- Trials with a EudraCT protocol (136)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
136 result(s) found for: Glomerulonephritis.
Displaying page 2 of 7.
| EudraCT Number: 2020-001537-13 | Sponsor Protocol Number: ALXN1210-NEPH-202 | Start Date*: 2021-03-25 | ||||||||||||||||
| Sponsor Name:Alexion Pharmaceuticals, Inc. | ||||||||||||||||||
| Full Title: A Phase 2, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Ravulizumab in Adult Participants With Proliferative Lupus Nephritis (LN) or Immunoglobulin A Ne... | ||||||||||||||||||
| Medical condition: Lupus Nephritis (LN) Immunoglobulin A Nephropathy (IgAN) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) SE (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-005526-17 | Sponsor Protocol Number: 417-201-00012 | Start Date*: 2022-12-09 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development and Commercialization, Inc. | |||||||||||||
| Full Title: A Phase 2/3, Multicenter, Open-label Trial to Evaluate the Long-term Safety, Tolerability, and Efficacy of Sibeprenlimab Administered Subcutaneously in Subjects with Immunoglobulin A Nephropathy | |||||||||||||
| Medical condition: Immunoglobulin A Nephropathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-002345-64 | Sponsor Protocol Number: 181501 | Start Date*: 2015-11-12 | |||||||||||
| Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
| Full Title: A Phase 2 Study to Assess the Efficacy and Safety of Intravenous Infusion with Human Soluble Recombinant Fc-gamma Receptor IIB (SM101/BAX 1810) in Subjects with Immunoglobulin A Nephropathy (IgAN) | |||||||||||||
| Medical condition: IgA Nephropathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-018189-36 | Sponsor Protocol Number: 0908143 | Start Date*: 2010-05-17 | ||||||||||||||||
| Sponsor Name:CHU Saint-Etienne | ||||||||||||||||||
| Full Title: Prévention chez le receveur avec néphropathie à IgA primaire (NIGA) de la Récidive Après Transplantation rénale: ATG-F versus Basiliximab, comme traitements immunosuppresseurs d’induction. Etude ... | ||||||||||||||||||
| Medical condition: IgA glomerulonephritis and first transplant | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) ES (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-001365-26 | Sponsor Protocol Number: AN-IGN3321 | Start Date*: 2014-08-21 | |||||||||||
| Sponsor Name:Anthera Pharmaceuticals, Inc | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Phase 2/3 Study to Evaluate the Efficacy and Safety of Blisibimod Administration in Subjects with IgA Nephropathy | |||||||||||||
| Medical condition: IgA Nephropathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) DE (Completed) IT (Prematurely Ended) HU (Completed) ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004892-41 | Sponsor Protocol Number: VT-001-0050 | Start Date*: 2021-07-13 | |||||||||||
| Sponsor Name:Vera Therapeutics, Inc. | |||||||||||||
| Full Title: A Phase IIb Randomized, Double-Blinded, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy and Safety of Atacicept in Subjects with IgA Nephropathy (IgAN) | |||||||||||||
| Medical condition: IgA Nephropathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) CZ (Trial now transitioned) DE (Trial now transitioned) GR (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-000226-55 | Sponsor Protocol Number: STARMEN01-2013 | Start Date*: 2014-04-16 | |||||||||||
| Sponsor Name:Fundacion Renal Iñigo Alvarez Toledo | |||||||||||||
| Full Title: European Multicenter and Open-Label Controlled Randomized Trial to evaluate the Efficacy of Sequential Treatment with Tacrolimus-Rituximab versus Steroids plus Cyclophosphamide in patientes with Pr... | |||||||||||||
| Medical condition: Primary membranous nephropathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000385-38 | Sponsor Protocol Number: BEL116472 | Start Date*: 2012-05-18 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
| Full Title: BEL116472. A 2 year mechanistic study of belimumab in Idiopathic Membranous Glomerulonephropathy | |||||||||||||
| Medical condition: Idiopathic Membranous Glomerulonephropathy (IMGN) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003233-38 | Sponsor Protocol Number: WA41937 | Start Date*: 2021-03-02 | |||||||||||
| Sponsor Name:F.Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A PHASE III, RANDOMIZED, OPEN-LABEL ACTIVE COMPARATOR-CONTROLLED MULTICENTER STUDY TO EVALUATE EFFICACY AND SAFETY OF OBINUTUZUMAB IN PATIENTS WITH PRIMARY MEMBRANOUS NEPHROPATHY | |||||||||||||
| Medical condition: Primary Membranous Nephropathy (pMN) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003402-33 | Sponsor Protocol Number: CL005_168 | Start Date*: 2015-02-09 | |||||||||||
| Sponsor Name:ChemoCentryx, Inc. | |||||||||||||
| Full Title: An open-label phase 2 study to evaluate the safety and efficacy of CCX168 in subjects with IgA Nephropathy on stable RAAS blockade. | |||||||||||||
| Medical condition: IgAN is reported as the most common glomerulonephritis worldwide. It is associated with a wide spectrum of disease severity and rate of progression of renal failure. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001923-11 | Sponsor Protocol Number: Nef-202 | Start Date*: 2012-10-17 | |||||||||||
| Sponsor Name:Pharmalink AB | |||||||||||||
| Full Title: A Multicentre, Interventional Treatment, Randomised, Double-Blind, Single Group Assignment, Placebo Controlled Study to Evaluate the Efficacy and Safety of Two Different Doses of Nefecon® in Primar... | |||||||||||||
