- Trials with a EudraCT protocol (684)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
684 result(s) found for: Terminal disease.
Displaying page 5 of 35.
EudraCT Number: 2012-004888-41 | Sponsor Protocol Number: IPeRStudy | Start Date*: 2012-12-28 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Intensive Phosphate Control in Development of Renal End Points and Mortality in CKD (the IPeR Study) | |||||||||||||
Medical condition: Patients with Chronic Kidney Disease (CKD) not yet on dialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004641-25 | Sponsor Protocol Number: 201700823 | Start Date*: 2019-04-30 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Rotation for Optimal Targeting of Albuminuria and Treatment Evaluation. | ||
Medical condition: Proteinuric Kidney disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004152-10 | Sponsor Protocol Number: EMPATHY | Start Date*: 2020-01-30 | ||||||||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | ||||||||||||||||||
Full Title: Evaluating the Short-Term Renal and Systemic Effects of SGLT2 Inhibition in Non-Diabetic Patients at Risk of Accelerated GFR Decline Because of Glomerular Hyperfiltration: a sequential OFF-ON-OFF S... | ||||||||||||||||||
Medical condition: Obesity Renal chronic disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004183-21 | Sponsor Protocol Number: IP-001-18 | Start Date*: 2022-08-19 | |||||||||||
Sponsor Name:Iperboreal Pharma Srl | |||||||||||||
Full Title: A Study to Evaluate the EffIcacy and Safety of XyloCore, a Glucose Sparing Experimental Solution, for Peritoneal Dialysis | |||||||||||||
Medical condition: End-Stage Renal Disease (ESRD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) DK (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000126-46 | Sponsor Protocol Number: ML20888 | Start Date*: 2007-11-05 | |||||||||||
Sponsor Name:Roche Pharma AG | |||||||||||||
Full Title: Einarmige, offene Studie zur Untersuchung der Wirksamkeit, Sicherheit und Verträglichkeit von monatlich subkutan verabreichtem C.E.R.A. an Patienten mit renaler Anämie, die noch nicht dialysepflich... | |||||||||||||
Medical condition: renal anemia due to chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000457-34 | Sponsor Protocol Number: FG-506-02-40 | Start Date*: 2004-10-19 | |||||||||||
Sponsor Name:Fujisawa GmbH | |||||||||||||
Full Title: A MULTICENTRE, RANDOMISED, OPEN CLINICAL STUDY TO COMPARE THE EFFICACY AND SAFETY OF A COMBINATION THERAPY OF TACROLIMUS WITH SIROLIMUS VERSUS TACROLIMUS WITH MYCOPHENOLATE MOFETIL IN KIDNEY TRANSP... | |||||||||||||
Medical condition: Patients with end stage kidney disease who will undergo primary renal transplantation or retransplantation. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) AT (Completed) ES (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000520-32 | Sponsor Protocol Number: FG-506-02-42 | Start Date*: 2005-01-26 | |||||||||||
Sponsor Name:Fujisawa GmbH | |||||||||||||
Full Title: A MULTICENTRE, RANDOMISED, OPEN CLINICAL STUDY TO COMPARE THE EFFICACY AND SAFETY OF A COMBINATION OF TACROLIMUS AND MYCOPHENOLATE MOFETIL BASED REGIMEN WITH OR WITHOUT INDUCTION IN ELDERLY RECIPIE... | |||||||||||||
Medical condition: Patients with end stage kidney disease who will undergo primary renal transplantion or retransplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000726-10 | Sponsor Protocol Number: ADAPT | Start Date*: 2021-06-23 | |||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | |||||||||||||
Full Title: Evaluating the short-term renal and systemic effects of Dapagliflozin in non-diabetic patients with stage IV CKD at risk of ESKD because of severe renal insufficiency and persistent proteinuria: A ... | |||||||||||||
Medical condition: Non-diabetic stage IV Chronic Kidney Disease (CKD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006994-10 | Sponsor Protocol Number: SEQ-ALO-2007-01 | Start Date*: 2009-02-04 | ||||||||||||||||
Sponsor Name:Fundación Investigación Biomédica Hospital Príncipe de Asturias | ||||||||||||||||||
Full Title: Evaluación de la utilidad del alopurinol en la prevención de la morbimortalidad cardiovascular de los pacientes con enfermedad renal crónica (ERC) e hiperuricemia EVALUATION OF THE USE OF ALLOPURI... | ||||||||||||||||||
Medical condition: Enfermedad renal crónica (ERC) e hiperuricemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005365-35 | Sponsor Protocol Number: 1449 | Start Date*: 2008-07-20 | |||||||||||
Sponsor Name:Fresenius Medical Care Deutschland GmbH | |||||||||||||
Full Title: Multicentric, parallel, controlled, randomized, single blind clinical evaluation of a new low sodium peritoneal dialysis solution on patients with hypertension treated with continous ambulatory or... | |||||||||||||
Medical condition: Subjects with renal failure treated with peritoneal dialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) FR (Completed) DK (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000142-37 | Sponsor Protocol Number: XM01-06 | Start Date*: 2005-06-13 | |||||||||||
Sponsor Name:BioGeneriX AG | |||||||||||||
