696
Participants
Start Date
May 7, 2003
Primary Completion Date
September 19, 2005
Study Completion Date
September 19, 2005
FTY720 5 mg + reduced-dose Neoral (RDN) + corticosteroids
FTY720 5 mg + reduced-dose Neoral (RDN) + corticosteroids
FTY720 2.5 mg + full dose Neoral (FDN) + corticosteroids
FTY720 2.5 mg + full dose Neoral (FDN) + corticosteroids
MMF 2 g + full-dose Neoral (FDN) + corticosteroids
mycophenolate mofetil (MMF) + full-dose Neoral (FDN) + corticosteroids
Hawthorne
Philadelphia
Fairfax
Richmond
Chapel Hill
Durham
Charleston
Atlanta
Atlanta
Augusta
Tampa
Nashville
Memphis
Toledo
Cleveland
Cleveland
Indianapolis
Ann Arbor
Detroit
Des Moines
Milwaukee
Madison
Minneapolis
Rochester
Chicago
Omaha
Dallas
Houston
Galveston
San Antonio
Denver
Salt Lake City
Phoenix
Los Angeles
San Francisco
Palo Alto
Portland
New Haven
Portland
Boston
Boston
Livingston
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY