- Trials with a EudraCT protocol (676)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (31)
676 result(s) found for: Renal transplant.
Displaying page 3 of 34.
EudraCT Number: 2004-004958-63 | Sponsor Protocol Number: CFTY720 0125E1 | Start Date*: 2005-08-04 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A two-year extension to a one-year, multicenter, partially blinded, double-dummy, randomized study to evaluate the efficacy and safety of FTY720 combined with reduced-dose or full-dose Neoral and c... | |||||||||||||
Medical condition: Prophylaxis of kidney allograft rejection in de novo adult renal transplant recipients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004695-20 | Sponsor Protocol Number: ML19313 | Start Date*: 2006-03-27 | |||||||||||
Sponsor Name:Roche Pharma AG | |||||||||||||
Full Title: Randomized multicenter trial comparing Valganciclovir CMV prophylaxis versus pre-emptive therapy after renal transplantation using proteomics for monitoring of graft alteration | |||||||||||||
Medical condition: Prevention of cytomegalovirus (CMV) disease in kidney transplant recipients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021275-92 | Sponsor Protocol Number: CERL080ADE20T | Start Date*: 2010-09-16 | |||||||||||||||||||||
Sponsor Name:Charité – Universitätsmedizin Berlin | |||||||||||||||||||||||
Full Title: Single center, open-label, cross-over study in maintenace kidney allograft recipients to evaluate the bioavailability of CellCept® (Mycophenolate mofetil) in comparison to Myfortic® (Enteric- coate... | |||||||||||||||||||||||
Medical condition: Prophylaxis against renal transplant rejection Renal transplant -> immunosuppressant drug therapy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-004558-44 | Sponsor Protocol Number: 2021-00604 | Start Date*: 2021-10-10 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:UMCG | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Optimal Booster Strategy for SARS-CoV-2 Vaccination in Kidney Transplant patients | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: COVID-19 is associated with severely increased morbidity and mortality in kidney transplant patients. Available data show that the immune response after a standard regimen of two mRNA vaccinations ... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002594-28 | Sponsor Protocol Number: APHP200036 | Start Date*: 2022-10-05 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Graft Acute kidney injury: vitamin B3 to facilitate renal Recovery In the Early Life of a transplant | |||||||||||||
Medical condition: Patients with end-stage renal failure treated with extrarenal purification (hemodialysis using a catheter or a fistula, or peritoneal dialysis), registered on the national kidney donation waiting l... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001518-42 | Sponsor Protocol Number: CERL080A2409 | Start Date*: 2005-09-15 | |||||||||||
Sponsor Name:Novartis Farmaceútica S.A | |||||||||||||
Full Title: A six-month, prospective, multicenter, open label, parallel, randomized study of the safety, tolerability and efficacy of myfortic® (ERL080) with Simulect®, corticosteroids and two different levels... | |||||||||||||
Medical condition: de novo renal transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000855-14 | Sponsor Protocol Number: 01-865-2005 | Start Date*: 2005-07-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA | |||||||||||||
Full Title: Multicenter, not controlled, prospectic clinical phase IV study: safety and efficacy of an immunosuppressive regimen with Thymoglobuline and Rapamune in patients receiving a renal transplantation f... | |||||||||||||
Medical condition: Acute rejection prophylaxis after single-double kidney transplantation from marginal donors making use of a not nephrotoxic immunosuppressive regimen. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000237-12 | Sponsor Protocol Number: IM103-402 | Start Date*: 2021-05-04 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Prospective, Open-label, Multicenter, Randomized Study to Evaluate the Benefits and Risks of Conversion of Existing Adolescent Renal Allograft Recipients Aged 12 to Less Than 18 Years of Age to a... | |||||||||||||
Medical condition: Adolescent Renal Allografts | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001806-94 | Sponsor Protocol Number: VACC-IR | Start Date*: 2006-05-22 |
Sponsor Name:Hôpital Erasme | ||
Full Title: Comparison of the efficacy of pneumococcal and tetanus vaccination between hemodialysis patients and renal tranpslant recipients treated with Mycophenolic acid(VACC-IR) study. | ||
Medical condition: Patients on dialysis and waiting for renal transplant and renal translanted patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004934-14 | Sponsor Protocol Number: EMASPK01 | Start Date*: 2014-01-15 | ||||||||||||||||
Sponsor Name:Institut klinické a experimentální medicíny | ||||||||||||||||||
Full Title: EVEROLIMUS VERSUS MYCOPHENOLIC ACID IN SIMULTANEOUS PANCREAS AND KIDNEY TRANSPLANTATION TO EVALUATE THE DIFFERENCES IN RETINAL NEOVASCULARIZATION IN PATIENTS WITH DIABETIC RETINOPATHY | ||||||||||||||||||
