VERQUVO (vericiguat) by Merck & Co. is guanylate cyclase stimulators [moa]. Approved for soluble guanylate cyclase stimulator [epc]. First approved in 2021.
Drug data last refreshed 4h ago · AI intelligence enriched 1w ago
VERQUVO (vericiguat) is an oral soluble guanylate cyclase stimulator approved by FDA in January 2021 for heart failure management. It works by activating the soluble guanylate cyclase pathway to improve cardiac function and reduce hospitalizations. The drug represents a novel mechanism within the heart failure treatment armamentarium.
Product is in peak revenue stage with established market penetration; commercial teams should expect stable headcount and mature field infrastructure.
Guanylate Cyclase Stimulators
Soluble Guanylate Cyclase Stimulator
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
An Observational Study to Learn More About How Safe Vericiguat is and How Well it Works in Indian People With Chronic Heart Failure With Reduced Ejection Fraction and Worsening Chronic Heart Failure Under Real World Conditions
The Impact of Vericiguat on Microvascular Function in Patients with Documented Vasospastic Angina Pectoris
An Observational Study to Learn More About the Real-world Outcomes in Patients With Heart Failure Who Initiate Treatment With Vericiguat in Japan
An Observational Study Called ROVER to Learn More About How Well Vericiguat Works in People Who Were Newly Treated With Vericiguat in Routine Medical Care in Germany
A Study to Learn About the Taste of Vericiguat Given in Liquid Form in Healthy Male Participants Aged 18 to 45 Years
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moWorking on VERQUVO offers exposure to a peak-stage, established cardiovascular asset with stable revenue but declining growth horizon. Positions emphasize commercial execution, payer defense, and patient access over innovation and clinical development; expect mature organizational processes and experienced cross-functional teams.