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Bayer/Merxton guanylate cyclase agonist approved in the EU for the treatment of heart failure

 Last Update: 2021-08-15
 Source: Internet
 Author: User

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Article Source: Immediate Medicine News

On July 21st, Merck (MSD) and Bayer (Bayer) jointly announced that the European Commission (EC) has approved the listing of its soluble guanylate cyclase (sGC) stimulant Verquvo (vericiguat) for the treatment of adults with reduced ejection fraction Patients with symptomatic chronic heart failure who have stabilized after a recent decompensated event that required intravenous (IV) therapy

Reduced ejection fraction (HFrEF) heart failure, formerly known as systolic heart failure, is characterized by impaired ability of the heart to eject blood adequately during its contraction phase

Heart failure is related to nitric oxide (NO) synthesis disorder and decreased sGC activity

Verquvo was jointly developed by Merck and Bayer.

Note: The original text has been deleted

Reference materials:

[1] VERQUVO® (vericiguat) Approved in the European Union.

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