Medical condition: simultaneous pancreas/kidney allograft transplantation | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000822-38 | Sponsor Protocol Number: COSTANT | Start Date*: 2008-06-12 | |||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
Full Title: A PROSPECTIVE, RANDOMIZED, OPEN LABEL BLINDED END POINT (PROBE), CROSS-OVER STUDY TO COMPARE THE EFFECTS OF TELMISARTAN AND LOSARTAN ON METABOLIC PROFILE OF RENAL TRANSPLANT PATIENTS | |||||||||||||
Medical condition: kidney transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012200-98 | Sponsor Protocol Number: yCAN | Start Date*: 2011-01-21 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: Open-label, prospective, randomized, parallel group study investigating a CNI-low dose regimen with Sandimmun® Optoral and Certican® in comparison to standard immunosuppressive therapy in renal tra... | |||||||||||||
Medical condition: Maintenance outpatient renal transplant recipients at least 6 months post-transplantation, no longer than 8 years after transplantation with a creeping serum creatinine (as calculated by CAN-Slope®... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002328-40 | Sponsor Protocol Number: HHSC/005 | Start Date*: 2007-05-18 | ||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||
Full Title: A phase I safety and tolerability study of infusing the autologous progeny of an adult CD34+ subset into patients with type I diabetes mellitus and a successful renal transplant. | ||||||||||||||||||
Medical condition: Diabetes mellitus type 1 and succesful renal transplant | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002807-21 | Sponsor Protocol Number: VitaD-1 | Start Date*: 2008-10-15 | ||||||||||||||||
Sponsor Name:MUW, Universitätsklinik für Innere Medizin III, Abteilung für Nephrologie und Dialyse | ||||||||||||||||||
Full Title: VITA-D: Cholecalciferol substitution in vitamin D deficient kidney transplant recipients: A randomized, placebo-controlled study to evaluate the posttransplant outcome | ||||||||||||||||||
Medical condition: Vitamin D deficiency in kidney transplant recipients | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000726-11 | Sponsor Protocol Number: SHP616-302 | Start Date*: 2016-03-08 | |||||||||||
Sponsor Name:Shire Viropharma, Inc. | |||||||||||||
Full Title: A randomized double-blind placebo-controlled study to evaluate the efficacy and safety of Cinryze® (C1 esterase inhibitor [human]) for the treatment of acute antibody-mediated rejection in kidney t... | |||||||||||||
Medical condition: Acute Antibody Mediated Rejection (AMR) in kidney transplant patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000718-52 | Sponsor Protocol Number: DMPT-17 | Start Date*: 2017-05-09 |
Sponsor Name:Hospital Universitario de Canarias | ||
Full Title: Efficacy of a new formulation of a daily lctp dose of tacrolimus (ENVARSUS®) to prevent diabetes post renal transplant in patients at risk: a controlled randomized open pilot study | ||
Medical condition: diabetes post-renal trasnplant | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2005-006162-33 | Sponsor Protocol Number: ML 19835 | Start Date*: 2006-07-03 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Relationships between pharmacokinetic and pharmacodynamic strategies for assessment of the risks for acute rejection and side effects of mofetil mycophenolate | |||||||||||||
Medical condition: Kidney transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002866-19 | Sponsor Protocol Number: CRAD001AIT25 | Start Date*: 2011-07-25 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A 3-month, multicenter, randomized, open label study to evaluate the impact of early vs delayed introductioN of EVERolimus on WOUND healing in de novo kidney transplant recipients (NEVERWOUND study) | |||||||||||||
Medical condition: Renal transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000380-26 | Sponsor Protocol Number: CERTES02 (Ce-PoP-RAD001A2419) | Start Date*: 2005-05-24 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A. | |||||||||||||
Full Title: A 12 month, multicenter, randomized, parallel, open-label study, to evaluate renal function and efficacy of Certican® (everolimus) with Simulect® (basiliximab) and cyclosporine discontinuation at 3... | |||||||||||||
Medical condition: Renal Transplant | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000868-30 | Sponsor Protocol Number: NL76215.042.20 | Start Date*: 2021-02-17 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:RECOVAC consortium | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: The immune-response and safety of COVID-19 vaccination in patients with chronic kidney disease, on dialysis, or living with a kidney transplant | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: COVID-19 is associated with increased morbidity and mortality in kidney transplant recipients (KTR) and patients with chronic kidneydisease (CKD). Therefore, potential efficacious SARS-CoV-2 vaccin... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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