- Trials with a EudraCT protocol (747)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
747 result(s) found for: Chronic Kidney Disease.
Displaying page 19 of 38.
EudraCT Number: 2020-005186-13 | Sponsor Protocol Number: CLNP023F12301 | Start Date*: 2021-08-26 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A multicenter, single-arm, open label trial to evaluate efficacy and safety of oral, twice daily LNP023 in adult aHUS patients who are naive to complement inhibitor therapy | |||||||||||||
Medical condition: atypical hemolytic uremic syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) SI (Trial now transitioned) CZ (Trial now transitioned) SK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005728-34 | Sponsor Protocol Number: 2006-66-INJ-14 | Start Date*: 2008-02-27 | |||||||||||
Sponsor Name:Hexal Biotech ForschungsGmbH | |||||||||||||
Full Title: Post authorisation safety study to prospectively monitor the incidence of relevant drug-related adverse events and EPO-related lack of efficacy among CKD subjects receiving HX575 recombinant human ... | |||||||||||||
Medical condition: Chronic kidney disease subjects with or without dialysis treatment and requiring i.v. ESA treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) IT (Completed) FR (Completed) GB (Prematurely Ended) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004851-36 | Sponsor Protocol Number: 404-201-00012 | Start Date*: 2020-08-25 | |||||||||||||||||||||
Sponsor Name:Otsuka Pharmaceutical (OPDC) | |||||||||||||||||||||||
Full Title: Phase 3b, Randomized, Open-label, Active-controlled Trial Evaluating the Efficacy and Safety of Oral Vadadustat Once Daily (QD) and Three Times Weekly (TIW) for the Maintenance Treatment of Anemia ... | |||||||||||||||||||||||
Medical condition: Anemia of Chronic kidney disease (CKD) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) PL (Completed) CZ (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-004340-35 | Sponsor Protocol Number: CAMG-14-I | Start Date*: 2015-03-03 | |||||||||||
Sponsor Name:Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico | |||||||||||||
Full Title: Randomized controlled trial of two different combinations of Calcium-containing Phosphate binders (Ca-PiB) plus non-Calcium-non-Aluminum containing Phosphate binders (no-Ca-Al-PiB): a pharma-econom... | |||||||||||||
Medical condition: Hyperphosphatemia associated with Chronic Kidney Disease (CKD) in patients undergoing hemodialysis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002440-40 | Sponsor Protocol Number: TX200-KT03 | Start Date*: 2023-03-31 | |||||||||||
Sponsor Name:Sangamo Therapeutics France SAS | |||||||||||||
Full Title: Long-Term Follow-Up of Patients who have received an Autologous Antigen-Specific Chimeric Antigen Receptor T Regulatory Cell Therapy (CAR- Treg therapy, TX200-TR101) in a prior clinical study. | |||||||||||||
Medical condition: Prevention of immune mediated allograft rejection in patients with end-stage renal disease (ESRD) who are tissue typed as HLA-A*02 negative and have received a kidney transplant from an HLA-A*02 p... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) NL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002805-23 | Sponsor Protocol Number: 20120229(KAI-4169-006) | Start Date*: 2013-01-22 | ||||||||||||||||
Sponsor Name:KAI Pharmaceuticals, Inc (a subsidiary of Amgen, Inc.) | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Assess the Efficacy and Safety of AMG 416 in the Treatment of Secondary Hyperparathyroidism in Subjects With Chronic Kidney Disease ... | ||||||||||||||||||
Medical condition: Secondary hyperparathyroidism in subjects with chronic kidney disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) BE (Completed) CZ (Completed) GB (Completed) IT (Completed) DE (Completed) ES (Completed) AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003888-56 | Sponsor Protocol Number: 20192022 | Start Date*: 2021-01-30 | |||||||||||
Sponsor Name:Department of Nephrology, Herlev & Gentofte Hospital, Herlev Hospital | |||||||||||||
Full Title: Treatment of adynamic bone disorder with parathyroid hormone in patients with chronic kidney disease | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000081-13 | Sponsor Protocol Number: BA 17284 | Start Date*: 2004-09-07 |
Sponsor Name:F Hoffmann-La Roche Ltd | ||
Full Title: A randomized, controlled, open-label, multi-center, parallel group study to demonstrate efficacy and safety of RO0503821 when administered with pre-filled syringes for the maintenance treatment of ... | ||
Medical condition: Patients with Chronic Kidney Disease who are on dialysis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004032-75 | Sponsor Protocol Number: ML20572 | Start Date*: 2007-02-09 | |||||||||||
Sponsor Name:Roche Pharma AG | |||||||||||||
Full Title: An open-label, multi-center study to demonstrate the efficacy and safety of C.E.R.A when administered intravenously with pre-filled syringes (PFS) for the treatment of anemia in patients with chron... | |||||||||||||
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: 2017-001899-32 | Sponsor Protocol Number: RESINFENOL | Start Date*: 2017-08-17 |
Sponsor Name:Dr. Abelardo Aguilera Peralta | ||
