- 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 5 of 34.
EudraCT Number: 2021-002640-70 | Sponsor Protocol Number: 20-HMedIdeS-19 | Start Date*: 2022-04-13 | |||||||||||
Sponsor Name:Hansa Biopharma AB | |||||||||||||
Full Title: A controlled, open-label post-authorisation efficacy and safety study in imlifidase desensitised kidney transplant patients with positive crossmatch against a deceased donor prior to imlifidase tre... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) AT (Trial now transitioned) BE (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) SI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005503-13 | Sponsor Protocol Number: 1.0_Custodiol | Start Date*: 2015-02-16 | |||||||||||
Sponsor Name:Essen University Hospital, University of Essen, Klinik für Allgemein-, Viszeral- und Transplantationschirugie | |||||||||||||
Full Title: A prospective randomized single blind monocenter phase II study of organ perfusion with Custodiol-N compared with Custodiol solution in living donor kidney transplantation | |||||||||||||
Medical condition: kidney preservation by Custodiol-N or Custodiol solution before living related kidney transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001183-31 | Sponsor Protocol Number: MT18328 | Start Date*: 2005-10-20 |
Sponsor Name:F. Hoffmann-La Roche Ltd | ||
Full Title: A prospective, open label, randomized, multicenter, multinational study evaluating the overall efficacy and safety including the effect on renal function of sirolimus (Rapamune) replacing CNI in a... | ||
Medical condition: Heart Transplant | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) AT (Completed) CZ (Completed) GB (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001101-22 | Sponsor Protocol Number: PURE | Start Date*: 2021-08-23 | |||||||||||
Sponsor Name:Amsterdam UMC | |||||||||||||
Full Title: Study to evaluate the efficacy and side effects of Envarsus in patients who had a kidney transplantation | |||||||||||||
Medical condition: Kidney transplant immunosupression for patients with CYP3A5*1 gene variance | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004956-39 | Sponsor Protocol Number: SMART-DSA | Start Date*: 2014-06-18 | |||||||||||
Sponsor Name:Klinikum der Universität München | |||||||||||||
Full Title: Study to evaluate the impact of donor-specific HLA-antibodies on graft function and survival after renal transplantation - Long term follow up of the SMART study population | |||||||||||||
Medical condition: Renal Transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002914-20 | Sponsor Protocol Number: RRK3367 | Start Date*: 2007-09-20 | ||||||||||||||||
Sponsor Name:University Hospital Birmingham NHS Foundation Trust | ||||||||||||||||||
Full Title: Calcineurin Inhibitor Minimisation in Renal Transplant Recipients with Stable Allograft Function: A Prospective Randomised Controlled Trial | ||||||||||||||||||
Medical condition: Renal Transplantation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000796-32 | Sponsor Protocol Number: 185/13 | Start Date*: 2014-01-28 | |||||||||||
Sponsor Name:Policlinico A. Gemelli | |||||||||||||
Full Title: A multiple centre, randomised, open label, prospective clinical study to compare the efficacy and safety of a combination of tacrolimus with everolimus versus the combination of tacrolimus with MM... | |||||||||||||
Medical condition: KIDNEY TRANSPLANTATION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004947-23 | Sponsor Protocol Number: none | Start Date*: 2006-02-22 |
Sponsor Name:UF de méthodologie en recherche clinique | ||
Full Title: Efficacité de la rapamycine dans la prévention secondaire des cancers cutanés chez les transplantés rénaux. Etude ouverte randomisée Rapamycine vs anticalcineurines | ||
Medical condition: To evaluate the impact of two imnosupressive regimens on the incidence of skin cancers among patients who has a first spinocellular skin cancer after renal transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004346-40 | Sponsor Protocol Number: CRAD001A2418 | Start Date*: 2005-05-02 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: Full title of the trial : Multi-center, open-label, prospective, randomized, parallel group study investigating a CNI-free regimen with Myfortic® and Certican® in comparison to standard therapy wit... | |||||||||||||
Medical condition: de novo kidney transplantation (cadaveric, living unrelated or living related) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017066-23 | Sponsor Protocol Number: RituxiRT | Start Date*: 2010-01-25 | |||||||||||
Sponsor Name:Guys and St Thomas Foundation Trust | |||||||||||||
Full Title: A randomized trial of Rituximab in induction therapy for living donor renal transplantation | |||||||||||||
Medical condition: End stage renal disease; renal function after renal transplantation | |||||||||||||
