- Trials with a EudraCT protocol (44)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
44 result(s) found for: Idiopathic thrombocytopenic purpura.
Displaying page 1 of 3.
EudraCT Number: 2004-000172-13 | Sponsor Protocol Number: 20030213 | Start Date*: 2008-08-20 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: An Open Label Study Evaluating the Safety and Efficacy of Long-Term Dosing of AMG 531 in Thrombocytopenic Subjects with Immune (Idiopathic) Thrombocytopenic Purpura ( ITP) | |||||||||||||
Medical condition: Thrombocytopenia in subjects with Immune Thrombocytopenic Purpura (ITP) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BE (Completed) AT (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000859-15 | Sponsor Protocol Number: ML 18542 | Start Date*: 2005-04-14 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Randomized prospective study comparing dexamethasone and dexamethasone plus rituximab in the treatment of idiopathic thrombocytopenic purpura (ITP) in adults. | |||||||||||||
Medical condition: Front-line treatment of adult ITP | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000638-37 | Sponsor Protocol Number: 20040209 | Start Date*: 2008-02-28 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: An Open Label Study of Romiplostim in Adult Thrombocytopenic Subjects with Immune (Idiopathic) Thrombocytopenic Purpura (ITP) | |||||||||||||
Medical condition: Immune (Idiopathic) Thrombocytopenic Purpura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) CZ (Completed) BE (Completed) AT (Completed) IE (Completed) GB (Completed) IT (Completed) ES (Prematurely Ended) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003552-35 | Sponsor Protocol Number: GAM10-02 | Start Date*: 2006-03-28 | |||||||||||
Sponsor Name:Octapharma AG | |||||||||||||
Full Title: Clinical study to evaluate the efficacy and safety of Octagam® 10% in Idiopathic Thrombocytopenic Purpura in adults. | |||||||||||||
Medical condition: Idiopathic thrombocytopenic purpura, in adults actively bleeding or at high risk bleeding. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) CZ (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019987-35 | Sponsor Protocol Number: 20080435 | Start Date*: 2010-07-23 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Phase 2, Interventional, Single Arm Study Describing Platelet Responses and ITP Remission Rates in Adult Subjects with Immune Thrombocytopenia Purpura Receiving Romiplostim. | |||||||||||||
Medical condition: Adult immune thrombocytopenic purpura (ITP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) GB (Completed) ES (Completed) FR (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000263-27 | Sponsor Protocol Number: IgPro10_4001 | Start Date*: 2011-07-22 | |||||||||||
Sponsor Name:CSL Behring LLC | |||||||||||||
Full Title: An open-label, prospective, multicenter study to investigate the specificity of in vivo antibody binding to red blood cells in subjects with chronic immune thrombocytopenic purpura (ITP) treated wi... | |||||||||||||
Medical condition: Chronic immune thrombocytopenic purpura (ITP) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000537-11 | Sponsor Protocol Number: ZLB03_003CR | Start Date*: 2004-12-01 |
Sponsor Name:ZLB Behring AG | ||
Full Title: An open-label, multicenter study on the efficacy and safety of IgPro10 in patients with chronic immune thrombocytopenic purpura (ITP) | ||
Medical condition: Immune thrombocytopenic purpura (ITP) is the most common autoimmune disease. It is a bleeding disorder characterized by decreased counts of circulating platelets and normal or increased numbers of ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000417-30 | Sponsor Protocol Number: GIMEMA ITP0207 | Start Date*: 2008-06-19 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL'ADULTO | |||||||||||||
Full Title: Randomized study for the treatment of primary Immune Thrombocytopenic Purpura (ITP) in newly diagnosed untreated adult patients. Comparison of standard dose prednisone versus high-dose Dexamethas... | |||||||||||||
Medical condition: ITP Primary Immune Thrombocytopenic Purpura in newly diagnosed untreated adult patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003569-42 | Sponsor Protocol Number: 20060195 | Start Date*: 2007-09-29 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: Estudio Aleatorizado, Doble Ciego, Controlado con Placebo, de Fase 1/2 para Determinar la Seguridad y la Eficacia de AMG 531 en Sujetos Pediátricos Trombocitopénicos con Púrpura Trombocitopénica I... | |||||||||||||
Medical condition: Púrpura Trombocitopénica Inmune (Idiopática) (PTI) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010421-39 | Sponsor Protocol Number: TRA112940 | Start Date*: 2010-03-10 | |||||||||||
Sponsor Name:GlaxoSmithKline | |||||||||||||
Full Title: A longitudinal 2-year bone marrow study of eltrombopag olamine (SB-497115-GR) in previously treated adults, with chronic immune (idiopathic) thrombocytopenic purpura (ITP). | |||||||||||||
