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

Eur J Clin Pharmacol. 1987;32(6):583-6. doi: 10.1007/BF02455992.

Abstract

The pharmacokinetic properties of a single oral dose of 100 mg of tiapride were studied in six patients with Huntington's disease. The results for five patients were consistent with a two compartment open model. Peak plasma concentrations were observed within 2 h following drug administration with a mean value of 0.92 micrograms/ml being recorded. The drug was rapidly eliminated as unmetabolised tiapride in the urine, 51% of the dose was recovered in 24 h. The plasma elimination half-life was 5.3 h and the average apparent plasma clearance was 16.6 l/h.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Benzamides / pharmacokinetics*
  • Female
  • Half-Life
  • Humans
  • Huntington Disease / metabolism*
  • Kidney / metabolism
  • Male
  • Middle Aged
  • Tiapamil Hydrochloride / pharmacokinetics*

Substances

  • Benzamides
  • Tiapamil Hydrochloride