Safety evaluation of recombinant human interleukin-4. II. Clinical studies

Clin Immunol Immunopathol. 1997 Apr;83(1):12-4. doi: 10.1006/clin.1997.4304.

Abstract

The safety and tolerability of Escherichia coli-derived recombinant human interleukin-4 (rhuIL-4) have been evaluated in phase I and phase II studies in human patients with a variety of malignancies. Clinical trials have demonstrated that subcutaneous administration of rhuIL-4 is safe and well tolerated at doses as high as 5 micrograms/kg/day and as high as 10 micrograms/kg when administered 3 times/week. Although preclinical safety studies in cynomolgus monkeys demonstrated a number of adverse effects following repeated daily dosing with rhuIL-4, similar effects have generally not been observed in human patients.

MeSH terms

  • Animals
  • Clinical Trials, Phase I as Topic
  • Clinical Trials, Phase II as Topic
  • Dose-Response Relationship, Drug
  • Humans
  • Interleukin-4 / standards*
  • Interleukin-4 / therapeutic use*
  • Interleukin-4 / toxicity
  • Neoplasms / drug therapy
  • Recombinant Proteins / standards
  • Recombinant Proteins / therapeutic use
  • Recombinant Proteins / toxicity

Substances

  • Recombinant Proteins
  • Interleukin-4