drugset / Trial / NCT00235300

An Open-label, Prospective, Randomized, Multi-center, Phase II Comparative Trial of Thymoglobulin Versus Simulect for the Prevention of Delayed Graft Function and Acute Allograft Rejection in Renal Allograft Recipients.

NCT00235300

Phase 2 Completed 240 enrolled Genzyme, a Sanofi Company
RandomizedParallel-groupOpen-labelPrevention

Summary

A multicenter clinical study comparing event-free survival at 6 months after transplant between Thymoglobulin-treated and Simulect-treated adult kidney transplant patients. Patients received Thymoglobulin or Simulect from Day 0 through Day 4. Day 0 was considered the day of the transplant procedure. Subjects meeting all inclusion and exclusion criteria were eligible to participate in this study. The treatment assignment was random and not chosen by the subject or their physician. Subjects were monitored during treatment with Thymoglobulin and during the transplant hospitalization. Additional subject monitoring occurred up to 12 months after transplant. 278 study subjects were enrolled at 28 transplant centers in the United States and Europe.

Timeline

Start
2000-05
Primary completion
2003-04
Completion
2005-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Basiliximab Monoclonal antibody 20 mg
Subject Thymoglobulin Protein / enzyme biologic 1.5 mg/kg