Literature DB >> 18370501

A new oral formulation of tiapride (drops): pharmacokinetic profile and therapeutic applications.

M Canal1, C R Desanti, J P Santoni.   

Abstract

Tiapride is a substituted benzamide widely used in the management of agitation and aggressiveness in the elderly. The development of an oral solution is of particular interest in geriatric medicine and in patients with difficulties swallowing solid formulations. The bioequivalence between a sweetened, flavoured oral drop and tablet forms of tiapride was investigated in a crossover design in 18 healthy male volunteers after a 100mg single-dose administration of each formulation. Plasma concentration profiles were determined. No significant differences in the extent and rate of absorption (t(max), C(max), AUC(0-t) or AUC(0-infinity), C(max )/AUC(0-infinity)) were observed, where t(max) is the time to reach the maximum plasma concentration (C(max)), AUC(0-t) is the area under the concentration-time curve from zero to the last sample at which plasma concentration could be quantified, and AUC(0-infinity) is the area under the curve extrapolated to infinity. The plasma elimination half-lives were similar (4.37 hours and 4.61 hours) and the relative bioavailability of the drop formulation was 99.7%. These results demonstrated the bioequivalence of the two formulations. The drop formulation in this bioequivalence study was the one used for clinical evaluation in the target population of elderly patients experiencing restlessness and aggressive behaviour that was assessed in a prospective double-blind, randomised, previously published trial in 176 patients. In that study, tiapride as a drop formulation compared with melperone was safe and effective with regard to restlessness and aggressive behaviour in elderly patients.

Entities:  

Year:  1998        PMID: 18370501     DOI: 10.2165/00044011-199815050-00010

Source DB:  PubMed          Journal:  Clin Drug Investig        ISSN: 1173-2563            Impact factor:   2.859


  7 in total

1.  Single oral dose pharmacokinetics of tiapride in patients with Huntington's disease.

Authors:  T Norman; E Chiu; R H James; M S Gregory
Journal:  Eur J Clin Pharmacol       Date:  1987       Impact factor: 2.953

2.  Pharmacokinetics of tiapride in patients with tardive dyskinesia and Huntington's disease.

Authors:  R A Roos; E J de Haas; O J Buruma; F A de Wolff
Journal:  Eur J Clin Pharmacol       Date:  1986       Impact factor: 2.953

3.  Functional ability of patients to manage medication packaging: a survey of geriatric inpatients.

Authors:  P A Atkin; T P Finnegan; S J Ogle; G M Shenfield
Journal:  Age Ageing       Date:  1994-03       Impact factor: 10.668

4.  Pharmacokinetics of tiapride and absolute bioavailability of three extravascular forms.

Authors:  E Rey; P d'Athis; M O Richard; D de Lauture; G Olive
Journal:  Int J Clin Pharmacol Ther Toxicol       Date:  1982-02

5.  Measuring the efficacy of psychopharmacological treatment of psychomotoric restlessness in dementia: clinical evaluation of tiapride.

Authors:  H Gutzmann; K P Kühl; S Kanowski; J Khan-Boluki
Journal:  Pharmacopsychiatry       Date:  1997-01       Impact factor: 5.788

Review 6.  Tiapride. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in geriatric agitation.

Authors:  J W Steele; D Faulds; E M Sorkin
Journal:  Drugs Aging       Date:  1993 Sep-Oct       Impact factor: 3.923

Review 7.  Tiapride. A review of its pharmacology and therapeutic potential in the management of alcohol dependence syndrome.

Authors:  D H Peters; D Faulds
Journal:  Drugs       Date:  1994-06       Impact factor: 9.546

  7 in total
  1 in total

1.  Classification of drugs based on properties of sodium channel inhibition: a comparative automated patch-clamp study.

Authors:  Nora Lenkey; Robert Karoly; Peter Lukacs; E Sylvester Vizi; Morten Sunesen; Laszlo Fodor; Arpad Mike
Journal:  PLoS One       Date:  2010-12-20       Impact factor: 3.240

  1 in total

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