drugset / Trial / NCT00928811

Study to Evaluate the Safety of Chronic Administration of Simulect to Subjects Receiving a First Kidney Transplant

NCT00928811

RandomizedParallel-groupOpen-labelTreatment

Summary

The study is undertaken to explore the safety of using Simulect at monthly dose intervals to reduce the need of high dose/level CNI's such as Prograf.

Timeline

Start
2009-05
Primary completion
2010-04
Completion
2010-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Basiliximab Monoclonal antibody 20 mg Intravenous
Subject Basiliximab Monoclonal antibody 40 mg Intravenous