Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/35704
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dc.contributor.authorMulgaonkar, S.en
dc.contributor.authorTedesco, H.en
dc.contributor.authorOppenheimer, F.en
dc.contributor.authorWalker, R.en
dc.contributor.authorKunzendorf, U.en
dc.contributor.authorRuss, G.en
dc.contributor.authorKnoflach, A.en
dc.contributor.authorPatel, Y.en
dc.contributor.authorFerguson, R.en
dc.date.issued2006en
dc.identifier.citationAmerican Journal of Transplantation Online, 2006; 6(8):1848-1857en
dc.identifier.issn1600-6143en
dc.identifier.issn1600-6143en
dc.identifier.urihttp://hdl.handle.net/2440/35704-
dc.description.abstractFTY720 is a novel immunomodulator being investigated for rejection prophylaxis in renal transplantation when combined with full-dose cyclosporine (CsA; FDC). This 1-year phase II study compared FTY720 plus FDC (Neoral) with FTY720 plus reduced-dose CsA (RDC) and mycophenolate mofetil (MMF) plus FDC in de novo renal transplant patients. Patients were randomized 2:2:2:1 to FTY720 5 mg plus RDC (n = 72); FTY720 2.5 mg plus RDC (n = 74); FTY720 2.5 mg plus FDC (n = 76); or MMF plus FDC (n = 39) for 12 months. CsA exposure in the RDC group was reduced on average by 50% as assessed by C(2) monitoring. The primary efficacy endpoint was the composite incidence of biopsy-proven acute rejection (BPAR), graft loss, death or premature study discontinuation. The incidences for this composite endpoint were 24% and 22%, respectively, for FTY720 5 mg plus RDC and FTY720 2.5 mg plus FDC versus 39% for MMF plus FDC. Patients receiving FTY720 2.5 mg plus RDC were discontinued from treatment due to risk of under-immunosuppression. FTY720 2.5 mg plus FDC and FTY720 5 mg plus RDC were safe and effective in de novo renal transplant patients over 12 months.en
dc.language.isoenen
dc.publisherBlackwell Munksgaarden
dc.subjectFTYA121 study group; Lung; Kidney; Humans; Sphingosine; Propylene Glycols; Cyclosporine; Immunosuppressive Agents; Biopsy; Drug Therapy, Combination; Kidney Transplantation; Graft Rejection; Dose-Response Relationship, Drug; Time Factors; Adult; Middle Aged; Female; Male; Drug-Related Side Effects and Adverse Reactions; Fingolimod Hydrochlorideen
dc.titleFTY720/cyclosporine regimens in de novo renal transplantation: a 1-year dose-finding studyen
dc.typeJournal articleen
dc.identifier.rmid0020062352en
dc.identifier.doi10.1111/j.1600-6143.2006.01404.xen
dc.identifier.pubid51674-
pubs.library.collectionMedicine publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
Appears in Collections:Medicine publications

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