- 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 2 of 3.
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 |
EudraCT Number: 2015-005276-14 | Sponsor Protocol Number: RGCH004 | Start Date*: 2016-12-08 | |||||||||||
Sponsor Name:Sykehuset Østfold HF | |||||||||||||
Full Title: Prolonging the response by low-dose Rituximab maintenance therapy in immune thrombocytopenia: a randomized placebo-controlled trial- the PROLONG trial. | |||||||||||||
Medical condition: Immune thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002946-13 | Sponsor Protocol Number: TRA108062 | Start Date*: 2009-07-30 | |||||||||||
Sponsor Name:GlaxoSmithKline S.A. | |||||||||||||
Full Title: A three part, staggered cohort, open-label and double blind, randomized, placebo controlled study to investigate the efficacy, safety, tolerability and pharmacokinetics of eltrombopag, a thrombopoi... | |||||||||||||
Medical condition: Chronic Idiopathic Thrombocytopenic Purpura Púrpura Trombocitopénica Idiopática Crónica | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) FR (Completed) NL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004347-10 | Sponsor Protocol Number: 20080009 | Start Date*: 2009-06-17 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Prospective, Phase IV, Open-Label, Multi-Center Study Evaluating Changes in Bone Marrow Morphology in Adult Subjects Receiving Romiplostim for the Treatment of Thrombocytopenia Associated with Im... | |||||||||||||
Medical condition: Thrombocytopenia associated with ITP | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) CZ (Completed) DE (Completed) PL (Completed) BE (Completed) ES (Completed) HU (Completed) SE (Completed) EE (Completed) IT (Completed) LT (Completed) SI (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002184-17 | Sponsor Protocol Number: TRA115450 | Start Date*: 2012-02-08 | |||||||||||
Sponsor Name:Glaxosmithkline Research and Development Ltd | |||||||||||||
Full Title: A two part, double-blind, randomized, placebo-controlled and open-label study to investigate the efficacy, safety and tolerability of eltrombopag, a thrombopoietin receptor agonist, in pediatric pa... | |||||||||||||
Medical condition: To assess the efficacy of eltrombopag, relative to placebo, in achieving platelet counts of ≥ 50 Gi/L, when administered to pediatric subjects with previously treated chronic ITP during the first 1... | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) ES (Completed) GB (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001371-20 | Sponsor Protocol Number: 200170 | Start Date*: 2013-09-06 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | ||||||||||||||||||
Full Title: Study 200170: A Rollover Study to Provide Continued Treatment with Eltrombopag | ||||||||||||||||||
Medical condition: Acute myelogenous leukemia & Idiopathic thrombocytopenic purpura (ITP | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Completed) ES (Completed) BE (Completed) GR (Completed) PL (Completed) NL (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005918-20 | Sponsor Protocol Number: ITP001 | Start Date*: 2008-12-23 | |||||||||||
Sponsor Name:Rikshospitalet | |||||||||||||
Full Title: Rituximab as second line treatment for ITP: A Multicentre, Randomized, Double blind, Placebo-controlled, Phase III study. “The RITP study” | |||||||||||||
Medical condition: Immune thrombocytopenic purpura (ITP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019375-30 | Sponsor Protocol Number: ALX-0681-2.1/10 | Start Date*: 2010-09-07 | |||||||||||
Sponsor Name:Ablynx | |||||||||||||
Full Title: A Phase II single blind, randomized, placebo controlled trial to study the efficacy and safety of anti-von Willebrand factor Nanobody administered as adjunctive treatment to patients with acquired ... | |||||||||||||
Medical condition: Acquired thrombotic thrombocytopenic purpura (TTP) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) AT (Completed) GB (Completed) DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000470-78 | Sponsor Protocol Number: TRA102537 | Start Date*: 2006-10-30 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Limited | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled phase III study, to evaluate the efficacy, safety and tolerability of eltrombopag olamine (SB-497115-GR), a thrombopoietin receptor agonist, administe... | |||||||||||||
Medical condition: Idiopathic thrombocytopenic purpura (ITP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FI (Completed) DK (Completed) FR (Completed) AT (Completed) CZ (Completed) SK (Completed) DE (Completed) GR (Completed) IT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002478-11 | Sponsor Protocol Number: 2.0 | Start Date*: 2016-07-19 | |||||||||||||||||||||
Sponsor Name:Medical University of Vienna, Department of Internal medicine I | |||||||||||||||||||||||
Full Title: Very low doses of Rituximab for off-label treatment – a Pilot Trial | |||||||||||||||||||||||
Medical condition: Autoimmune-haemolytic Anemia Antiphospholipid Syndrome Immune-mediated Thrombocytopenia | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004371-19 | Sponsor Protocol Number: ARC1779-004 | Start Date*: 2007-11-20 | ||||||||||||||||
Sponsor Name:Archemix Corp. | ||||||||||||||||||
