drugset / Trial / NCT00890253
Safety Study of Calcineurin-Inhibitor-Free Immunosuppression After Liver Transplantation
NaSingle-groupOpen-labelTreatment
Summary
A prospective, non-randomized two stage monocentric phase II clinical trial to evaluate a de-novo calcineurin-inhibitor (CNI)-free immunosuppressive regimen based on induction therapy with anti-CD25 monoclonal anti-body (basiliximab), mycophenolic acid (MPA), and mammalian target of rapamycin (mTOR) - inhibition with everolimus to determine its safety and to investigate the preliminary efficacy in patients with impaired renal function at the time-point of liver transplantation (OLT) with regards to the incidence of steroid resistant acute rejection within the first 30 days after liver transplantation.
Timeline
- Start
- 2010-01
- Primary completion
- 2012-01
- Completion
- 2013-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Basiliximab | Monoclonal antibody | 20 mg | Intravenous |
| Subject | Everolimus | Small molecule | 1 mg | Oral |
| Subject | Mycophenolate Sodium | Unknown | 1080 mg | Oral |
| Subject | Prednisolone | Other / unclassified | 7.5 mg | — |