Everolimus Versus Mycophenolate Mofetil in Combination With Reduced Dose Cyclosporine Microemulsion in Maintenance Heart Transplant Recipients
NCT00170859 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL
Last updated 2016-11-18
Summary
In this study two immunosuppressive regimens (everolimus in combination with cyclosporine microemulsion and mycophenolate mofetil with cyclosporine microemulsion) with reduced dose cyclosporine microemulsion are compared in maintenance heart transplant recipients with impaired renal function.
Conditions
- Heart Transplantation
Interventions
- DRUG
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Novartis · Novartis
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2004-08-31
- Primary Completion
- 2006-11-30
- Completion
- 2006-12-31
Countries
- Germany
More Related Trials
-
Efficacy and Safety of Everolimus With Enteric-Coated Mycophenolate Sodium (EC-MPS) in a Cyclosporine Microemulsion-free Regimen Compared to Standard Therapy in de Novo Renal Transplant Patients
NCT00154310 ·Status: COMPLETED ·Phase: PHASE4
-
Everolimus in de Novo Heart Transplant Recipients
NCT01017029 ·Status: COMPLETED ·Phase: PHASE4
-
Non-inferiority Study of Safety and Efficacy of Everolimus With Low Dose Tacrolimus to Mycophenolate Mofetil With Standard Dose Tacrolimus in Kidney Transplant Recipients
NCT01025817 ·Status: COMPLETED ·Phase: PHASE3
-
Everolimus and Low Dose CNI Compared With MMF and Full CNI Dose in Heart Transplanted Patients: One Year Follow up
NCT00596557 ·Status: COMPLETED ·Phase: PHASE4
-
Pharmacokinetics of Everolimus and Enteric-Coated Mycophenolatesodium Before and After Withdrawal of Cyclosporine in Renal Transplant Patients
NCT00443937 ·Status: COMPLETED ·Phase: PHASE4
-
Study to Evaluate Effect of Everolimus in Progression of Graft Vascular Illness on Patients With Heart Transplant
NCT00695344 ·Status: UNKNOWN ·Phase: PHASE4
-
Study of the Effect of Everolimus Immunosuppressive Combination Therapies on Renal Function When Used as a Maintenance Treatment for Liver Transplant Patients.
NCT03596970 ·Status: WITHDRAWN ·Phase: PHASE3
-
Efficacy and Safety of Everolimus in Combination With Cyclosporine Microemulsion Versus Everolimus in Combination With Enteric-coated Mycophenolate Sodium (EC-MPS), in Adult Renal Transplant Patients in Maintenance.
NCT00425308 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of Everolimus+EC-MPS After Early CNI Elimination vs EC-MPS +Tacrolimus in Renal Transplant Recipients
NCT00965094 ·Status: COMPLETED ·Phase: PHASE4
-
Everolimus in Combination With Cyclosporine Microemulsion in de Novo Renal Transplant Recipients
NCT01276457 ·Status: COMPLETED ·Phase: PHASE3
-
24 Months Follow-up, Two Arm Study to Compare the Cardiovascular Profile in a Regimen With Everolimus + Mycophenolic Acid (MPA) Versus (vs.) a Regimen of CNI+MPA in Maintenance Renal Transplant Recipients
NCT01169701 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of AEB071 Plus Tacrolimus (Converted to Mycophenolic Acid After 3 Months), in Renal Transplant Patients
NCT00403416 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Evaluation of Early Conversion to Everolimus From Cyclosporine in de Novo Renal Transplant Recipients
NCT00634920 ·Status: COMPLETED ·Phase: PHASE4
-
Optimize Immunosuppressive Therapy Using Everolimus and Low-dose Calcineurin Inhibitors in Heart Transplant Patients in Korea
NCT06942156 ·Status: NOT_YET_RECRUITING ·Phase: PHASE4
-
Efficacy and Tolerability of Full Dose Enteric-coated Mycophenolate Sodium, in Addition to Cyclosporine for Microemulsion Reduced Dose, in Maintenance Renal Transplant Recipients
NCT00434590 ·Status: TERMINATED ·Phase: PHASE4
-
Efficacy and Safety Study of Everolimus Plus Reduced Cyclosporine Versus Mycophenolic Acid Plus Cyclosporine in Kidney Transplant Recipients
NCT00251004 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of the Switch From Sirolimus to Everolimus in Stable Maintenance Renal Transplant Patients Receiving a Calcineurin Inhibitor Free Regimen
NCT00170820 ·Status: COMPLETED ·Phase: PHASE4
-
Safety/Efficacy of Everolimus and Neoral® in Adult Cardiac Transplant Patients With Established Allograft Vasculopathy
NCT00097968 ·Status: COMPLETED ·Phase: PHASE3
-
Comparison of CNI-based Regimen Versus CNI-free Regimen in Kidney Transplant Recipients.
NCT00332839 ·Status: TERMINATED ·Phase: PHASE4
-
Proportion of CMV Seropositive Kidney Transplant Recipients Who Will Develop a CMV Infection When Treated With an Immunosuppressive Regimen Including Everolimus and Reduced Dose of Cyclosporine Versus an Immunosuppressive Regimen With Mycophenolic Acid and Standard Dose of Cyclosporine A
NCT02328963 ·Status: COMPLETED ·Phase: PHASE4
-
Everolimus in a Cyclosporine Microemulsion-free Regimen Compared to a Low-dose Cyclosporine Microemulsion Regimen, in de Novo Kidney Transplant Patients
NCT00154284 ·Status: COMPLETED ·Phase: PHASE3
-
12 Month Athena Study: Everolimus vs. Standard Regimen in de Novo Kidney Transplant Patients
NCT01843348 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of Enteric-Coated Mycophenolate Sodium (EC-MPS) in Renal Transplant Patients
NCT00239083 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy of Everolimus in Combination With Tacrolimus in Liver Transplant Recipients
NCT01551212 ·Status: COMPLETED ·Phase: PHASE4
-
A National Multi-center Randomized, Open Label Study to Evaluate Efficacy and Safety of Everolimus With EC-MPS Compared to Standard Treatment Combination Tacrolimus and EC-MPS in de Novo Liver Transplant Recipients
NCT01625377 ·Status: COMPLETED ·Phase: PHASE3