Full Title: Crossover and randomized clinical trial on the effect of Resincolestiramine in the intestinal absorption of new uremic toxins in patients in hemodialysis with chronic renal insufficiency | ||
Medical condition: Chronic renal insufficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-002982-35 | Sponsor Protocol Number: Niaspan in CKD | Start Date*: 2005-11-21 |
Sponsor Name:Barts and The London NHS Trust | ||
Full Title: The effect of Niaspan (slow release nicotinic acid) on plasma phosphate, and renal phosphate handling in patents with severe chronic kidney disease | ||
Medical condition: Chronic renal failure (CKD stages 4 &%) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002475-35 | Sponsor Protocol Number: BO42353 | Start Date*: 2021-06-08 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE III, MULTICENTER, SINGLE-ARM STUDY EVALUATING THE EFFICACY, SAFETY, PHARMACOKINETICS, AND PHARMACODYNAMICS OF CROVALIMAB IN ADULT AND ADOLESCENT PATIENTS WITH ATYPICAL HEMOLYTIC UREMIC SYND... | |||||||||||||
Medical condition: Atypical Hemolytic Uremic Syndrome (aHUS) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) BE (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003527-14 | Sponsor Protocol Number: D9480C00023 | Start Date*: 2021-12-17 | |||||||||||
Sponsor Name:ASTRAZENECA AB | |||||||||||||
Full Title: An Open-Label, Randomised, Phase 4 Study of Continuing Sodium Zirconium Cyclosilicate (SZC) after Discharge in Participants with Chronic Kidney Disease treated for Hyperkalaemia | |||||||||||||
Medical condition: Patients with Chronic Kidney Disease treated for Hyperkalaemia whilst in hospital, who are normokalemic and established on maintenance dose of SZC at discharge. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Ongoing) FR (Completed) NL (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002437-15 | Sponsor Protocol Number: BO42354 | Start Date*: 2021-09-23 | |||||||||||
Sponsor Name:Roche Farma S. A. que realiza el ensayo en España y que actúa como representante F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE III, OPEN-LABEL, MULTICENTER, SINGLE-ARM STUDY EVALUATING THE EFFICACY AND SAFETY OF CROVALIMAB IN ADOLESCENT AND PEDIATRIC PATIENTS WITH ATYPICAL HEMOLYTIC UREMIC SYNDROME (aHUS) | |||||||||||||
Medical condition: Atypical Hemolytic Uremic Syndrome (aHUS) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) BE (Trial now transitioned) PL (Trial now transitioned) HU (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002270-52 | Sponsor Protocol Number: CIRIVA | Start Date*: 2013-12-05 | |||||||||||
Sponsor Name:Hospital Universitari de Girona Dr.Josep Trueta | |||||||||||||
Full Title: Effects of cinacalcet versus conventional treatment on metabolism bone and vascular involvement in advanced chronic renal failure | |||||||||||||
Medical condition: Bone's disorders and mineral metabolism and vascular involvement | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000676-13 | Sponsor Protocol Number: PRO-RENAL-REG-055 | Start Date*: 2004-11-19 | |||||||||||
Sponsor Name:Baxter Healthcare S.A. | |||||||||||||
Full Title: An Evaluation of the Efficacy of Epo-Omega in The Treatment of Anaemia in Chronic Kidney Disease (CKD) Patients When Administered by Once Weekly Subcutaneous Injection: A Dose Dependency Evaluation. | |||||||||||||
Medical condition: Anaemia in pre-dialysis Chronic Kidney Disease (CKD) Patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003972-21 | Sponsor Protocol Number: DS5565-A-U307 | Start Date*: 2015-09-10 | |||||||||||
Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED SAFETY STUDY OF DS-5565 FOR TREATMENT OF PAIN DUE TO FIBROMYALGIA IN SUBJECTS WITH CHRONIC KIDNEY DISEASE | |||||||||||||
Medical condition: DS-5565 is being investigated for the treatment of pain associated with fibromyalgia (FM) in subjects with chronic kidney disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) ES (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000179-13 | Sponsor Protocol Number: AG0/2006/001 | Start Date*: 2006-03-09 |
Sponsor Name:University Hospital Ghent | ||
Full Title: Validation of the methodology of serum creatinine measurement and the estimated glomular filtration ratio | ||
Medical condition: volunteers with different stage of renal disease or without renal disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003354-24 | Sponsor Protocol Number: 2013-NIGRAM-VUMC-001 | Start Date*: 2015-01-08 |
Sponsor Name:Vrij Universiteit Medical Center | ||
Full Title: Influence of exogenous growth hormone administration on circulating levels of Klotho in healthy and CKD subjects | ||
Medical condition: Cardiovascular disease in chronic kidney disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2025-000162-29 | Sponsor Protocol Number: D7413C00001 | Start Date*: 2025-08-27 |
Sponsor Name:Alexion Europe SAS | ||
Full Title: Prospective, Single-Arm, Multicenter Study to Evaluate the Efficacy, Safety, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Eculizumab in Complement Inhibitor Treatment-Naïve Pediatr... | ||
Medical condition: Atypical Hemolytic Uremic Syndrome (aHUS) | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
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