Full Title: A Phase 2 Pilot Study of the Safety, Pharmacokinetics, and Pharmacodynamics of ARC1779 Injection in Patients with von Willebrand Factor-Related Platelet Function Disorders | ||||||||||||||||||
Medical condition: von Willebrand Factor- related platelet function disorders : thrombotic thrombocytopenic purpura(TTP) in remission, acute TTP, and von Willebrand Disease Type- 2b (vWD-2b). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005586-21 | Sponsor Protocol Number: GMX02 | Start Date*: 2011-12-07 | |||||||||||
Sponsor Name:Bio Products Laboratory Limited | |||||||||||||
Full Title: A Phase III, Multicenter, Open-Label Study To Evaluate the Efficacy and Safety of GAMMAPLEX® in Chronic Idiopathic Thrombocytopenic Purpura | |||||||||||||
Medical condition: Idiopathic thrombocytopenic purpura. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005871-92 | Sponsor Protocol Number: Sahlgrenska/Hematology/2008:1 | Start Date*: 2009-02-05 | |||||||||||
Sponsor Name:Sahlgrenska University Hospital | |||||||||||||
Full Title: En fas 1 studie av effekt av Tysabri (natalizumab), en IgG4 humaniserad monoklonal antikropp specifik mot VLA-4 (integrin alfa-4), administrerad som infusion 1 gång/månad under 3 månader hos patie... | |||||||||||||
Medical condition: Chronic idiopathic thrombocytopenic purpura (ITP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003534-32 | Sponsor Protocol Number: MOM-M254-001 | Start Date*: 2019-01-03 | |||||||||||
Sponsor Name:Momenta Pharmaceuticals, Inc. | |||||||||||||
Full Title: A 4-part Phase 1/2 study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of M254 in healthy volunteers and in patients with immune thrombocytopenic purpura | |||||||||||||
Medical condition: Immune thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) HU (Completed) PL (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000173-65 | Sponsor Protocol Number: 20030212 | Start Date*: 2005-04-07 |
Sponsor Name:Amgen Inc | ||
Full Title: A Randomized, Placebo Controlled Study Evaluating the Efficacy and Safety of AMG 531 Treatment of Thrombocytopenic Subjects with Immune (Idiopathic) Thrombocytopenic Purpura (ITP) Prior to Splenectomy | ||
Medical condition: Thrombocytopenia in subjects with Immune Thrombocytopenic Purpura (ITP) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000174-31 | Sponsor Protocol Number: 20030105 | Start Date*: 2005-04-07 |
Sponsor Name:Amgen Inc | ||
Full Title: A Randomized, Placebo Controlled Study Evaluating the Efficacy and Safety of AMG 531 Treatment of Thrombocytopenic Subjects with Immune (Idiopathic) Thrombocytopenic Purpura (ITP) Refractory to Spl... | ||
Medical condition: Thrombocytopenia in subjects with Immune Thrombocytopenic Purpura (ITP) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002063-60 | Sponsor Protocol Number: PRN1008-018(EFC17093) | Start Date*: 2020-11-12 | |||||||||||
Sponsor Name:Principia Biopharma, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-Controlled, Parallel-Group Study with an Open-Label Extension to Evaluate the Efficacy and Safety of Oral Rilzabrutinib (PRN1008) in Adults... | |||||||||||||
Medical condition: Immune Thrombocytopenia (ITP) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) GB (GB - no longer in EU/EEA) PL (Ongoing) AT (Completed) NO (Ongoing) FR (Trial now transitioned) HU (Ongoing) IT (Ongoing) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000471-14 | Sponsor Protocol Number: TRA105325 | Start Date*: 2006-06-13 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: EXTEND (Eltrombopag eXTENded Dosing Study): An extension study of eltrombopag olamine (SB-497115-GR) in adults, with idiopathic thrombocytopenic purpura (ITP), previously enrolled in an eltrombopa... | ||
Medical condition: Immune thrombocytopenic purpura (ITP) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SI (Completed) SE (Completed) DE (Completed) ES (Completed) IE (Completed) NL (Completed) GR (Completed) FR (Completed) SK (Completed) GB (Completed) CZ (Completed) DK (Completed) IT (Completed) FI (Completed) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-000830-12 | Sponsor Protocol Number: E5501-G000-302 | Start Date*: 2012-08-28 | ||||||||||||||||||||||||||
Sponsor Name:Eisai Limited | ||||||||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Trial with an Open-label Extension Phase to Evaluate the Efficacy and Safety of Oral E5501 Plus Standard of Care... | ||||||||||||||||||||||||||||
Medical condition: Chronic Immune Thrombocytopenia (Idiopathic Thrombocytopenic Purpura) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) SK (Completed) BE (Completed) CZ (Completed) PL (Completed) BG (Completed) GR (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000831-10 | Sponsor Protocol Number: E5501-G000-305 | Start Date*: 2012-07-16 | ||||||||||||||||||||||||||
Sponsor Name:Eisai Limited | ||||||||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Active-controlled, Parallel-group Trial with an Open-label Extension Phase to Evaluate the Efficacy and Safety of Oral E5501 versus Eltrombopag, i... | ||||||||||||||||||||||||||||
Medical condition: Chronic Immune Thrombocytopenia (Idiopathic Thrombocytopenic Purpura) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) NL (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
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