- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: Plasmapheresis.
Displaying page 1 of 2.
EudraCT Number: 2022-000641-33 | Sponsor Protocol Number: PAX | Start Date*: 2022-04-21 | |||||||||||
Sponsor Name:Fundació FLS de Lluita contra la Sida, les Malalties Infeccioses i la Promoció de la Salut i La Ciència | |||||||||||||
Full Title: Plasma Exchange Therapy for Post- COVID-19 Condition: A Pilot, Randomized Double-Blind Study | |||||||||||||
Medical condition: Post-Acute-Covid-19 Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002817-37 | Sponsor Protocol Number: PIX200701 | Start Date*: 2008-07-29 | |||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO "CARLO BESTA" | |||||||||||||
Full Title: A PHASE II, PLACEBO CONTROLLED, DOSE FINDING PILOT STUDY OF PIXANTRONE EFFICACY ADMINISTERED INTRAVENOUSLY IN PATIENTS AFFECTED WITH MYASTHENIA GRAVIS | |||||||||||||
Medical condition: Patients affected with MG showing clinically meaningful improvement after therapeutic plasmapheresis. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001995-71 | Sponsor Protocol Number: PLATIG-1404 | Start Date*: 2014-07-03 |
Sponsor Name:Plazmaferezis Állomás Közhasznú Nonprofit Kft | ||
Full Title: Open label multicenter prospective trial to assess the tetanus titer in subject of regular plasmapharesis | ||
Medical condition: healthy subjects eligible for tetanus booster vaccination | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002711-94 | Sponsor Protocol Number: HO124WM | Start Date*: 2014-09-19 | ||||||||||||||||
Sponsor Name:HOVON Foundation | ||||||||||||||||||
Full Title: HOVON 124 WM study: A prospective phase I/II trial of the combination of ixazomib citrate, rituximab and dexamethasone in patients with relapsed or progressive Waldenström's macroglobulinemia. | ||||||||||||||||||
Medical condition: Waldenström's macroglobulinemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) BE (Ongoing) GR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000726-11 | Sponsor Protocol Number: SHP616-302 | Start Date*: 2016-03-08 | |||||||||||
Sponsor Name:Shire Viropharma, Inc. | |||||||||||||
Full Title: A randomized double-blind placebo-controlled study to evaluate the efficacy and safety of Cinryze® (C1 esterase inhibitor [human]) for the treatment of acute antibody-mediated rejection in kidney t... | |||||||||||||
Medical condition: Acute Antibody Mediated Rejection (AMR) in kidney transplant patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001598-25 | Sponsor Protocol Number: IG1002 | Start Date*: 2011-10-25 | |||||||||||
Sponsor Name:INSTITUTO GRIFOLS, S.A. | |||||||||||||
Full Title: A multicenter, randomized, controlled study to evaluate the efficacy and safety of short-term plasma exchange followed by long-term plasmaphereses with infusion of human albumin combined with intra... | |||||||||||||
Medical condition: Mild to Moderate Alzheimer's Disease patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007019-33 | Sponsor Protocol Number: RES.I.ST. EXPERIENCED | Start Date*: 2008-12-24 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO EMOFILIA E TROMBOSI ANGELO BIANCHI BONOMI | |||||||||||||
Full Title: IMMUNE TOLERANCE INDUCTION STUDY IN PATIENTS WITH SEVERE TYPE A HAEMOPHILIA WITH INHIBITOR AFTER FAILURE OF A PREVIOUS INDUCTION OF IMMUNE TOLERANCE WITH FVIII CONCENTRATES WITHOUT VON WILLEBRAND F... | |||||||||||||
Medical condition: SEVERE TYPE A HAEMOPHILIA | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) ES (Prematurely Ended) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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: 2008-008285-12 | Sponsor Protocol Number: 1655/08 | Start Date*: 2009-10-14 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: PROSPECTIVE STUDY IBDISC: Regeneration and Immunity in patients affected by IBD undergoing immunomodulatory treatment and adjuvant role of G-CSF and/or plasmapheresis (Inflammatory Bowel Disease... | ||||||||||||||||||
Medical condition: Inflammatory bowel disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004998-53 | Sponsor Protocol Number: OMB116024 | Start Date*: 2013-02-05 |
Sponsor Name:National and Kapodistrian University of Athens | ||
Full Title: A phase II study of the efficacy of the combination of ofatumumab with fludarabine and cyclophosphamide in patients with relapsed or refractory Waldenström’s Macroglobulinemia. | ||
Medical condition: Relapsed or refractory Waldenström’s Macroglobulinemia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000441-12 | Sponsor Protocol Number: 0624-201 | Start Date*: 2012-09-21 | |||||||||||
