- Trials with a EudraCT protocol (873)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (46)
873 result(s) found for: Anemia.
Displaying page 13 of 44.
EudraCT Number: 2007-001904-18 | Sponsor Protocol Number: ML21059 | Start Date*: 2007-08-27 | |||||||||||
Sponsor Name:ROCHE FARMA S.A. | |||||||||||||
Full Title: An open label randomised controlled study to compare the efficacy, safety and tolerability of once every four weeks administration of subcutaneous C.E.R.A. versus darboepoetin alfa for the maintena... | |||||||||||||
Medical condition: Anemia en insuficiencia renal crónica | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003777-34 | Sponsor Protocol Number: NL63198.041.17 | Start Date*: 2018-02-09 | |||||||||||||||||||||||||||||||
Sponsor Name:UMC Utrecht | |||||||||||||||||||||||||||||||||
Full Title: Proton pump inhibition for secondary hemochromatosis in hereditary anemia, a phase III placebo controlled randomized cross-over clinical trial. | |||||||||||||||||||||||||||||||||
Medical condition: Iron overload (secondary hemochromatosis) in non-transfusion dependent forms of hereditary anemias. Iron overload and hereditary anemia are a growing, underestimated emerging health care problem. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001876-75 | Sponsor Protocol Number: HOVON103AMLSelinexor | Start Date*: 2016-10-28 | |||||||||||||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||||||||||||
Full Title: A randomized phase II multicenter study with a safety run-in to assess the tolerability and efficacy of the addition of oral selinexor (KPT-330) to standard induction chemotherapy in AML and high r... | |||||||||||||||||||||||
Medical condition: patients ≥ 66 years with: - a diagnosis of AML and related precursor neoplasms according to WHO 2008 classification (excluding acute promyelocytic leukemia) including secondary AML (after an antec... | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) BE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001546-25 | Sponsor Protocol Number: NL48960.029.14 | Start Date*: 2015-01-06 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:VU University Medical Center | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Short versus extended antibiotic treatment with a carbapenem for high-risk febrile neutropenia in hematology patients with Fever of Unknown Origin: a randomized multicenter open-label non-inferiori... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Febrile neutropenia | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005965-20 | Sponsor Protocol Number: ML20938 | Start Date*: 2007-03-07 |
Sponsor Name:Roche AB | ||
Full Title: EFFECTS OF THREE TREATMENT STRATEGIES ON ANEMIA AND QUALITY OF LIFE IN PATIENTS WITH SOLID TUMORS OR LYMPHOPROLIFERATIVE MALIGNANCIES: A RANDOMIZED 3-ARM STUDY ON ACTIVE (A) OR CONVENTIONAL (C) TRA... | ||
Medical condition: Anemia in patients with cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004364-35 | Sponsor Protocol Number: CETB115AUS01T | Start Date*: 2018-07-25 |
Sponsor Name:National Heart, Lung, and Blood | ||
Full Title: Eltrombopag added to standard immunosuppression in treatment-naïve severe aplastic anemia. | ||
Medical condition: Severe aplastic anemia (SAA) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2019-004055-37 | Sponsor Protocol Number: ALXN1830-WAI-201 | Start Date*: 2020-05-06 | |||||||||||
Sponsor Name:Alexion Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Study of ALXN1830 in Patients with Warm Autoimmune Hemolytic Anemia | |||||||||||||
Medical condition: WAIHA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002972-15 | Sponsor Protocol Number: Omalin-01 | Start Date*: 2017-10-06 | |||||||||||
Sponsor Name:Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A. | |||||||||||||
Full Title: Ferrous Acetyl-Aspartylated Casein Formulation Evaluation over Ferrous Sulfate in Iron Deficiency Anemia (Access): A Double-Dummy Randomized Clinical Trial | |||||||||||||
Medical condition: Iron deficiency anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002700-18 | Sponsor Protocol Number: NE-180-201 | Start Date*: 2007-09-25 | |||||||||||
Sponsor Name:Neose Technologies, Inc. | |||||||||||||
Full Title: An Open-Label, Sequential, Ascending dose study, to Evaluate the safety, Pharmacokinetics, and Dose Response, of fixed, Repeated Doses of NE-180 (GlycoPEGylated™rHuEPO) in Anemic Cancer Patients Re... | |||||||||||||
Medical condition: Anaemic cancer patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002270-39 | Sponsor Protocol Number: 205270 | Start Date*: 2018-02-06 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A 28-week, randomized, double-blind, placebo-controlled, parallel-group, multi-center, study in recombinant human erythropoietin (rhEPO) naïve non-dialysis participants with anemia associated with ... | ||
Medical condition: Anaemia associated with chronic kidney disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) PL (Completed) IT (Completed) RO (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-001325-96 | Sponsor Protocol Number: PSO-HEP-2007-01 | Start Date*: 2007-09-04 |
Sponsor Name:Pilar Samper Ots | ||
