- Trials with a EudraCT protocol (2,928)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,928 result(s) found for: Platelet count.
Displaying page 1 of 147.
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: 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: 2013-005454-30 | Sponsor Protocol Number: C-935788-049 | Start Date*: 2014-11-28 | |||||||||||
Sponsor Name:Rigel Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3 Open Label Extension Study of Fostamatinib Disodium in the Treatment of Persistent/Chronic Immune Thrombocytopenic Purpura | |||||||||||||
Medical condition: Persistent/Chronic Immune Thrombocytopenic Purpura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IT (Completed) HU (Completed) CZ (Completed) AT (Completed) NL (Completed) DK (Completed) ES (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004032-21 | Sponsor Protocol Number: ARGX-113-2004 | Start Date*: 2021-05-07 | |||||||||||
Sponsor Name:argenx BV | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blinded, Placebo-Controlled Trial to Evaluate the Efficacy and the Safety of Efgartigimod (ARGX-113) PH20 Subcutaneous in Adult Patients With Primary Immu... | |||||||||||||
Medical condition: Primary immune thrombocytopenia (ITP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) PT (Completed) DE (Completed) BG (Completed) NO (Completed) DK (Completed) GR (Completed) IT (Completed) FR (Completed) RO (Completed) ES (Prematurely Ended) | |||||||||||||
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: 2008-006143-40 | Sponsor Protocol Number: IP-001 | Start Date*: 2009-07-30 |
Sponsor Name:Medizinische Universität Wien, Universitätsklinik Innere Medizin I | ||
Full Title: Assessment of platelet function in patients with chronic autoimmune thrombocytopenic purpura (cAITP) treated with the thrombopoietin receptor (MPL) agonist Eltrombopag | ||
Medical condition: patients suffering from chronic autoimmune thrombocytopenia the platelet function/activation will be investigated the rise of reticulated platelets and variation of platelet antibodies will be inve... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
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: 2016-003038-26 | Sponsor Protocol Number: ARGX-113-1603 | Start Date*: 2017-02-08 | |||||||||||
Sponsor Name:Argenx BVBA | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Phase II Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of ARGX-113 in Patients with Primary Immune Thrombocytopenia, followed by an Op... | |||||||||||||
Medical condition: Primary Immune Thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) CZ (Completed) BE (Completed) DE (Completed) AT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004012-19 | Sponsor Protocol Number: PRN1008-010(DFI17124) | Start Date*: 2018-03-12 |
Sponsor Name:Principia Biopharma, a Sanofi Company | ||
Full Title: An Adaptive, Open-Label, Dose-Finding, Phase 1/2 Study Investigating the Safety, Pharmacokinetics, and Clinical Activity of Rilzabrutinib (PRN1008), an Oral BTK Inhibitor, in Patients with Relapsed... | ||
Medical condition: Immune Thrombocytopenia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Trial now transitioned) BG (Trial now transitioned) GB (GB - no longer in EU/EEA) NL (Trial now transitioned) NO (Completed) | ||
Trial results: (No results available) |
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: 2019-004103-12 | Sponsor Protocol Number: TAK-079-1004 | Start Date*: 2021-02-22 | |||||||||||
Sponsor Name:Takeda Development Center Americas, Inc. (Takeda) | |||||||||||||
Full Title: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety, Tolerability and Efficacy of TAK-079 in Patients with Persistent/Chronic Primary Immune Thrombocytopenia | |||||||||||||
Medical condition: Primary immune thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SI (Completed) BG (Completed) HR (Completed) IT (Completed) ES (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002471-34 | Sponsor Protocol Number: AZA-MDS-003 | Start Date*: 2012-11-23 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind Study to Compare the Efficacy and Safety of Oral Azacitidine Plus Best Supportive Care Versus Placebo Plus Best Supportive Care in Subjects With Red... | |||||||||||||
Medical condition: Subjects with Red Blood Cell Transfusion-Dependent Anemia and Thrombocytopenia due to IPSS Lower-Risk Myelodysplastic Syndromes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NO (Completed) SE (Completed) ES (Ongoing) CZ (Completed) PT (Completed) LT (Completed) IT (Completed) NL (Completed) GB (GB - no longer in EU/EEA) DE (Completed) FI (Completed) DK (Completed) FR (Completed) GR (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: 2019-004063-49 | Sponsor Protocol Number: NGAM-10 | Start Date*: 2019-10-10 |
Sponsor Name:Octapharma | ||
Full Title: Post-Marketing Study to Evaluate the Efficacy and Safety of PANZYGA in Pediatric Patients with Chronic Immune Thrombocytopenia (ITP) | ||
Medical condition: Chronic Immune Thrombocytopenia | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2018-000017-20 | Sponsor Protocol Number: ASS-Metamizol-DDI | Start Date*: 2018-07-17 |
Sponsor Name:Universitäts-Herzzentrum Freiburg • Bad Krozingen | ||
Full Title: Antiplatelet effect of acetylsalicylic acid in patients after cardiac surgery: Impact of dipyrone (metamizole) | ||
Medical condition: Antithrombotic therapy after surgical replacement of stenotic heart valve by a bioprosthesis or mitral valve repair | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004886-42 | Sponsor Protocol Number: TRA114389 | Start Date*: 2013-04-01 |
Sponsor Name:University of Crete | ||
Full Title: Study of the effect of the thrombopoietin receptor agonist eltrombopag on thrombocytopenia and megakaryopoiesis of patients with lower and intermediate-1 risk myelodysplastic syndromes. | ||
Medical condition: Patients with lower and intermediate-1 risk myelodysplastic syndromes. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-008532-82 | Sponsor Protocol Number: ARC1779-010b | Start Date*: 2009-02-19 |
Sponsor Name:Medical University of Vienna, Dept. of Clinical Pharmacology | ||
Full Title: A Study of the Pharmacodynamics, Pharmacokinetics, and Safety & Efficacy of ARC1779 Injection in Patients with von Willebrand Disease Type 2B | ||
Medical condition: von Willebrand Disease type 2B | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
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 |
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