medical condition: Lupus Nephritis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001442-29 | Sponsor Protocol Number: D3461C00007 | Start Date*: 2016-01-14 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multicentre, Randomised, Double-blind, Placebo-controlled, Phase 2 Study Evaluating the Efficacy and Safety of Anifrolumab in Adult Subjects with Active Proliferative Lupus Nephritis | |||||||||||||
Medical condition: Lupus Nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) DE (Completed) ES (Completed) GB (GB - no longer in EU/EEA) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002159-32 | Sponsor Protocol Number: 211LE201 | Start Date*: 2012-03-30 | |||||||||||
Sponsor Name:Biogen Idec Research Limited | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of BIIB023 in Subjects With Lupus Nephritis | |||||||||||||
Medical condition: Lupus Nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Prematurely Ended) BE (Completed) DE (Completed) ES (Prematurely Ended) HU (Completed) IT (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005856-32 | Sponsor Protocol Number: RITULUP | Start Date*: 2012-05-21 | |||||||||||
Sponsor Name:Fundación Progreso y Salud | |||||||||||||
Full Title: Comparison of the efficacy of two rituximab treatment regimens in patients with lupus nephropathy resistant to conventional treatment | |||||||||||||
Medical condition: Long-term relapse after treatment of lupus nephritis (LN) resistant to conventional treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002221-36 | Sponsor Protocol Number: 28779 | Start Date*: 2008-10-17 | |||||||||||
Sponsor Name:Merck Serono International, An affiliate of Merck KGaA, Darmstadt, Germany | |||||||||||||
Full Title: A Phase II/III, randomized, double-blind, placebo-controlled trial to evaluate the safety and efficacy of atacicept in combination with corticosteroids and sequential therapy with cyclophosphamide ... | |||||||||||||
Medical condition: Lupus Nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004917-41 | Sponsor Protocol Number: WX17801 | Start Date*: 2005-09-05 | |||||||||||
Sponsor Name:Aspreva International Ltd. | |||||||||||||
Full Title: A prospective, randomized, active controlled, parallel group, multi-center trial to assess the efficacy and safety of mycophenolate mofetil (MMF) in inducing response and maintaining remission in s... | |||||||||||||
Medical condition: Lupus Nephritis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) CZ (Completed) ES (Completed) BE (Completed) PT (Completed) AT (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003230-93 | Sponsor Protocol Number: CCFZ533X2202 | Start Date*: 2018-05-09 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, placebo-controlled, patient and investigator blinded study investigating the safety, tolerability, pharmacokinetics and preliminary efficacy of multiple doses of CFZ533 in patients wi... | |||||||||||||
Medical condition: Lupus Nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004852-62 | Sponsor Protocol Number: FARM7KWBZ4 | Start Date*: 2009-02-09 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA DELLA SECONDA UNIVERSITA` DEGLI STUDI DI NAPOLI | ||||||||||||||||||
Full Title: Safety and clinical efficacy of abetimus sodium (LJP-394) in prevention of renal flares in patients with systemic lupus erythematosus and a history of renal disease. | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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