276
Participants
Start Date
August 31, 2006
Primary Completion Date
January 31, 2013
Study Completion Date
January 31, 2013
everolimus
Start dose of everolimus was 1.5 mg in the morning followed by 1.5 mg in the evening. After one week, the dose was adjusted to achieve trough levels between 5-12 ng/mL. Once trough levels were above 5ng/mL, the CNI dose was reduced to 70%. At week 8 post-baseline (latest at week 16 post baseline), CNI was completely discontinued. For patients receiving Ciclosporin A (CiA) as CNI, the everolimus dosage was adjusted to achieve a trough level of 8-12 ng/mL, prior to discontinuation of CiA. After discontinuation of CNI, everolimus was maintained at a trough level of 5-12 ng/mL.
basiliximab
All patients who met the eligibility criteria were treated with 2 doses of basiliximab on Day 0 (transplantation) and Day 4.
CNI
Patients who met the screening eligibility received CNI-based immunosuppressive therapy for 1 month. Then at week 4 (or week 8 at maximum), patients randomized to the CNI arm continued on CNI-based immunosuppressive therapy.
Novartis Investigative Site, Geneva
Novartis Investigative Site, Zurich
Novartis Investigative Site, Berlin
Novartis Investigative Site, Hamburg
Novartis Investigative Site, Hanover
Novartis Investigative Site, Essen
Novartis Investigative Site, Münster
Novartis Investigative Site, Frankfurt
Novartis Investigative Site, Heidelberg
Novartis Investigative Site, Tübingen
Novartis Investigative Site, Regensburg
Novartis Investigative Site, Innsbruck
Novartis Investigative Site, Vienna
Novartis Investigative Site, Jena
Novartis Investigative Site, Groningen
Novartis Investigative Site, Rotterdam
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY