- The European Commission (EC) has approved Merck & Co Inc's MRK soluble guanylate cyclase (sGC) stimulator Verquvo (vericiguat).
- Verquvo (2.5 mg, 5 mg, and 10 mg) is indicated to treat symptomatic chronic heart failure in adult patients with reduced ejection fraction who are stabilized after a recent decompensation event requiring intravenous (IV) therapy.
- Merck has the commercial rights to Verquvo in the U.S., and Bayer AG BAYRY has the exclusive commercial rights in the rest of the world.
- In January, the FDA approved Verquvo.
- Price Action: MRK shares are up 0.42% at $76.49 during the premarket session on the last check Wednesday.
- Related content: Benzinga's Full FDA Calendar.
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