Full Title: Efficacy and Safety of subcutaneous administration of XM01 compared to Epoetin beta in anaemic chronic renal failure patients not yet receiving dialysis and in maintenance phase treatment with Epoe... | |||||||||||||
Medical condition: anaemic chronic renal failure patients not yet receiving dialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002263-54 | Sponsor Protocol Number: D7551C00001 | Start Date*: 2021-03-19 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase 2b Randomised, Double-Blind, Placebo-Controlled, Multi-Centre, Dose-Ranging Study of AZD5718 in Participants with Proteinuric Chronic Kidney Disease | |||||||||||||
Medical condition: Proteinuric Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) HU (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004989-17 | Sponsor Protocol Number: KRM-306 | Start Date*: 2007-10-17 | |||||||||||
Sponsor Name:Mitsubishi Tanabe Pharma Corporation [...] | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of AST-120 for Prevention of Chronic Kidney Disease Progression in Patients with Moderate to Severe Chronic Kidney Disease | |||||||||||||
Medical condition: Moderate to Severe Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004990-13 | Sponsor Protocol Number: KRM-307 | Start Date*: 2007-10-17 | |||||||||||
Sponsor Name:Mitsubishi Tanabe Pharma Corporation [...] | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of AST-120 for Prevention of Chronic Kidney Disease Progression in Patients with Moderate to Severe Chronic Kidney Disease includin... | |||||||||||||
Medical condition: Moderate to Severe Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000289-16 | Sponsor Protocol Number: REGEN-016 | Start Date*: 2023-04-11 | |||||||||||
Sponsor Name:ProKidney | |||||||||||||
Full Title: A PHASE 3 RANDOMIZED CONTROLLED STUDY OF REACT IN PARTICIPANTS WITH TYPE 2 DIABETES AND CHRONIC KIDNEY DISEASE (REGEN-016) | |||||||||||||
Medical condition: TYPE 2 DIABETES AND CHRONIC KIDNEY DISEASE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) AT (Prematurely Ended) BE (Completed) PT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021358-20 | Sponsor Protocol Number: A7331011 | Start Date*: 2011-03-07 | |||||||||||
Sponsor Name:Pfizer Inc. 235 east 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP, MULTI-CENTER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ONCE-DAILY ADMINISTRATION OF A PHOSPHODIESTERASE 5 INHIBITOR (PF-0... | |||||||||||||
Medical condition: Chronic kidney disease (CKD), also known as chronic renal disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) PL (Completed) SK (Completed) SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002013-34 | Sponsor Protocol Number: 214066 | Start Date*: 2023-03-27 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: An Integrated Pharmacokinetic and Safety Open-label Basket Trial of Daprodustat for the Treatment of Anemia Associated with Chronic Kidney Disease in Male and Female Children and Adolescents Aged 3... | |||||||||||||
Medical condition: Anemia associated with chronic kidney disease (CKD) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Prematurely Ended) FR (Completed) AT (Prematurely Ended) BE (Completed) PL (Prematurely Ended) Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019388-12 | Sponsor Protocol Number: AMAG-FER-CKD-252 | Start Date*: 2011-05-12 | |||||||||||
Sponsor Name:AMAG Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Open-Label, Active-Controlled Study of the Safety, Efficacy, and Pharmacokinetics of Ferumoxytol Compared with Oral Iron for the Treatment of Iron Deficiency Anemia in Pediatric Subje... | |||||||||||||
Medical condition: Nondialysis dependent Chronic Kidney Disease | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) RO (Ongoing) LT (Prematurely Ended) ES (Temporarily Halted) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019550-40 | Sponsor Protocol Number: AMAG-FER-CKD-253 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:AMAG Pharmaceuticals, Inc. | |||||||||||||
Full Title: An Open-Label Extension Study of the Safety and Efficacy of Ferumoxytol for the Episodic Treatment of Iron Deficiency Anemia in Pediatric Subjects with Chronic Kidney Disease | |||||||||||||
Medical condition: Chronic Kidney Disease | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Prematurely Ended) HU (Completed) ES (Completed) RO (Temporarily Halted) LT (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002682-19 | Sponsor Protocol Number: PHI113633 | Start Date*: 2013-12-20 | |||||||||||
Sponsor Name:GlaxoSmithKline, S.A. | |||||||||||||
Full Title: A Phase 2B, randomized, blinded, dose-ranging, active-controlled, parallel-group, multi-center study to evaluate the dose response relationship of GSK1278863 over the first 4 weeks of treatment and... | |||||||||||||
Medical condition: Anemia associated with chronic kidney disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) CZ (Completed) GB (Completed) DK (Completed) HU (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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