Preclinical safety evaluation of recombinant human interleukin-10

Regul Toxicol Pharmacol. 2002 Feb;35(1):56-71. doi: 10.1006/rtph.2001.1504.

Abstract

Escherichia coli-derived recombinant human interleukin-10 (rhuIL-10) has been evaluated in an extensive series of in vivo and in vitro nonclinical safety studies, including genetic toxicology, single- and repeat-dose systemic toxicity and toxicokinetics, reproductive toxicity, and specialized irritation studies. The primary test species in the toxicology studies were the mouse and monkey based on rhuIL-10 activity in receptor binding and ex vivo cytokine assays. Supported by a detailed preclinical program of therapeutic and prophylactic animal models in autoimmune diseases, the initial clinical development program has focused on investigating the therapeutic potential of rhuIL-10 (Tenovil) in Crohn's disease and rheumatoid arthritis. The results of the subcutaneous toxicity studies, up to 3 months dosing duration in mice and 6 months dosing duration in monkeys, support the development of rhuIL-10 for present and future clinical indications by the subcutaneous route of administration.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Carcinogenicity Tests / methods
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical
  • Haplorhini
  • Humans
  • Injections, Intravenous
  • Injections, Subcutaneous
  • Interleukin-10 / pharmacokinetics
  • Interleukin-10 / standards
  • Interleukin-10 / toxicity*
  • Mice
  • Recombinant Proteins / pharmacokinetics
  • Recombinant Proteins / standards
  • Recombinant Proteins / toxicity*
  • Safety
  • Toxicity Tests / methods*

Substances

  • Recombinant Proteins
  • Interleukin-10