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Sitaxsentan: a novel endothelin-A receptor antagonist for pulmonary arterial hypertension.

Abstract
Sitaxsentan is an orally active, selective endothelin-A receptor antagonist that may benefit patients with pulmonary arterial hypertension by blocking the vasoconstrictive effects of endothelin-A receptors, while maintaining the vasodilator and endothelin-1 clearance functions of the endothelin-B receptors. In its first randomized, placebo-controlled study, sitaxsentan improved exercise capacity assessed by the 6-min walk test, New York Heart Association functional class, cardiac index and pulmonary vascular resistance in New York Heart Association Class II, III and IV patients with idiopathic pulmonary arterial hypertension and pulmonary arterial hypertension related to connective tissue disease or congenital heart disease. Although doses of 100 and 300 mg once daily demonstrated equivalent efficacy, the lower dose had a better safety profile. Additional studies are ongoing to assess the relative safety and efficacy of 50 and 100 mg once-daily dosing. The most common side effects include rhinitis, headache, peripheral edema, chest pain, nausea, constipation, increased prothrombin time/international normalized ratio (in patients on warfarin), flushing and insomnia. As with other endothelin receptor antagonists, increases in hepatic transaminases have been observed with sitaxsentan. Initial studies using the selective oral endothelin-A receptor antagonist sitaxsentan in pulmonary arterial hypertension patients have revealed a favorable risk-benefit therapeutic profile with the 100 mg once-daily dose.
AuthorsAllison C Widlitz, Robyn J Barst, Evelyn M Horn
JournalExpert review of cardiovascular therapy (Expert Rev Cardiovasc Ther) Vol. 3 Issue 6 Pg. 985-91 (Nov 2005) ISSN: 1744-8344 [Electronic] England
PMID16292989 (Publication Type: Journal Article, Review)
Chemical References
  • Endothelin Receptor Antagonists
  • Isoxazoles
  • Thiophenes
  • sitaxsentan
Topics
  • Clinical Trials as Topic
  • Endothelin Receptor Antagonists
  • Humans
  • Hypertension, Pulmonary (drug therapy)
  • Isoxazoles (adverse effects, therapeutic use)
  • Thiophenes (adverse effects, therapeutic use)

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