The following drug information is obtained from various newswires, published
medical journal articles, and medical conference presentations.
reduction of thrombotic cardiovascular events
Zontivity (vorapaxar) is a protease-activated receptor-1 (PAR-1) antagonist.
Zontivity is specifically indicated for the reduction of thrombotic cardiovascular events in patients with a history of myocardial infarction (MI) or with peripheral
arterial disease (PAD).
Zontivity is supplied as a tablet for oral administration. The recommended dose is one tablet (2.08 mg) orally once daily, with or without food.
The FDA approval of Zontivity was based on TRA 2°P - TIMI 50. TRA 2°P was a multicenter, randomized, double-blind, placebo-controlled study conducted in patients who had evidence or a history of atherosclerosis involving the coronary, cerebral (ischemic stroke), or peripheral vascular
systems. Subjects were randomized to receive daily treatment with Zontivity (n=13,225) or placebo (n=13,224) in addition to standard of care. The study’s primary endpoint was the composite of cardiovascular death, MI, stroke, and urgent coronary revascularization (UCR). The composite of cardiovascular death, MI, and stroke was assessed as key secondary endpoint. The median follow-up was 2.5 years (up to 4 years). The findings in all randomized patients for the primary efficacy composite endpoint show a 3-year
K-M event rate of 11.2% in the Zontivity group compared to 12.4% in the placebo group (p=0.001). The findings for the key secondary efficacy endpoint show a 3-year Kaplan-Meier (K-M) event rate of 9.3% in the Zontivity group compared to 10.5% in placebo group (p<0.001).
Adverse effects associated with the use of Zontivity may include, but are not limited to, the following:
- bleeding, including life-threatening and fatal bleeding
Mechanism of Action
Zontivity (varapaxar) s a reversible antagonist of the protease-activated receptor-1 (PAR-1) expressed on platelets, but its long half-life makes it effectively irreversible. Vorapaxar inhibits thrombin-induced and thrombin receptor agonist peptide (TRAP)-induced platelet aggregation in in vitro studies. Vorapaxar does not inhibit platelet aggregation induced by adenosine diphosphate (ADP), collagen or a thromboxane mimetic and does not affect coagulation parameters ex vivo. PAR-1 receptors are also expressed in a wide variety of cell types, including endothelial cells, neurons, and smooth muscle cells, but the pharmacodynamic effects of vorapaxar in these cell types have not been assessed.
For additional information regarding Zontivity or the reduction of thrombotic cardiovascular events in patients with a history of MI or PAD, please visit the Zontivity web page.