Ambrisentan (ambrisentan)

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Ambrisentan, a selective propionic-acid endothelin-1 (ET-1) type A receptor antagonist, is a vasodilator.

Ambrisentan, a selective endothelin-1 (ET-1) type A receptor antagonist, is a vasodilator. Increased concentrations of ET-1, a potent vasoconstrictor, have been detected in the plasma and lung tissue of patients with pulmonary arterial hypertension (PAH), suggesting a pathogenic role for ET-1 in this disorder. Two ET-1 receptor subtypes, type A and type B, have been identified; activation of ET-1 type A receptors primarily mediates vasoconstriction and smooth muscle cell proliferation, while activation of ET-1 type B receptors results in vasodilation and facilitates clearance of ET-1.

Ambrisentan is approximately 4000-fold more selective for the type A receptor compared with the type B receptor; however, the clinical implications of this selectivity remain to be established.

Ambrisentan exhibits dose proportional pharmacokinetics in healthy adults. The absolute bioavailability is unknown, and peak concentrations occur approximately 2 hours after oral administration in healthy subjects and PAH patients. Food does not affect bioavailability of the drug.

Ambrisentan is highly protein bound (99%). The drug is predominantly eliminated by non-renal pathways. The terminal half-life is 15 hours, but the effective half-life is about 9 hours.

In vitro evidence indicates that ambrisentan is metabolized by cytochrome P-450 (CYP) isoenzymes 3A4 and 2C19, and by uridine diphosphate-glucuronosyltransferases (UGT) 1A9, 2B7, and 1A3. In vitro studies suggest that ambrisentan also is a substrate of the transporters p-glycoprotein and organic anion transport protein (OATP).

USES: Ambrisentan is used to treat high blood pressure in the lungs (pulmonary arterial hypertension). This condition is thought to be caused by increased levels of a certain natural substance (endothelin-1). This medication blocks the effects of endothelin-1, thereby helping to decrease the blood pressure in the lungs, slow the worsening of symptoms, and improve your ability to exercise.

Generic name: ambrisentan
Pronunciation: (AM-bri-SEN-tan)

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Ambrisentan:

  • Pulmonary Arterial Hypertension

Also known as: Hypertensive Pulmonary Arterial Disease, Pulmonary Hypertensive Arterial Disease.

Dosing

No dosing information is available for this tab.

Drug interactions

In vitro studies indicate that ambrisentan is metabolized by cytochrome P-450 (CYP) isoenzymes 3A4 and 2C19 and by uridine 5'-diphosphate glucuronosyltransferases (UGTs; uridine diphosphoglucuronosyltransferase, UDP-glucuronate beta-d-glucuronosyltransferase (acceptor-unspecific)) 1A9S, 2B7S, and 1A3S. The drug appears to be a substrate, but not an inhibitor, of the organic anion transport protein (OATP) and the P-glycoprotein (P-gp) transport system. At clinically relevant concentrations, ambrisentan does not inhibit or induce CYP enzymes.

Contraindications

*Pregnancy.

*Idiopathic pulmonary fibrosis, with or without pulmonary hypertension (WHO group 3).

Adverse reactions

The most common adverse effects (>3%) of ambrisentan in clinical studies were peripheral edema, nasal congestion, sinusitis, and flushing.

When used in combination with tadalafil, the most common adverse effects (>5% compared to either monotherapy) were peripheral edema, headache, nasal congestion, cough, anemia, dyspepsia, and bronchitis.

Precautions

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ICD codes

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Formulary status

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Last reviewed · Source: First Databank (FDB) drug data