Medical condition: Chronic Idiopathic Thrombocytopenic Purpura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) FR (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001597-33 | Sponsor Protocol Number: 20081203 | Start Date*: 2009-06-18 | |||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||
Full Title: Development of chronic disease in newly diagnosed Idiopathic Thrombocytopenic Purpura of Childhood. A randomized controlled study on the influence of treatment with intravenous gammaglobulin on the... | |||||||||||||
Medical condition: Acute Idiopathic Thrombocytopenic Purpura (ITP) in children | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003700-18 | Sponsor Protocol Number: 20060131 | Start Date*: 2007-02-05 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Randomized, Controlled, Open- label Study Evaluating the Efficacy and Tolerability of AMG 531 versus Medical Standard of Care as Chronic Therapy for Non-splenectomized Subjects with Immune (Idiop... | |||||||||||||
Medical condition: Immune (idiopathic) thrombocytopenic purpura (ITP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) GB (Completed) FR (Completed) PT (Completed) CZ (Completed) BE (Completed) DE (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000796-16 | Sponsor Protocol Number: GAMr-30 | Start Date*: 2012-07-09 | |||||||||||
Sponsor Name:OCTAPHARMA AG | |||||||||||||
Full Title: PROSPECTIVE, OPEN-LABEL, NON-CONTROLLED, MULTICENTER, PHASE III CLINICAL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF OCTAGAM 10% IN PRIMARY IMMUNE THROMBOCYTOPENIA | |||||||||||||
Medical condition: Primary Immune Thrombocytopenia (ITP) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004295-22 | Sponsor Protocol Number: NL59645.098.16 | Start Date*: 2017-04-10 | |||||||||||
Sponsor Name:Hagaziekenhuis | |||||||||||||
Full Title: Treatment of thromBocytopenia with EltRombopag or Intravenous Immune Globulin (IVIG) Before and DurING Invasive Procedures in Patients with Immune ThrombocytoPenia. | |||||||||||||
Medical condition: Immune thrombocytopenia patients with low platelets and in need of surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001354-29 | Sponsor Protocol Number: I10E-0719 | Start Date*: 2011-10-12 | |||||||||||
Sponsor Name:LFB BIOTECHNOLOGIES | |||||||||||||
Full Title: An open-label, multicentre efficacy and safety study of I10E in patients with primary Immune ThrombocytoPenia (ITP) | |||||||||||||
Medical condition: ITP diagnosis being defined by ASH-2011 and BCSH 2010 criteria adopting the new consensus terminology proposed by an international working group (Rodeghiero et al, 2009) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2009-014589-24 | Sponsor Protocol Number: NGAM-02 | Start Date*: 2011-09-22 | |||||||||||
Sponsor Name:Octapharma AG | |||||||||||||
Full Title: Prospective, Open-label, Non-controlled, Multicenter, Phase III Clinical Study to Evaluate the Efficacy and Safety of Immunoglobulin Intravenous (Human) 10% (NEWGAM) in Primary Immune Thrombocytopenia | |||||||||||||
Medical condition: Primary Immune Thrombocytopenia (ITP) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) CZ (Prematurely Ended) BG (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002943-10 | Sponsor Protocol Number: TRA108057 | Start Date*: 2007-04-19 | |||||||||||
Sponsor Name:GlaxoSmithKline, S.A. | |||||||||||||
Full Title: REPEAT. Repeated ExPosure To Eltrombopag in Adults with Idiopathic Thrombocytopenic Purpura. An Open-label repeat dosing study of eltrombopag olamine (SB-497115-GR) in adult subjects, with chron... | |||||||||||||
Medical condition: Idiopathic thrombocytopenic purpura (ITP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016203-32 | Sponsor Protocol Number: 20090340 | Start Date*: 2009-11-19 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: An Open Label Study Evaluating the Safety and Efficacy of Long-Term Dosing of Romiplostim in Thrombocytopenic Pediatric Subjects with immune (Idiopathic) Thrombocytopenia Purpura (ITP).------------... | |||||||||||||
Medical condition: Thrombocytopenia in pediatric subjects with ITP---------Sujetos Pediátricos Trombocitopénicos con Púrpura Trombocitopénica Inmune (Idiopática) (PTI) | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014842-28 | Sponsor Protocol Number: SM101-201-itp-09 | Start Date*: 2010-01-06 | |||||||||||
Sponsor Name:SuppreMol GmbH | |||||||||||||
Full Title: A Randomised, Multi-centre, Double-Blind, Placebo-Controlled, Single/Multiple Dose Escalation Phase Ib/IIa Clinical Trial to Investigate the Safety and Efficacy of Recombinant Human Soluble Fc-gamm... | |||||||||||||
Medical condition: Idiopathic Thrombocytopenic Purpura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000961-36 | Sponsor Protocol Number: KB057 | Start Date*: 2013-11-15 | |||||||||||||||||||||
Sponsor Name:Kedrion SpA | |||||||||||||||||||||||
Full Title: Tolerability and safety evaluation of the administration of Ig VENA at high infusion rates. Open label phase III study. | |||||||||||||||||||||||
Medical condition: Patients affected by primary or secondary immunodeficiency (ID) or patients affected by Primary Immune Thrombocytopenia (ITP) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
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