Phase I and pharmacokinetic study of 502U83 (an arylmethylaminopropanediol) in cancer patients

Anticancer Drugs. 1992 Jun;3(3):219-24. doi: 10.1097/00001813-199206000-00003.

Abstract

502U83, a novel arylmethylaminopropanediol, has proven active in vivo against a panel of murine leukemia and solid tumors as well as in a tumor clonogenic assay against a variety of fresh human cancers. A total of 35 previously treated cancer patients were enrolled in a phase I study of this compound. The maximally tolerated dose (MTD) appears to be 12,800 mg/m2/72 h by continuous intravenous infusion with severe granulocytopenia occurring in three of five patients. There were no objective clinical responses. Serum pharmacokinetic parameters were as follows: plasma terminal phase half-life (t1/2 beta) = 3.84 h; total body clearance (CLB) = 53.1 l/h/m2; volume of distribution at steady state (Vdss) = 127.9 l/m2; maximum plasma concentration (Cmax) = 3.7 micrograms/ml (at 12,800 mg/m2/72 h dose).

MeSH terms

  • Anthracenes / adverse effects
  • Anthracenes / pharmacokinetics
  • Anthracenes / therapeutic use*
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / therapeutic use*
  • Chromatography, High Pressure Liquid
  • Drug Evaluation
  • Female
  • Half-Life
  • Humans
  • Intercalating Agents / adverse effects
  • Intercalating Agents / pharmacokinetics
  • Intercalating Agents / therapeutic use*
  • Male
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism

Substances

  • Anthracenes
  • Antineoplastic Agents
  • Intercalating Agents
  • 502U83