APPLICATION OF POPULATION PHARMACOKINETICS TO THE PHASE-II DEVELOPMENT OF AN ANTI-ALZHEIMERS DISEASE COMPOUND, S12024

Citation
C. Laveille et al., APPLICATION OF POPULATION PHARMACOKINETICS TO THE PHASE-II DEVELOPMENT OF AN ANTI-ALZHEIMERS DISEASE COMPOUND, S12024, Journal of clinical pharmacology, 38(4), 1998, pp. 315-323
Citations number
9
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00912700
Volume
38
Issue
4
Year of publication
1998
Pages
315 - 323
Database
ISI
SICI code
0091-2700(1998)38:4<315:AOPPTT>2.0.ZU;2-J
Abstract
Steady-state concentrations of S12024, a novel compound for treatment of Alzheimer's disease, were studied to determine the pharmacokinetic parameters of S12024 in Phase IIa patients and to assess the effect of patient characteristics on those pharmacokinetics. A prospective spar se sampling strategy was used to obtain oral repeated data (n = 285) f rom 89 patients, which were analyzed using a one-compartment model and the NONMEM computer program. The model suggested that apparent cleara nce of S12024 was influenced by the study and by patient age. In the S panish study, apparent clearance was increased by 68% and 26% for dose s of 100 mg and 300 mg, respectively, and patient age decreased oral c learance by approximately 10% per decade in the patient age range (50 to 90 years). Data from only a few patients in the Spanish study were probably responsible for the observed study influence on apparent clea rance of S12024, and no measured covariates could explain this effect. The model provided an excellent characterization of the observed data and it predicted correctly the plasma concentrations from an earlier Phase I trial and a subsequent Phase IIb study. The present model, bui lt from Phase IIa data, provides a basis for examining the influence o f patient covariates and the magnitude of their effects on the pharmac okinetics of S12024. The study effect is probably an artefact that wil l disappear by further expanding of the population model in the future . (C)1998 The American College of Clinical Pharmacology.