Sponsor Name:VIROPHARMA Incorporated | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled pilot study to evaluate the safety and effect of Cinryze (C1 Esterase Inhibitor (Human)) for the treatment of acute antibody-mediated rejection in rec... | |||||||||||||
Medical condition: Acute Antibody Mediated Rejection (AMR) in kidney transplant patients | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003022-32 | Sponsor Protocol Number: CL012_140 | Start Date*: 2019-10-12 | |||||||||||
Sponsor Name:ChemoCentryx, Inc. | |||||||||||||
Full Title: An Open Label, Intra-Subject Dose Escalation Study of CCX140-B in Subjects with Primary Focal Segmental Glomerulosclerosis (FSGS) and Nephrotic Syndrome | |||||||||||||
Medical condition: Primary Focal Segmental Glomerulosclerosis (FSGS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001936-86 | Sponsor Protocol Number: COMET | Start Date*: 2020-10-19 | |||||||||||
Sponsor Name:Hannover Medical School | |||||||||||||
Full Title: A prospective, randomized, open label Phase 2 clinical trial to evaluate superiority of anti-SARS-CoV-2 convalescent plasma versus standard-of-care in hospitalized patients with mild COVID-19 | |||||||||||||
Medical condition: Hospitalized patients with mild SARS-CoV-2 infection (WHO R&D Blueprint Ordinal Scale for Clinical Improvement = 3 or 4) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006060-89 | Sponsor Protocol Number: NMSG29/21 | Start Date*: 2021-03-26 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: Selinexor with alternating bortezomib or lenalidomide plus dexamethasone in transplant ineligible newly diagnosed multiple myeloma patients (SABLe): An Investigator Sponsored Trial | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Ongoing) NO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003563-31 | Sponsor Protocol Number: 26866138CAN 2021 | Start Date*: 2007-03-09 | |||||||||||
Sponsor Name:European Myeloma Network | |||||||||||||
Full Title: Phase II Study of Combination Bortezomib (VELCADE, PS-341), Dexamethasone, and Rituximab (MabThera) (BDR) in Patients with previously untreated Waldenstrom’s Macroglobulinemia (WM). | |||||||||||||
Medical condition: Newly diagnosed Waldenstrom's macroglobulinemia (WM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Ongoing) NL (Ongoing) ES (Ongoing) FR (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005732-29 | Sponsor Protocol Number: MOM-M281-011 | Start Date*: 2021-11-19 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Nipocalimab Administered to Adults with Generali... | |||||||||||||
Medical condition: Myasthenia gravis (MG). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) PL (Trial now transitioned) SE (Trial now transitioned) DK (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003627-30 | Sponsor Protocol Number: 20170367744 | Start Date*: 2018-06-27 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Odense Research Center for Anaphylaxis (ORCA) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Protection from food induced anaphylaxis by reducing serum level of specific IgE | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Food Allergy with Anaphylaxis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000007-28 | Sponsor Protocol Number: DSMMXII | Start Date*: 2009-05-22 | |||||||||||
Sponsor Name:Universitaetsklinikum Wuerzburg | |||||||||||||
Full Title: Lenalidomide (Revlimid®), Adriamycin and Dexamethasone (RAD) as an Induction Therapy in Newly Diagnosed Multiple Myeloma Followed by a Risk-Defined Transplant Strategy and Lenalidomide Maintenance ... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016616-21 | Sponsor Protocol Number: DSMMXIV | Start Date*: 2011-10-20 | |||||||||||
Sponsor Name:Wuerzburg University Hospital | |||||||||||||
Full Title: Lenalidomide, Adriamycin, Dexamethasone (RAD) Versus Lenalidomide, Bortezomib, Dexamethasone (VRD) for Induction in Newly Diagnosed Multiple Myeloma followed by Response-adapted Consolidation and ... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007016-15 | Sponsor Protocol Number: RES.I.ST. NAÏVE | Start Date*: 2008-12-24 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO EMOFILIA E TROMBOSI ANGELO BIANCHI BONOMI | |||||||||||||
Full Title: RANDOMISED STUDY OF FIRST CHOICE IMMUNOTOLERANCE INDUCTION IN PATIENTS WITH SEVERE TYPE A HAEMOPHILIA WITH INHIBITOR AT HIGH RISK OF FAILURE: COMPARISON OF INDUCTION OF IMMUNE TOLERANCE WITH FVIII ... | |||||||||||||
Medical condition: SEVERE TYPE A HAEMOPHILIA | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) ES (Ongoing) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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