Heart Spare the Nephron (STN) Study - A Study of CellCept (Mycophenolate Mofetil) and Rapamune (Sirolimus) in Heart Transplant Recipients
| Status: | Terminated |
|---|---|
| Conditions: | Cardiology |
| Therapuetic Areas: | Cardiology / Vascular Diseases |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 8/3/2016 |
| Start Date: | October 2005 |
| End Date: | August 2006 |
A Randomized, Open-label Study of the Effect of Replacing CNI With Sirolimus in a Standard Care Regimen of CNI, CellCept, and Steroids on Renal Function in Heart Transplant Patients
Heart transplant patients on a standard care regimen of CNI, MMF, and corticosteroids will
enter the study 4-6 weeks post-transplant. At 3 months after transplant, patients will be
randomized to either continue this regimen or CNI therapy will be discontinued and replaced
by sirolimus therapy (in combination with MMF and corticosteroids). The effect of these 2
regimens on efficacy, safety and renal function will be evaluated.The anticipated time on
study treatment is 1-2 years and the target sample size is 500+ individuals.
enter the study 4-6 weeks post-transplant. At 3 months after transplant, patients will be
randomized to either continue this regimen or CNI therapy will be discontinued and replaced
by sirolimus therapy (in combination with MMF and corticosteroids). The effect of these 2
regimens on efficacy, safety and renal function will be evaluated.The anticipated time on
study treatment is 1-2 years and the target sample size is 500+ individuals.
Inclusion Criteria:
- adult (>=18 years of age) heart transplant patients (4-6 weeks post-transplant);
- receipt of first heart (single-organ) transplant;
- standard care regimen of CNI, MMF, and corticosteroids since transplantation.
Exclusion Criteria:
- positive donor-specific cross-match at time of transplantation;
- history of malignancies, other than non-melanoma skin cancer that has been totally
excised with no recurrence for 2 years;
- patients participating in another interventional clinical trial or requiring
treatment with unmarketed investigational drugs.
We found this trial at
12
sites
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