- Trials with a EudraCT protocol (526)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
526 result(s) found for: Platelet disorders.
Displaying page 1 of 27.
| EudraCT Number: 2013-000965-34 | Sponsor Protocol Number: E5501-G000-310 | Start Date*: 2014-05-27 | ||||||||||||||||||||||||||
| Sponsor Name:Eisai Limited | ||||||||||||||||||||||||||||
| Full Title: A Randomized, Global, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy and Safety of Once-daily Oral Avatrombopag for the Treatment of Adults with Thrombocytopenia ... | ||||||||||||||||||||||||||||
| Medical condition: Thrombocytopenia in Patients with Chronic Liver Disease | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) IT (Completed) GB (Completed) AT (Completed) HU (Completed) ES (Completed) PT (Completed) PL (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2013-000934-36 | Sponsor Protocol Number: E5501-G000-311 | Start Date*: 2014-06-16 | ||||||||||||||||||||||||||
| Sponsor Name:Eisai Limited | ||||||||||||||||||||||||||||
| Full Title: A Randomized, Global, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy and Safety of Once-daily Oral Avatrombopag for the Treatment of Adults with Thrombocytopenia ... | ||||||||||||||||||||||||||||
| Medical condition: Thrombocytopenia in Patients with Chronic Liver Disease | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) IT (Completed) ES (Completed) CZ (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 | ||||||||||||||||||||||||||||
| EudraCT Number: 2020-003232-24 | Sponsor Protocol Number: AVA-PED-301 | Start Date*: 2020-12-03 | ||||||||||||||||||||||||||
| Sponsor Name:Dova Pharmaceuticals, Inc. | ||||||||||||||||||||||||||||
| Full Title: A Phase 3b, Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel-group Trial with an Open-label Extension Phase to Evaluate the Efficacy and Safety of Avatrombopag for the Treatment... | ||||||||||||||||||||||||||||
| Medical condition: Thrombocytopenia in paediatric subjects with immune thrombocytopenia for ≥6 months duration who have had an insufficient response to a previous treatment | ||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Completed) HU (Completed) DE (Completed) PL (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2010-024479-20 | Sponsor Protocol Number: E5501-G000-203 | Start Date*: 2011-11-24 | ||||||||||||||||||||||||||
| Sponsor Name:Eisai Limited | ||||||||||||||||||||||||||||
| Full Title: A Phase 2, Randomized, Multicenter, Placebo-Controlled, Double-Blind, Parallel-Group Study, with an Open-Label Extension to Evaluate the Efficacy, Safety, and Pharmacokinetics of E5501 in Subjects ... | ||||||||||||||||||||||||||||
| Medical condition: Thrombocytopenia associated with chronic hepatitis C virus | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) BG (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2020-000968-30 | Sponsor Protocol Number: RC31/19/0509 | Start Date*: 2021-04-13 | |||||||||||
| Sponsor Name:CHU Toulouse | |||||||||||||
| Full Title: ASPirin in Immune thRombocytopenia patients with cardiovascular disEase | |||||||||||||
| Medical condition: Immune thrombocytopenia with cardiovascular disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-002896-32 | Sponsor Protocol Number: D5136C00001 | Start Date*: 2013-01-16 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A multicenter, double-blind, placebo-controlled, pharmacokinetic, pharmacodynamic, safety and tolerability study in patients aged 12 to <18 years of age with a central venous catheter to support pr... | |||||||||||||
| Medical condition: Thrombosis, thromboembolism | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-020219-35 | Sponsor Protocol Number: | Start Date*: 2011-07-18 |
| Sponsor Name:Royal Brompton & Harefield NHS Foundation Trust | ||
| Full Title: Evaluating the benefit of additional platelet inhibition in acute coronary syndrome patients with high platelet reactivity undergoing PCI | ||
| Medical condition: Cardiovascular disease - Acute coronary syndrome | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003653-17 | Sponsor Protocol Number: 992 | Start Date*: 2017-01-27 | |||||||||||
| Sponsor Name:Biotest AG | |||||||||||||
| Full Title: An open label, prospective, randomized, multicenter study investigating clinical efficacy and safety of the human normal immunoglobulin for intravenous administration BT595 in patients with chronic... | |||||||||||||
