Arteether administration in humans: preliminary studies of pharmacokinetics, safety and tolerance

Trans R Soc Trop Med Hyg. 1994 Jun:88 Suppl 1:S53-4. doi: 10.1016/0035-9203(94)90475-8.

Abstract

The recently developed artemisinin derivative arteether was administered by intramuscular injection to healthy male subjects in a single dose (n = 23) and a multiple dose study (n = 27). The drug was well tolerated. Clinical, neurological, electrocardiographic and biochemical monitoring did not reveal significant toxicity. Apart from some increase in eosinophil numbers, no haematological abnormality was seen. Preliminary pharmacokinetic data showed a long elimination half life of 25-72 h and marked accumulation in the multiple dose study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antimalarials / administration & dosage
  • Antimalarials / pharmacokinetics*
  • Antimalarials / pharmacology
  • Antiprotozoal Agents / administration & dosage
  • Antiprotozoal Agents / pharmacokinetics*
  • Antiprotozoal Agents / pharmacology
  • Artemisinins*
  • Drug Tolerance
  • Humans
  • Injections, Intramuscular
  • Male
  • Sesquiterpenes / administration & dosage
  • Sesquiterpenes / pharmacokinetics*
  • Sesquiterpenes / pharmacology

Substances

  • Antimalarials
  • Antiprotozoal Agents
  • Artemisinins
  • Sesquiterpenes
  • artemotil