drugset / Trial / NCT01336296
Evaluate Effects and Safety of Pre-load Myfortic® in Transplant Patients
RandomizedParallel-groupOpen-labelTreatment
Summary
This study is specifically designed to determine whether the initiation of Myfortic 2 weeks prior to transplantation will enhance the therapeutic efficacy of Simulect induction therapy in low to moderate risk patients. Specifically, the addition of Myfortic pretransplant to Simulect induction will be compared to standard Myfortic therapy with Thymoglobulin induction starting at the time of transplant in kidney transplant recipients.
Timeline
- Start
- 2010-09
- Primary completion
- 2014-04
- Completion
- 2014-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | mycophenolic acid | Small molecule | 720 mg | Oral |