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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) |
EudraCT Number: 2018-000131-27 | Sponsor Protocol Number: AC17065 | Start Date*: 2018-05-23 | |||||||||||
Sponsor Name:University of Edinburgh [...] | |||||||||||||
Full Title: Heme arginate in transplantation - a multi-centre blinded parallel-group randomised trial of heme arginate versus placebo to reduce delayed graft function in kidney transplant recipients. (The HOT ... | |||||||||||||
Medical condition: End stage renal disease patients undergoing a deceased donor kidney transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004377-28 | Sponsor Protocol Number: CFTY720A0124E1 | Start Date*: 2005-02-03 | |||||||||||
Sponsor Name:Novartis Pharma 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: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003298-24 | Sponsor Protocol Number: EVITAESTEROIDE-12 | Start Date*: 2014-06-26 | |||||||||||
Sponsor Name:Sociedad Andaluza de Trasplante de Órganos y Tejidos (SATOT) | |||||||||||||
Full Title: Steroid withdrawal and novo donor-specific anti-HLA antibodies in renal transplant patients: a prospective, randomized and controlled study in parallel groups. | |||||||||||||
Medical condition: Kidney transplantaion | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004302-10 | Sponsor Protocol Number: Intercept | Start Date*: 2020-08-19 | |||||||||||
Sponsor Name:Västra Götalandsregionen, Sahlgrenska University hospital | |||||||||||||
Full Title: A randomized controlled open-label multi-center study to assess the efficacy of Tocilizumab in treatment of chronic active antibody-mediated rejection in kidney transplant recipients | |||||||||||||
Medical condition: Treatment of chronic active antibody-mediated rejection in kidney transplant recipients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004101-33 | Sponsor Protocol Number: 0468E-102362 | Start Date*: 2015-04-07 | |||||||||||
Sponsor Name:Wyeth Korea, Inc. | |||||||||||||
Full Title: A Clinical Study to Evaluate the Efficacy and Safety of Cyclosporine (CsA) and Sirolimus (SRL) Induction Followed by Cyclosporine Withdrawal in Korean Renal Allograft Recipients | |||||||||||||
Medical condition: Renal transplantation | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000531-18 | Sponsor Protocol Number: CAEB071A2206E1 | Start Date*: 2008-10-10 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 24-month extension to a 12-month, open-label, randomised, multicenter, sequential cohort, dose finding study to evaluate the efficacy, safety and tolerability of oral AEB071 versus Neoral® in com... | |||||||||||||
Medical condition: To provide continued treatment and to assess the long term safety, efficacy and tolerability of oral AEB071 plus Certican® vs. Neoral® plus Certican® in de novo renal transplant recipients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) AT (Prematurely Ended) NL (Prematurely Ended) CZ (Completed) BE (Prematurely Ended) IT (Prematurely Ended) ES (Completed) SK (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003231-20 | Sponsor Protocol Number: BE-02-RG-186 | Start Date*: 2008-11-26 | |||||||||||
Sponsor Name:KULeuven | |||||||||||||
Full Title: Adherence Measurement in stable renal transplant patients following conversion form Prograft to advagraf | |||||||||||||
Medical condition: Renal transplant patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004102-15 | Sponsor Protocol Number: 0468H-102012 | Start Date*: 2015-04-06 | |||||||||||
Sponsor Name:Wyeth | |||||||||||||
Full Title: An open label comparative study of de novo renal allograft recipients receiving CsA + MMF + corticosteroids versus CsA + Rapamune + corticosteroids with further CsA elimination in the Rapamune ar... | |||||||||||||
Medical condition: Renal Transplantation | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004771-22 | Sponsor Protocol Number: Vs.12.11-07-2008 | Start Date*: 2008-09-03 | |||||||||||||||||||||
Sponsor Name:Rigshospitalet, Kardiologisk afd | |||||||||||||||||||||||
Full Title: Prospective randomised dubbleblind placebocontrolled trial of calcium antagonist to prevent calcineurin induced nephropathy in lung transplanted patients | |||||||||||||||||||||||
Medical condition: kidney damage in ciclosporin treated lung transplant patients. | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014830-10 | Sponsor Protocol Number: GCPD_27july09 | Start Date*: 2009-11-04 |
Sponsor Name:Medizinische Universität Wien, Univ.Klinik Innere Medizin III, Abt.für Nephrologie u.Dialyse | ||
Full Title: Glucose Control in Pre-Diabetic Renal Transplant Patients: Efficacy and Safety of Vildagliptin and Pioglitazone | ||
Medical condition: new onset diabetes mellitus after transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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