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PHARMACOKINETICS

FTY720, a Novel Immunomodulator in de Novo Kidney Transplant Patients: Pharmacokinetics and Exposure-Response Relationship

Andrej Skerjanec, PhD, Helio Tedesco, MD, Hans-H. Neumayer, MD, Edward Cole, MD, Klemens Budde, MD, Chyi-Hung Hsu, PhD and Robert Schmouder, MD

From Novartis Pharmaceuticals Corporation, East Hanover, New Jersey (Dr Skerjanec, Dr Hsu, Dr Schmouder); Hospital do Rim e Hipertensão, São Paulo, Brazil (Dr Tedesco); Schwerpunkt Nephrologie, Universitatsklinikum Charite, Berlin, Germany (Dr Neumayer, Dr Budde); and Toronto Hospital, Gen. Division, Toronto, Ontario (Dr Cole).

The pharmacokinetics, safety, and preliminary efficacy of FTY720, a novel immunomodulator, were examined in de novo renal transplant patients. Both noncompartmental and population methods were used to estimate pharmacokinetic estimates in the patients. The steady-state plasma concentrations of FTY720 increased in accordance with maintenance dose level, indicating linearity in clearance and volume of distribution over the 0.25- to 2.5-mg dose range. The pharmacokinetics of FTY720 in de novo renal transplant patients were characterized by the long terminal phase half-life of approximately 200 hours across doses, high volume of distribution (>3000 L), and low clearance (10.8 L/h). The intersubject variation of clearance was 55%, and the intrasubject variation of FTY720 concentrations was 28%. The population analysis revealed significant positive relationships between baseline alkaline phosphatase and clearance, as well as between baseline body weight on apparent volume of distribution. There was no relationship between FTY720 concentrations within a given FTY720 dose cohort and the rate of allograft rejection.


Key Words: Concentration-efficacy relationshipkidney transplantationpopulation methods

Address for reprints: Andrej Skerjanec, PhD, Novartis Pharmaceuticals Corporation, One Health Plaza, East Hanover, NJ 07936; e-mail: andrej.skerjanec{at}novartis.com.


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