| Literature DB >> 17589349 |
Sander Florman1, Rita Alloway, Munci Kalayoglu, Jeffrey Punch, Thomas Bak, Joseph Melancon, Goran Klintmalm, Stephan Busque, Michael Charlton, John Lake, Shobha Dhadda, Kathleen Wisemandle, Mary Wirth, William Fitzsimmons, John Holman, M Roy First.
Abstract
Compliance with complex immunosuppressant drug therapies in transplant recipients might be improved with regimens that require less frequent dosing. A once-daily extended release (XL) formulation of tacrolimus has been developed that allows a 1:1 conversion from the twice-a-day tacrolimus (TAC) formulation and has a good exposure to trough concentration correlation. In an open-label, multicenter study, stable liver transplant recipients (n=69) were converted from twice-a-day TAC to XL once-daily in the morning, and were maintained for at least 2 years postconversion using the same therapeutic monitoring and patient care techniques employed with TAC. Two years after conversion, the incidence of biopsy-confirmed acute rejection was 5.8% (4 of 69); patient and graft survival was 98.6% (68 of 69). The safety profile of XL was consistent with that previously reported for TAC. Liver transplant recipients can be converted from twice-a-day TAC to once-daily XL and maintained for at least 2 years postconversion with neither unique efficacy nor safety concerns.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17589349 DOI: 10.1097/01.tp.0000265445.09987.f1
Source DB: PubMed Journal: Transplantation ISSN: 0041-1337 Impact factor: 4.939