The effects of sitaxentan on sildenafil pharmacokinetics and pharmacodynamics in healthy subjects
Author(s)
Stavros, F
Kramer, WG
Wilkins, MR
Type
Journal Article
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.
Date Issued
2010-01
Date Acceptance
2009-09-01
Citation
British Journal of Clinical Pharmacology, 2010, 69 (1), pp.23-26
ISSN
0306-5251
Publisher
British Pharmacological Society
Start Page
23
End Page
26
Journal / Book Title
British Journal of Clinical Pharmacology
Volume
69
Issue
1
Copyright Statement
© 2010 The Authors. Journal compilation © 2010 The British Pharmacological Society. Re‐use of this article is permitted in accordance with the Terms and Conditions set out at https://authorservices.wiley.com/author-resources/Journal-Authors/licensing/onlineopen-without-a-creative-commons-license.html
Identifier
https://bpspubs.onlinelibrary.wiley.com/doi/full/10.1111/j.1365-2125.2009.03541.x
Subjects
Science & Technology
Life Sciences & Biomedicine
Pharmacology & Pharmacy
blood pressure
N-desmethylsildenafil
pharmacokinetics
sildenafil
sitaxentan
HYPERTENSION
BOSENTAN
Adult
Area Under Curve
Blood Pressure
Drug Interactions
Drug Therapy, Combination
Endothelin Receptor Antagonists
Female
Humans
Isoxazoles
Male
Middle Aged
Piperazines
Purines
Sildenafil Citrate
Sulfones
Thiophenes
Vasodilator Agents
Young Adult
Humans
Sulfones
Isoxazoles
Piperazines
Thiophenes
Purines
Vasodilator Agents
Drug Therapy, Combination
Area Under Curve
Blood Pressure
Drug Interactions
Adult
Middle Aged
Female
Male
Young Adult
Endothelin Receptor Antagonists
Sildenafil Citrate
1115 Pharmacology and Pharmaceutical Sciences
Pharmacology & Pharmacy
Publication Status
Published
Date Publish Online
2009-09-22