The clinical pharmacokinetics of single doses of estazolam

Am J Med. 1990 Mar 2;88(3A):2S-5S. doi: 10.1016/0002-9343(90)90278-l.

Abstract

The pharmacokinetics of estazolam were examined in 17 healthy male subjects. Plasma concentration-time profiles were compared following the oral administration of one 1-mg tablet, two 1-mg tablets, and one 2-mg tablet. No statistically significant differences were detected among the mean time of maximal plasma concentration (Tmax), maximal plasma concentration (Cmax), area under the plasma concentration-time curve from zero to 72 hours (AUC), or half-life values for the 2-mg doses. Mean Cmax was 97.7 and 98.6 ng/ml and mean Tmax was 1.9 and 1.6 hours for two 1-mg tablets and one 2-mg tablet, respectively. Proportionately decreased Cmax and AUC were observed following the 1-mg dose. Mean Cmax was 54.7 ng/ml for the 1-mg dose. Mean Tmax and elimination half-life values were similar to those observed after the 2-mg doses. The overall harmonic mean half-life was 14.4 hours.

MeSH terms

  • Administration, Oral
  • Adolescent
  • Adult
  • Anti-Anxiety Agents / pharmacokinetics*
  • Chromatography, High Pressure Liquid
  • Estazolam / administration & dosage
  • Estazolam / blood
  • Estazolam / pharmacokinetics*
  • Half-Life
  • Humans
  • Male
  • Random Allocation
  • Tablets
  • Time Factors

Substances

  • Anti-Anxiety Agents
  • Tablets
  • Estazolam