Cyclosporin increases the exposure to tezosentan, an intravenous dual endothelin receptor antagonist

Eur J Clin Pharmacol. 2002 Jul;58(4):243-5. doi: 10.1007/s00228-002-0459-0. Epub 2002 May 23.

Abstract

Objective: To investigate in 12 healthy subjects the pharmacokinetics and tolerability of tezosentan, an endothelin receptor antagonist, when given concomitantly with cyclosporin.

Methods: Tezosentan was infused at a dose of 6.25 mg/h and 25 mg/h for 6 h either alone or following a single dose of 400 mg cyclosporin. Blood and urine samples were collected for pharmacokinetic determinations. Vital signs, electrocardiogram, adverse events, and clinical laboratory parameters were monitored to assess tolerability.

Results: Concomitant cyclosporin resulted in a fourfold increase in the exposure to tezosentan. Tezosentan alone was well tolerated. In combination with cyclosporin, and at both doses, all subjects reported headache, hot flushes and nausea/vomiting, some of which were of severe intensity.

Conclusion: The poor tolerability of the combination of cyclosporin and tezosentan is not correlated with the plasma concentrations of tezosentan.

Publication types

  • Clinical Trial
  • Comparative Study
  • Controlled Clinical Trial

MeSH terms

  • Area Under Curve
  • Cyclosporine / pharmacology*
  • Dose-Response Relationship, Drug
  • Endothelin Receptor Antagonists*
  • Humans
  • Immunosuppressive Agents / pharmacology*
  • Injections, Intravenous
  • Male
  • Pyridines / adverse effects
  • Pyridines / pharmacokinetics*
  • Tetrazoles / adverse effects
  • Tetrazoles / pharmacokinetics*
  • Vasodilator Agents / adverse effects
  • Vasodilator Agents / pharmacokinetics*

Substances

  • Endothelin Receptor Antagonists
  • Immunosuppressive Agents
  • Pyridines
  • Tetrazoles
  • Vasodilator Agents
  • tezosentan
  • Cyclosporine