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Titolo:
Single- and multiple-dose pharmacokinetics of ziprasidone under non-fasting conditions in healthy male volunteers
Autore:
Miceli, JJ; Wilner, KD; Hansen, RA; Johnson, AC; Apseloff, G; Gerber, N;
Indirizzi:
Pfizer Inc, Cent Res, Dept Clin Res, Groton, CT 06340 USA Pfizer Inc Groton CT USA 06340 t Res, Dept Clin Res, Groton, CT 06340 USA Ohio State Univ, Dept Pharmacol, Columbus, OH 43210 USA Ohio State Univ Columbus OH USA 43210 t Pharmacol, Columbus, OH 43210 USA
Titolo Testata:
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY
, volume: 49, anno: 2000, supplemento:, 1
pagine: 5S - 13S
SICI:
0306-5251(2000)49:<5S:SAMPOZ>2.0.ZU;2-N
Fonte:
ISI
Lingua:
ENG
Soggetto:
RISPERIDONE; MEN; HYPERPROLACTINEMIA; SCHIZOPHRENIA; HALOPERIDOL; CP-88,059; DRUGS;
Keywords:
extrapyramidal symptoms; pharmacokinetics; serum prolactin; ziprasidone;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Life Sciences
Citazioni:
28
Recensione:
Indirizzi per estratti:
Indirizzo: Miceli, JJ Pfizer Inc, Cent Res, Dept Clin Res, Groton, CT 06340 USA Pfizer Inc Groton CT USA 06340 Clin Res, Groton, CT 06340 USA
Citazione:
J.J. Miceli et al., "Single- and multiple-dose pharmacokinetics of ziprasidone under non-fasting conditions in healthy male volunteers", BR J CL PH, 49, 2000, pp. 5S-13S

Abstract

Aims To evaluate the pharmacokinetics and tolerability of single and multiple oral doses of ziprasidone in healthy male volunteers, and to determine the influence of ziprasidone on serum prolactin levels. Methods Single and multiple doses of ziprasidone were given orally (as twodivided daily doses), at fixed dosages of 10 and 40 mg day(-1), and using titrated regimens of 40-80 and 40-120 mg day(-1), for 14 days. All dosages were taken immediately after food. The study adopted a randomized, double-blind, placebo-controlled design. Prolactin response, sedative properties, tolerability, and extrapyramidal symptoms were also investigated. Results Steady-state exposure to ziprasidone was attained after 1 day of dosing. Mean C-max and AUC(0,12h) increased with increasing dose, with apparent dose-proportionality between the 20 and 60 mg dose levels. Trough-to-peak ratios at steady state ranged from 2 to 5. Accumulation ratios fbr the fixed-dose regimens were 1.49 and 1.48 at the 5 and 20 mg dose levels, respectively. Ziprasidone was associated with transient prolactin elevation but levels of prolactin returned to baseline within the dosing interval at steady state. There was a marginal, transient increase in serum prolactin levels which was not dose-related at the 80 and 120 mg day(-1) doses, and which was noted to attenuate with chronic dosing. Ziprasidone was generally well tolerated. The most frequent side-effect was mild or moderate headache. A minority of patients suffered first-dose postural hypotension. Ziprasidone was also associated with a mild sedative effect that became less pronounced as treatment continued. There were no drug-related changes in electrocardiogram or clinical laboratory variables that were of clinical importance. Conclusions Ziprasidone is characterized by a predictable pharmacokinetic profile resulting in symptoms that reflect its pharmacological action.

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Documento generato il 20/01/20 alle ore 23:05:32