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Sitaxsentan, a selective endothelin-A receptor antagonist for the treatment of pulmonary arterial hypertension.

Abstract
Sitaxsentan, a highly selective endothelin-A (ET(A)) receptor antagonist (6500-fold more selective for ET(A) receptors than endothelin-B (ET(B)) receptors), may benefit patients with pulmonary artery hypertension (PAH) by blocking the vasoconstrictor effects of ET(A) receptors while maintaining the vasodilator/clearance functions of ET(B) receptors. In its first randomised, placebo-controlled study, Sitaxsentan to Relieve Impaired Exercise-1 (STRIDE-1), sitaxsentan improved exercise capacity assessed by 6 min walk, 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 PAH, PAH related to connective tissue disease or PAH related to congenital heart disease. In STRIDE-1, doses of 100 and 300 mg/day p.o. were evaluated. Although both doses showed equivalent efficacy, the lower dose had a more tolerable safety profile. Additional studies are ongoing to assess the relative safety and efficacy of 50 and 100 mg/day doses, both in de novo patients and in patients previously treated with the ET(A)/ET(B) receptor antagonist bosentan. Long-term comparative studies are necessary to determine whether there is a clinically meaningful difference between selective ET(A) receptor antagonism and ET(A)/ET(B) receptor antagonism.
AuthorsEvelyn M Horn, Allison C Widlitz, Robyn J Barst
JournalExpert opinion on investigational drugs (Expert Opin Investig Drugs) Vol. 13 Issue 11 Pg. 1483-92 (Nov 2004) ISSN: 1744-7658 [Electronic] England
PMID15500395 (Publication Type: Journal Article)
Chemical References
  • Endothelin A Receptor Antagonists
  • Endothelin B Receptor Antagonists
  • Isoxazoles
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Thiophenes
  • sitaxsentan
Topics
  • Adult
  • Endothelin A Receptor Antagonists
  • Endothelin B Receptor Antagonists
  • Humans
  • Hypertension, Pulmonary (drug therapy)
  • Isoxazoles (administration & dosage, adverse effects, chemistry, therapeutic use)
  • Male
  • Middle Aged
  • Receptor, Endothelin A (metabolism)
  • Receptor, Endothelin B (metabolism)
  • Substrate Specificity
  • Thiophenes (administration & dosage, adverse effects, chemistry, therapeutic use)

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