- 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 1 of 34.
EudraCT Number: 2015-004459-38 | Sponsor Protocol Number: TREACE_2015 | Start Date*: 2016-02-24 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA INTEGRATA VERONA | ||||||||||||||||||
Full Title: EXPLORATIVE STUDY TO IDENTIFY A SPECIFIC TRANSCRIPTOMIC PROFILE FOR PREDICTING THE MAJOR ADVERSE EFFECTS ASSOCIATED WITH CERTICAN (EVEROLIMUS) IN RENAL TRANSPLANT RECIPIENTS: A PHARMACOGENOMIC APPR... | ||||||||||||||||||
Medical condition: kidney transplant | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004284-21 | Sponsor Protocol Number: 987 | Start Date*: 2007-07-06 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: A prospective randomized study of antibiotic prophylaxis for renal transplantation: short term vs standard treatment | |||||||||||||
Medical condition: antibiotic prophylaxis for renal tranplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003707-30 | Sponsor Protocol Number: P140501 | Start Date*: 2014-10-23 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000864-16 | Sponsor Protocol Number: CRAD001AIT02 | Start Date*: 2005-04-12 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: Multicenter, randomized, open-label trial to evaluate the safety, tolerability and efficacy of two regimens of Everolimus plus Neoral, given according different blood target levels, in de novo rena... | |||||||||||||
Medical condition: Prevention of rejection in adult renal transplant patients in combination with Neoral and corticosteroids | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000782-35 | Sponsor Protocol Number: CERL080AIT06 | Start Date*: 2004-06-10 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: EVALUATION OF THE QUALITY OF LIFE AND GASTROINTESTINAL SYMPTOMS AFTER CONVERSION TO MYFORTIC (ERL080) and CELLCEPT WITHDRAWAL IN MAINTENANCE RENAL TRANSPLANT RECIPIENTS TREATED WITH TACROLIMUS. | |||||||||||||
Medical condition: Prophylaxis of transplant rejection in adult patients receiving calcineurin inhibitors with / without corticosteroids after allogeneic renal transplants. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006729-15 | Sponsor Protocol Number: IGG-GIFA-001 | Start Date*: 2008-11-25 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: OPEN PILOT STUDY, TWO ARMS, WITH HISTORIC CONTROL, MULTICENTRIC TO EVALUATE SAFETY AND EFFICACY OF ASSOCIATION WITH EVEROLIMUS AND LOW DOSES OF CYCLOSPORIN AND STEROIDS AFTER INDUCTION WITH MONOCLO... | |||||||||||||
Medical condition: pediatric patient after kidney transplant | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000655-41 | Sponsor Protocol Number: CFTY720A2308 | Start Date*: 2005-02-10 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A | |||||||||||||
Full Title: A one-year, multicenter, open-label, feasibility study to evaluate the safety and the efficacy of FTY720 5mg introduction and CNI elimination in adult maintenance renal transplant reicpients mainta... | |||||||||||||
Medical condition: prevention of acute rejection in maintenance renal transplant recipients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006072-30 | Sponsor Protocol Number: 0808100 | Start Date*: 2009-01-19 | ||||||||||||||||
Sponsor Name:CHU Saint-Etienne | ||||||||||||||||||
Full Title: Mycophénolate sodic in graded increased doses in the first 3 months of renal transplantation _ Pharmacokinetic descriptive Pilot study | ||||||||||||||||||
Medical condition: renal transplantation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012350-20 | Sponsor Protocol Number: MSC-KTx | Start Date*: 2008-01-14 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: MESENCHYMAL STEM CELLS UNDER BASILIXIMAB/ LOW DOSE RATG TO INDUCE RENAL TRANSPLANT TOLERANCE | |||||||||||||
Medical condition: Patients will be those receiving a living-related kidney transplant | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007047-13 | Sponsor Protocol Number: TER_AFE2009 | Start Date*: 2009-04-27 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: Prevention and treatment of kidney transplantation rejection by means of innovative therapeutic apheresis. | |||||||||||||
Medical condition: Patients waiting for first corpse kidney transplantation or re-transplantation, with PRA values > 50% | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000771-42 | Sponsor Protocol Number: CRAD001ASE01 | Start Date*: 2007-10-20 | |||||||||||
Sponsor Name:Novartis Pharma Services | |||||||||||||
Full Title: A controlled randomized open-label multicentre study evaluatiing if early conversion to everolimus (Certican) from cyclosporine (Neoral) in de novo renal transplant receipients can improve long-ter... | |||||||||||||
