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In 2021, the U.S. FDA approved vericiguat for patients with heart failure with reduced ejection fraction (HFrEF) after VICTORIA researchers found that the soluble guanylate cyclase stimulator lowered the risk for cardiovascular death or HF hospitalization in patients with a recent decompensation (i.e., HF hospitalization within 6 months or receipt of outpatient intravenous diuretics within 3 months). Investigators further explore this therapy’s effectiveness in two manufacturer-sponsored studies.
VICTOR was a placebo-controlled trial of vericiguat in ≈6000 ambulatory patients with HFrEF but without a recent HF event. Rates of guideline-based drug and device therapy were high. Vericiguat did not reduce time to cardiovascular…