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Published Online, 28 October 2008, www.theannals.com, DOI 10.1345/aph.1L014.
The Annals of Pharmacotherapy: Vol. 42, No. 11, pp. 1653-1659. DOI 10.1345/aph.1L014
© 2008 Harvey Whitney Books Company.
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NEW DRUG APPROVALS

Role of Ambrisentan in the Management of Pulmonary Hypertension

Sandra L Hrometz, PhD

Associate Professor of Pharmacology, Department of Pharmaceutical and Biomedical Sciences, Raabe College of Pharmacy, Ohio Northern University, Ada, OH

Kelly M Shields, PharmD

Assistant Professor of Pharmacy Practice, Department of Pharmacy Practice, Raabe College of Pharmacy, Ohio Northern University

Reprints: Dr. Hrometz, Department of Pharmaceutical and Biomedical Sciences, Raabe College of Pharmacy, Ohio Northern University, Ada, OH 45810, fax 419/772-1917, s-hrometz{at}onu.edu

OBJECTIVE: To review the role of ambrisentan in the treatment of pulmonary arterial hypertension (PAH).

DATA SOURCES: Literature was accessed through MEDLINE (1950–June 2008), Iowa Drug Information Service (1966–March 2008), EMBASE (1966–June 2008), bibliographies of pertinent articles, and unpublished data provided by the manufacturer and the Food and Drug Administration (FDA). Search terms included ambrisentan, endothelin antagonist, pulmonary hypertension, and pulmonary arterial hypertension. Due to limited literature available, additional criteria to limit searches were not used.

STUDY SELECTION AND DATA EXTRACTION: Abstracts and original preclinical and clinical research reports available in the English language were identified for review. All manufacturer-provided data were also evaluated. Literature related to ambrisentan, endothelin antagonists, pulmonary hypertension, and pulmonary arterial hypertension were included. Four clinical trials evaluated the efficacy of ambrisentan in adults with symptomatic PAH.

DATA SYNTHESIS: Ambrisentan is the latest endothelin-receptor antagonist (ERA) to obtain FDA approval for the treatment of PAH. It joins the first FDA-approved ERA, bosentan. Like bosentan, ambrisentan is available orally (with once-daily dosing compared with bosentan's twice-daily dosing) and has been shown to improve exercise capacity and delay clinical worsening. As with bosentan, the most significant safety concerns with ambrisentan relate to potential liver injury and a contraindication in pregnancy. Although ambrisentan has higher affinity for the endothelin type A receptor than for the endothelin type B receptor, specific advantages of this selectivity, in terms of efficacy compared with bosentan, a nonselective agent, have not been demonstrated.

CONCLUSIONS: Ambrisentan has been shown to be an effective ERA in patients with PAH. A significant advantage of ambrisentan is the lack of any clinically important drug interactions with warfarin and sildenafil, which are frequently used by patients being treated for PAH.

Key Words: ambrisentan, endothelin antagonist, pulmonary arterial hypertension, pulmonary hypertension

Published Online, October 28, 2008. www.theannals.com, DOI 10.1345/aph.1L014

THIS ARTICLE IS APPROVED FOR CONTINUING EDUCATION CREDIT
ACPE UNIVERSAL PROGRAM NUMBER:
407-000-08-022-H01-P





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