Medical condition: Renal Transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004158-33 | Sponsor Protocol Number: CYP3A4/5+PGPinRenalTx | Start Date*: 2008-09-17 | |||||||||||
Sponsor Name:Department of Nephrology and Renal Transplantation, KU Leuven | |||||||||||||
Full Title: CYP3A4/5 and PGP activity in renal transplantation. A study assessing in vivo hepatic and intestinal CYP3A4/5 and PGP activity in kidney transplant recipients and its relationship with genetic and... | |||||||||||||
Medical condition: Effect of genetic (single nucleotide polymorphisms of genes encoding drug metabolising enzymes and drug transporters) and non-genetic factors (e.g. age, time after transplantation, concommitant med... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002856-17 | Sponsor Protocol Number: SMHREN0501 | Start Date*: 2006-12-28 | |||||||||||
Sponsor Name:Hammersmith Hospital NHS Trust | |||||||||||||
Full Title: A randomised controlled comparison of Campath−Tacrolimus vs IL2R MoAb −Tacrolimus / Mycophenolate as Induction−Maintenance immunosuppression in kidney transplantation. | |||||||||||||
Medical condition: Renal transplant failure and rejection (Live and deceased donor) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001144-23 | Sponsor Protocol Number: CERL080ADE10 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: Measurement of Patient Reported Gastrointestinal (GI) and Health-related Quality of Life (HRQL) Outcomes in Simultaneous Pancreas-Kidney Transplant Recipients | |||||||||||||
Medical condition: Stable Pancreas-Kidney (SPK) Transplant Recipients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004069-16 | Sponsor Protocol Number: CYP3A4/5RenalTx | Start Date*: 2007-10-19 | |||||||||||
Sponsor Name:Department of Nephrology and Renal Transplantation, KU Leuven | |||||||||||||
Full Title: Hepatic and intestinal CYP3A4/5 activity in renal transplantation. A study assessing in vivo hepatic and intestinal CYP3A4/5 activity at different time-points and in different clinical settings af... | |||||||||||||
Medical condition: Effect of genetic (single nucleotide polymorphisms of genes encoding drug metabolising enzymes and drug transporters) and non-genetic factors (e.g. age, time after transplantation, concommitant me... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019126-13 | Sponsor Protocol Number: CE-US | Start Date*: 2011-03-04 | |||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
Full Title: A PILOT, EXPLORATIVE STUDY TO IDENTIFY CONTRAST-ENHANCED ULTRASOUND (CE-US) PATTERNS THAT CHARACTERIZE ACUTE ALLOGRAFT REJECTION AND OTHER CAUSES OF ACUTE ALLOGRAFT DYSFUNCTION IN RENAL TRANSPLANT ... | |||||||||||||
Medical condition: Renal transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013461-25 | Sponsor Protocol Number: UK-02-RG-194_09.0098 | Start Date*: 2010-03-03 | |||||||||||
Sponsor Name:St. George's, University of London | |||||||||||||
Full Title: The influence of CYP3A5 and ABCB1 genotype on the pharmacokinetics of twice daily Tacrolimus and Advagraf | |||||||||||||
Medical condition: Renal transplantation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014670-17 | Sponsor Protocol Number: CORPAD | Start Date*: 2009-12-07 | |||||||||||
Sponsor Name:H.-Hartziekenhuis Roeselare-Menen vzw | |||||||||||||
Full Title: Controlled study on the Relative Pharmacokinetics of Advagraf versus Prograft in Kidney transplant patients with severe Diarrhoea | |||||||||||||
Medical condition: Renal transplant patients suffering from diarrhea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000033-19 | Sponsor Protocol Number: 4xmmf | Start Date*: 2007-06-05 | |||||||||||||||||||||
Sponsor Name:UMC Utrecht | |||||||||||||||||||||||
Full Title: An open study to investigate the effect of 4 instead of 2 daily dosing mycophenolate mofetil (MMF) in renal transplant patients on diarrhea | |||||||||||||||||||||||
Medical condition: Diarrhea in renal transplanted patients which use Cellcept® | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005604-14 | Sponsor Protocol Number: AIFA TX | Start Date*: 2006-12-19 | |||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
Full Title: A randomized, prospective, multicenter trial to compare the effect on chronic allograft nephropathy prevention of mycophenolate mofetil versus azathioprine as the sole immunosuppressive therapy f... | |||||||||||||
Medical condition: kidney transplant | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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