Full Title: Estudio de dos pautas de hierro intravenoso para la optimización del tratamiento con epoetina recombinante humana en pacientes con anemia inducida por la radio quimioterapia | ||
Medical condition: Anemia en pacientes adultos con tumores sólidos tratados con radio-quimioterapia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003915-73 | Sponsor Protocol Number: 2015/09/21 | Start Date*: 2016-08-19 |
Sponsor Name:Medizinische Universität Wien/Univ.klinik für Innere Medizin III/Abteilung für Nephrologie und Dialyse/Prof Josef Smolen | ||
Full Title: Effect of single dose i.v. iron supplementation on whole-genome transcription in patients with chronic kidney graft failure | ||
Medical condition: Anemia and iron deficiency in renal transplant recipients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002195-14 | Sponsor Protocol Number: KPPM-Hx | Start Date*: 2019-11-12 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:University Hospital "Príncipe de Asturias" | ||||||||||||||||||||||||||||||||||||||
Full Title: Randomized clinical trial to assess the monocitary functionality and their relationship with the administration of intravenous iron in patient in hemodialysis according to practice guidelines or ac... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Monocyte function in patients with anemia in hemodialysis | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004189-17 | Sponsor Protocol Number: ML17249 | Start Date*: 2005-12-22 | |||||||||||
Sponsor Name:N.V. Roche S.A. | |||||||||||||
Full Title: An open-label, single arm, multicenter study to assess the safety and efficacy of once-weekly administration of NeoRecormon using the 30.000 IU prefilled syringe in anaemic adult patients with soli... | |||||||||||||
Medical condition: Anaemia in adult patients with solid tumors treated with non-platinum containing chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005799-15 | Sponsor Protocol Number: ML21438 | Start Date*: 2008-04-08 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: A single arm, open label study to assess the efficacy, safety and tolerability of once-monthly administration of intravenous C.E.R.A. for the maintenance of haemoglobin levels in haemodialysis pati... | |||||||||||||
Medical condition: Chronic renal anemia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005792-34 | Sponsor Protocol Number: 20070782 | Start Date*: 2009-07-09 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Long-term Safety and Efficacy of Darbepoetin Alfa Administered at 500 μg Once-Every-3-Weeks (Q3W) in Anemic Subjects With Advanc... | |||||||||||||
Medical condition: Anemia in subjects with advanced stage non-small cell lung cancer receiving multi-cycle chemotherapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) IE (Prematurely Ended) CZ (Prematurely Ended) AT (Prematurely Ended) BE (Completed) ES (Prematurely Ended) DE (Completed) NL (Prematurely Ended) GR (Prematurely Ended) IT (Prematurely Ended) SI (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004510-33 | Sponsor Protocol Number: BH17847 | Start Date*: 2006-11-15 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A randomized, controlled, open-label, multi-center, parallel-group study to compare the efficacy and safety of RO0503821 with that of darbepoetin alfa administered intravenously at extended dosing ... | |||||||||||||
Medical condition: Chronic renal anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) AT (Completed) FI (Completed) BE (Completed) PT (Completed) NL (Completed) DK (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001193-14 | Sponsor Protocol Number: BAY85-3934/15141 | Start Date*: 2013-12-11 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A randomized, placebo-controlled, double-blind, parallel group, multicenter study to investigate the efficacy and safety of 5 fixed doses of BAY 85- 3934 administered orally in the correction of an... | |||||||||||||
Medical condition: Anaemia of Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) HU (Completed) BG (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004914-18 | Sponsor Protocol Number: CD-001 | Start Date*: 2005-01-21 |
Sponsor Name:ISTITUTO GIANNINA GASLINI | ||
Full Title: A pilot multicentric study for the use of the anti-TNF alfa in patients with: 1) Fanconi Anemia with marrow failure with no bone marrow compatible donor 2) In patients with acquired aplastic anem... | ||
Medical condition: Marrow failure in patients refractary/non eligible to conventional treatments | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000812-41 | Sponsor Protocol Number: GFM-EPO-PRETAR | Start Date*: 2017-12-29 | |||||||||||
Sponsor Name:GFM-Groupe Francophone des Myélodysplasies | |||||||||||||
Full Title: A RANDOMIZED TRIAL TESTING EARLY VERSUS LATE ONSET OF EPO ALFA TREATMENT IN LOWER RISK MDS WITH NON RBC TRANSFUSION DEPENDENT ANEMIA AND WITHOUT DEL 5Q | |||||||||||||
Medical condition: Adult subject (18 years of age older) with low or intermediate-1 IPSS risk MDS with transfusions independent anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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