Safety, tolerability, and pharmacokinetics of ICL670, a new orally active iron-chelating agent in patients with transfusion-dependent iron overload due to beta-thalassemia

J Clin Pharmacol. 2003 Jun;43(6):565-72.

Abstract

ICL670 is an orally active representative of a new class of tridentate iron chelator developed for the treatment of blood transfusion-dependent iron overload in chronic anemias. In this randomized, double-blind study, patients with transfusion-dependent beta-thalassemia received single oral doses of ICL670 ranging from 2.5 to 80 mg/kg to investigate its safety, tolerability, and pharmacokinetics and to obtain preliminary information on pharmacodynamic effects. ICL670 was well tolerated, and no safety problems occurred up to 80 mg/kg. A plasma half-life of 11 to 19 hours was found for ICL670, supporting once-daily oral administration. AUC0-24 h and Cmax of ICL670 increased nearly proportionally with the dose. The urinary excretion of ICL670 and its iron complex was less than 0.1% of the dose, and this was in accordance with the expected predominant iron fecal excretion induced by ICL670 (based on preclinical experiments). Notwithstanding, a positive trend toward increased amounts of urinary excreted iron was observed when the AUC0-24 h of ICL670 and the iron complex exceeded specific threshold values at the 40- and 80-mg/kg dose levels.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Adult
  • Area Under Curve
  • Benzoates* / adverse effects
  • Benzoates* / pharmacokinetics
  • Benzoates* / therapeutic use
  • Deferasirox
  • Double-Blind Method
  • Half-Life
  • Humans
  • Iron / urine
  • Iron Chelating Agents* / pharmacokinetics
  • Iron Chelating Agents* / therapeutic use
  • Male
  • Safety
  • Triazoles* / adverse effects
  • Triazoles* / pharmacokinetics
  • Triazoles* / therapeutic use
  • beta-Thalassemia* / drug therapy
  • beta-Thalassemia* / metabolism

Substances

  • Benzoates
  • Iron Chelating Agents
  • Triazoles
  • Iron
  • Deferasirox