| Medical condition: Primary IgA nephropathy patients at risk of developing end stage renal disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) CZ (Completed) DE (Completed) BE (Completed) SE (Completed) DK (Completed) IT (Completed) GB (Completed) NL (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003308-14 | Sponsor Protocol Number: Nef-301OLE | Start Date*: 2020-10-21 | |||||||||||
| Sponsor Name:Calliditas Therapeutics AB | |||||||||||||
| Full Title: An Open-Label Extension (OLE) Study to Evaluate the Efficacy and Safety of Nefecon Treatment in Patients With IgA Nephropathy Who Have Completed Study Nef-301 | |||||||||||||
| Medical condition: Primary IgA nephropathy patients at risk of developing end stage renal disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) SE (Completed) PL (Completed) BE (Completed) FR (Completed) GB (GB - no longer in EU/EEA) GR (Completed) FI (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001426-22 | Sponsor Protocol Number: ALXN2050-NEPH-201 | Start Date*: 2022-05-30 | ||||||||||||||||
| Sponsor Name:Alexion Pharmaceuticals, Inc. | ||||||||||||||||||
| Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled, Dose-finding Study to Evaluate the Efficacy and Safety of ALXN2050 in Adult Participants with Proliferative Lupus Nephritis (LN) or Immunogl... | ||||||||||||||||||
| Medical condition: Lupus Nephritis (LN) Immunoglobulin A Nephropathy (IgAN) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-002262-31 | Sponsor Protocol Number: MS700461-0035 | Start Date*: 2017-03-17 | ||||||||||||||||
| Sponsor Name:Merck KGaA | ||||||||||||||||||
| Full Title: A Phase II Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Atacicept in IgA Nephropathy | ||||||||||||||||||
| Medical condition: IgA Nephropathy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-005054-19 | Sponsor Protocol Number: MOR202C206 | Start Date*: 2021-07-28 | |||||||||||
| Sponsor Name:Human Immunology Biosciences, Inc | |||||||||||||
| Full Title: A Double Blind, Randomized, Placebo-Controlled, Multicenter Phase IIa, Clinical Trial to Assess Efficacy and Safety of the Human Anti-CD38 Antibody Felzartamab in IgA Nephropathy - IGNAZ | |||||||||||||
| Medical condition: IgA Nephropathy (IgAN) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) BG (Completed) DE (Completed) BE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004902-16 | Sponsor Protocol Number: Nef-301 | Start Date*: 2018-06-04 | |||||||||||
| Sponsor Name:Calliditas Therapeutics AB | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo Controlled Study to Evaluate Efficacy and Safety of Nefecon in Patients with Primary IgA Nephropathy at Risk of Progressing to End-Stage Renal Disease (NefIgArd). | |||||||||||||
| Medical condition: Primary IgA nephropathy patients at risk of developing end stage renal disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) SE (Completed) BE (Completed) FI (Completed) ES (Completed) GB (GB - no longer in EU/EEA) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000075-33 | Sponsor Protocol Number: OMS721-IGA-001 | Start Date*: 2018-06-07 |
| Sponsor Name:Omeros Corporation | ||
| Full Title: A Randomized, Double-blind, Placebo-controlled, Phase 3 Study of the Safety and Efficacy of OMS721 in Patients with Immunoglobulin A (IgA) Nephropathy (ARTEMIS – IGAN) | ||
| Medical condition: IgA nephropathy (IgAN) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) LT (Prematurely Ended) SE (Completed) ES (Prematurely Ended) BE (Completed) AT (Prematurely Ended) PL (Prematurely Ended) BG (Completed) GB (GB - no longer in EU/EEA) DE (Completed) IT (Prematurely Ended) GR (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-003767-25 | Sponsor Protocol Number: APL2-C3G-310 | Start Date*: 2022-03-08 | |||||||||||||||||||||
| Sponsor Name:Apellis Pharmaceuticals, Inc. | |||||||||||||||||||||||
| Full Title: A Phase 3, Randomized, Placebo-Controlled, Double-Blinded, Multicenter Study to Evaluate the Efficacy and Safety of Pegcetacoplan in Patients with C3 Glomerulopathy or Immune-Complex Membranoprolif... | |||||||||||||||||||||||
| Medical condition: complement 3 glomerulopathy (C3G)/immune complex membranoproliferative glomerulonephritis (IC-MPGN) | |||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) CZ (Completed) BE (Completed) AT (Trial now transitioned) FR (Completed) PL (Completed) IT (Trial now transitioned) ES (Ongoing) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2011-000242-38 | Sponsor Protocol Number: BEL114674 | Start Date*: 2013-01-09 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: BEL114674: A 2 year study of efficacy and safety of intravenous belimumab versus placebo in subjects with idiopathic membranous nephropathy | |||||||||||||
| Medical condition: Idiopathic Membranous Nephropathy (IMN) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) CZ (Prematurely Ended) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-007793-29 | Sponsor Protocol Number: IGG-SN-DEPOMED | Start Date*: 2008-02-11 | |||||||||||
| Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
| Full Title: Efficacy of long acting steroids intramuscular therapy in nephrotic syndrome: pilot study. | |||||||||||||
| Medical condition: NEPHROSIC SYNDROME | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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