| Medical condition: Chronic primary immune thrombocytopenia (ITP) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) ES (Completed) CZ (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004162-18 | Sponsor Protocol Number: PDY16894 | Start Date*: 2021-03-16 | |||||||||||
| Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
| Full Title: A multicenter, Phase 2a, open-label, non-randomized study evaluating the efficacy, safety, and tolerability of BIVV020 in adults with persistent/chronic immune thrombocytopenia (ITP) | |||||||||||||
| Medical condition: immune thrombocytopenia (ITP) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) CZ (Completed) NL (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014858-15 | Sponsor Protocol Number: TRC112765 | Start Date*: 2010-10-27 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
| Full Title: A Randomized, Blinded, Placebo-controlled, Two-Phase, Sequential Cohort, Dose Finding Study to Assess the Safety and Efficacy of an Oral Thrombopoietin Receptor Agonist, Eltrombopag (SB-497115-GR),... | |||||||||||||
| Medical condition: chemotherapy induced thrombocytopenia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) IE (Completed) GR (Completed) FI (Completed) HU (Completed) CZ (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 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: 2012-000397-30 | Sponsor Protocol Number: PLASMAFIST-2011 | Start Date*: 2013-02-07 | |||||||||||
| Sponsor Name:FUNDACIÓN CANARIA DE INVESTIGACIÓN Y SALUD (FUNCIS) | |||||||||||||
| Full Title: CLINICAL ASSESSMENT OF THE EFFECTS OF AUTOLOGOUS PLATELET-POOR PLASMA ON PREVENTION OF BRONCHOPLEURAL FISTULA AND LUNG DAMAGE IN PATIENTS UNDERGOING LUNG RESECTION SURGERY | |||||||||||||
| Medical condition: Bronchopleural fistula | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004942-91 | Sponsor Protocol Number: 1423M0634 | Start Date*: 2015-06-17 | |||||||||||
| Sponsor Name:Shionogi Ltd | |||||||||||||
| Full Title: A Phase 3 Randomised, Double-blind, Placebo-controlled Study to Assess the Safety and Efficacy of S-888711 (Lusutrombopag) for the Treatment of Thrombocytopenia in Patients with Chronic Liver Disea... | |||||||||||||
| Medical condition: Thrombocytopenia in patients with Chronic Liver Disease (CLD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) AT (Completed) HU (Completed) DE (Completed) BE (Completed) IT (Completed) ES (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004657-11 | Sponsor Protocol Number: VI-Plt-01 | Start Date*: 2012-03-30 | |||||||||||
| Sponsor Name:FONDAZIONE PROGETTO EMATOLOGIA | |||||||||||||
| Full Title: Open label multicenter study of Eltrombopag for the treatment of Immune ThrombocytoPenia (ITP) secondary to Chronic Lymphoproliferative Disorders (LPDs) | |||||||||||||
| Medical condition: Immune ThrombocytoPenia (ITP) secondary to Chronic Lymphoproliferative Disorders (LPDs) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001636-22 | Sponsor Protocol Number: TROPICALACS | Start Date*: 2013-08-26 | |||||||||||
| Sponsor Name:Hospital of the University of Munich, Grosshadern | |||||||||||||
| Full Title: A prospective, randomized, parallel-group, open label, non-inferiority, multicenter trial of a 12 month vs. a short-term platelet function testing guided prasugrel therapy in acute coronary syndrom... | |||||||||||||
| Medical condition: Troponin positive acute coronary syndrome after successful percutaneous coronary intervention with an indication for a standard treatment of 12 month with prasugrel | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) AT (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004683-22 | Sponsor Protocol Number: RGCH005 | Start Date*: 2020-10-16 | |||||||||||
| Sponsor Name:Ostfold Hospital Trust | |||||||||||||
| Full Title: Daratumumab as a treatment for adult immune thrombocytopenia | |||||||||||||
| Medical condition: Immune thrombocytopenia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) FR (Completed) DK (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 (Trial now transitioned) GB (GB - no longer in EU/EEA) PL (Trial now transitioned) AT (Completed) NO (Trial now transitioned) FR (Trial now transitioned) HU (Trial now transitioned) IT (Trial now transitioned) NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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