The effects of sitaxentan on sildenafil pharmacokinetics and pharmacodynamics in healthy subjects

Br J Clin Pharmacol. 2010 Jan;69(1):23-6. doi: 10.1111/j.1365-2125.2009.03541.x.

Abstract

What is already known about this subject: * Endothelin-A receptor antagonists (ETRAs) and phosphodiesterase-type 5 inhibitors are approved monotherapies for the treatment of pulmonary arterial hypertension; combining agents from these two drug classes could be beneficial. * There is a significant pharmacokinetic (PK) interaction between the ETRA bosentan and the phosphodiesterase-type 5 inhibitor sildenafil. * This study assessed whether the ETRA sitaxentan similarly impacts the PK of sildenafil.

What this study adds: * This study demonstrates that sitaxentan has little effect on sildenafil PK and pharmacodynamics and that no dose adjustment of either agent is required upon co-administration of sildenafil with sitaxentan.

Aims: This study evaluated the effects of sitaxentan on the pharmacodynamic [systemic blood pressure (BP)] and pharmacokinetic (PK) parameters of sildenafil in healthy volunteers.

Methods: Healthy subjects (18-60 years, n= 24) were randomized into two sequence groups. Group 1 received sitaxentan sodium 100 mg daily (7 days), followed by placebo (7 days). Group 2 received placebo (7 days), followed by sitaxentan sodium 100 mg (7 days). On day 7 of each treatment period, participants received sildenafil 100 mg. PK parameters and BP were analysed on day 7 in each treatment period.

Results: Sildenafil exposure was slightly higher [AUC(infinity) geometric mean ratio (GMR), 128%] when co-administered with sitaxentan 100 mg vs. placebo, demonstrating a weak, but statistically significant interaction (90% confidence interval 115.5%, 141.2%). The mean maximum positive (E(max)+) and maximum negative (E(max)-) changes from baseline in both systolic and diastolic BP were comparable for sitaxentan and placebo (range 4.8-7.3 mmHg) with three of four geometric mean ratios falling within the equivalence window, suggesting that the drug interaction was not clinically significant. Adverse events were similar between sitaxentan 100 mg (39%) and placebo (30%). No deaths or serious adverse events occurred during the study.

Conclusion: The dose of sildenafil does not need to be adjusted when co-administered with sitaxentan.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Area Under Curve
  • Blood Pressure / drug effects
  • Drug Interactions
  • Drug Therapy, Combination
  • Endothelin Receptor Antagonists*
  • Female
  • Humans
  • Isoxazoles / pharmacology*
  • Male
  • Middle Aged
  • Piperazines / pharmacokinetics*
  • Piperazines / pharmacology
  • Purines / pharmacokinetics
  • Purines / pharmacology
  • Sildenafil Citrate
  • Sulfones / pharmacokinetics*
  • Sulfones / pharmacology
  • Thiophenes / pharmacology*
  • Vasodilator Agents / pharmacokinetics*
  • Vasodilator Agents / pharmacology
  • Young Adult

Substances

  • Endothelin Receptor Antagonists
  • Isoxazoles
  • Piperazines
  • Purines
  • Sulfones
  • Thiophenes
  • Vasodilator Agents
  • Sildenafil Citrate
  • sitaxsentan