- Trials with a EudraCT protocol (1,407)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,407 result(s) found for: Blood group system.
Displaying page 1 of 71.
EudraCT Number: 2017-002919-33 | Sponsor Protocol Number: 207911 | Start Date*: 2018-03-09 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: Phase IV, open-label, randomized study to enrol healthy adult volunteers, naïve to any previous meningococcal vaccination or meningococcal disease, aged 18-50 years, to be either vaccinated with GS... | |||||||||||||
Medical condition: Meningitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005685-30 | Sponsor Protocol Number: LA38-EXT | Start Date*: 2015-09-18 | |||||||||||
Sponsor Name:ApoPharma Inc. | |||||||||||||
Full Title: Long-term safety and efficacy study of Ferriprox® for the treatment of transfusional iron overload in patients with sickle cell disease or other anemias. | |||||||||||||
Medical condition: Iron overload in sickle cell disease or other anemias | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000501-22 | Sponsor Protocol Number: SPON1189-13 | Start Date*: 2013-10-30 | |||||||||||
Sponsor Name:Cardiff Univeristy | |||||||||||||
Full Title: A national cancer research institute acute myeloid leukaemia working group pilot trial under the auspices of the cardiff experimental cancer medicine centre to establish the feasibility of combinin... | |||||||||||||
Medical condition: Acute Myeloid Leukaemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2010-019237-10 | Sponsor Protocol Number: FARM8MR2J7 | Start Date*: 2010-10-28 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Multicenter prospective randomized open with a blinded end point (PROBE) parallel-group study on treatment with biphasic insulin BIAsp70/30 and short-acting insulin or rapid-acting analogue plus gl... | |||||||||||||
Medical condition: DM1 | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003585-14 | Sponsor Protocol Number: SNOXH94C301 | Start Date*: 2014-01-10 | |||||||||||||||||||||
Sponsor Name:NOXXON Pharma AG | |||||||||||||||||||||||
Full Title: Safety, PK/PD and efficacy of NOX-H94 in dialysis patients with ESA-hyporesponsive anaemia: A randomized, double blind, placebo controlled parallel group study with a single blind cross-over group | |||||||||||||||||||||||
Medical condition: Erythropoiesis stimulating agents (ESA) hyporesponsive anaemia in renal dialysis patients | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) AT (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-003027-15 | Sponsor Protocol Number: EFFI2021/01 | Start Date*: 2023-03-20 | |||||||||||
Sponsor Name:ITALFARMACO S.P.A. | |||||||||||||
Full Title: A multicentre, prospective, open-label, non-comparative study to evaluate menstrual bleeding typology, tolerability, and compliance during a monophasic hormonal contraceptive treatment with norgest... | |||||||||||||
Medical condition: Combined Oral Contraceptives (COC) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003372-31 | Sponsor Protocol Number: LJ401-BT01 | Start Date*: 2018-03-20 | |||||||||||
Sponsor Name:La Jolla Pharmaceutical Company | |||||||||||||
Full Title: A Multi-center, Randomized, Open-Label, Parallel-Group Study with LJPC-401 for the Treatment of Myocardial Iron Overload in Patients with Transfusion-Dependent Beta Thalassemia | |||||||||||||
Medical condition: Transfusion-dependent beta thalassemia with myocardial iron overload | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) GR (Completed) CY (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001221-14 | Sponsor Protocol Number: E.G.R.A.B.I.N.S1 | Start Date*: 2016-06-17 | |||||||||||
Sponsor Name:Herlev Gentofte Hospital | |||||||||||||
Full Title: Effect of glucagon-like peptide 1 (GLP-1) based diabetes medication on blood flow velocity in persons without cerebrovascular disease. | |||||||||||||
Medical condition: This is a healthy control group which is to be compared with patients with stroke. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001544-26 | Sponsor Protocol Number: RASCOVID-19 | Start Date*: 2020-04-22 | ||||||||||||||||
Sponsor Name:Center for Clinical Metabolic Research, Gentofte Hospital | ||||||||||||||||||
Full Title: Effects of discontinuing renin-angiotensin system inhibitors in patients with and without COVID-19 | ||||||||||||||||||
