Vericiguat: clinical trials recruiting now
FDA drug label
- FDA-approved
- Yes. Vericiguat appears in the FDA drug-label database. Marketed as VERQUVO.
- Drug class
- Soluble Guanylate Cyclase Stimulator (FDA established pharmacologic class)
- Mechanism of action
- Guanylate Cyclase Stimulators (as stated on the FDA label)
- Boxed warning
- The FDA label for Vericiguat carries a boxed warning (the FDA's most serious warning). See the full label for details.
FDA-approved use
VERQUVO ® is indicated to reduce the risk of cardiovascular death and heart failure (HF) hospitalization following a hospitalization for heart failure or need for outpatient IV diuretics, in adults with symptomatic chronic HF and ejection fraction less than 45% [see Clinical Studies (14) ] . VERQUVO is a soluble guanylate cyclase (sGC) stimulator, indicated to reduce the risk of cardiovascular death and heart failure (HF) hospitalization following a hospitalization for heart failure or need for outpatient IV diuretics, in adults with symptomatic chronic HF and ejection fraction less than 45%. ( 1 )
Phase breakdown
Conditions being studied
Recruiting trials involving Vericiguat
- A Study of Real-world Events of Vericiguat in Patients With Chronic Kidney Disease and Heart Failure
- COgnitioN With VERiciGuat Evaluation in Heart Failure
- Vericiguat and Reverse Remodeling Indices in Heart Failure
Common questions
Is Vericiguat FDA-approved?
Yes, marketed as VERQUVO. Its FDA label carries a boxed warning.
How many recruiting trials involve Vericiguat?
3 recruiting trials across 6 conditions.
Is this list of trials complete?
No. For the full record, search ClinicalTrials.gov.