Medical condition: Coronavirus disease 2019 (COVID-19) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000236-26 | Sponsor Protocol Number: CRLX030X2201 | Start Date*: 2012-11-06 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An exploratory study to investigate the haemodynamic effects of serelaxin in patients with compensated cirrhosis and portal hypertension | |||||||||||||
Medical condition: Compensated alcohol-related cirrhosis and portal hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000276-23 | Sponsor Protocol Number: 201464 | Start Date*: 2016-12-06 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||||||||||||||||||
Full Title: A multiple treatment session, open label phase 2 clinical study of GSK2398852 administered following and together with GSK2315698 in cohorts of patients with cardiac amyloidosis | ||||||||||||||||||
Medical condition: Systemic amyloidosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (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: 2012-004622-14 | Sponsor Protocol Number: LPS_concmed_controlled | Start Date*: 2013-02-01 |
Sponsor Name:Radboud University Nijmegen Medical Centre | ||
Full Title: Concentration/meditation as a novel means to limit inflammation: a randomized controlled pilot study | ||
Medical condition: Possibe future indications: inflammatory conditions in general, auto-immune diseases | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005679-18 | Sponsor Protocol Number: GMX04 | Start Date*: 2011-12-07 | |||||||||||
Sponsor Name:Bio Products Laboratory Limited | |||||||||||||
Full Title: A Phase IV, Multicenter, Open-Label Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Gammaplex in Primary Immunodeficiency Diseases (PID) in Children and Adolescents | |||||||||||||
Medical condition: Primary immunodeficiency diseases | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2014-004032-19 | Sponsor Protocol Number: NLOCEAN.505.14 | Start Date*: 2015-09-09 |
Sponsor Name:Radboud University Medical Center | ||
Full Title: A randomised, open-label clinical trial assessing the efficacy of octreotide to decrease iron infusion and blood transfusion requirements in patients with refractory anaemia due to gastrointestinal... | ||
Medical condition: small bowel angiodysplasias | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002908-39 | Sponsor Protocol Number: FEPODPara2020-1 | Start Date*: 2020-10-30 |
Sponsor Name:Helsinki University Hospital | ||
Full Title: Detection of paracetamol concentration in blood-, saline- and urine samples with an electrochemical indicator in healthy volunteers - a validation study for a novel technique. | ||
Medical condition: This is a laboratory equipment validation study. All subjects are healthy volunteered individuals. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003486-15 | Sponsor Protocol Number: SP0934 | Start Date*: 2012-06-13 | |||||||||||
Sponsor Name:UCB BIOSCIENCES GmbH | |||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo-controlled, parallel group, polysomnography study to investigate safety and efficacy of the rotigotine transdermal patch in subjects with Restless ... | |||||||||||||
Medical condition: Restless Legs Syndrome in patients with End Stage Renal Disease (ESRD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004433-24 | Sponsor Protocol Number: 59498 | Start Date*: 2017-05-17 |
Sponsor Name:Leids Universitair Medisch Centrum | ||
Full Title: ACE inhibition in Fontan patients: its effect on body fluid regulation. | ||
Medical condition: Patients with univentricular hearts palliated by the Fontan procedure | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001268-40 | Sponsor Protocol Number: HAVEN | Start Date*: 2020-01-23 | |||||||||||
Sponsor Name:Guy's and St. Thomas' NHS Foundation Trust | |||||||||||||
Full Title: Hydroxychloroquine in ANCA Vasculitis Evaluation - A Multicentre, Randomised, Double-blind, Placebo-controlled Trial | |||||||||||||
Medical condition: The term ANCA-associated vasculitis (AAV) describes a subset of primary small vessel vasculitides characterized by the presence of anti-neutrophil cytoplasmic antibodies (ANCA): Granulomatosis with... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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