Bayer and partner Merck & Co. have carried a new heart failure drug across the FDA finish line, hoping to carve blockbuster share out of an ever-more-competitive field. As industry watchers see it, the two will have a hard time getting there in the face of stepped-up competition from Novartis and AstraZeneca.
The FDA Tuesday approved Verquvo, or vericiguat, to treat patients with chronic heart failure with reduced ejection fraction (HFrEF). The go-ahead is limited to a group of high-risk patients who’ve recently been hospitalized or received diuretics as outpatients for acute decompensated heart failure.
Now, Verquvo’s entering a market where Novartis’ fast-growing Entresto is establishing itself as the new standard of care and the SGLT2 class of diabetes drugs is trying to win a place with AstraZeneca’s recent landmark approval for Farxiga.
Bayer, the original developer of Verquvo, has pegged peak sales at €1 billion. The German company shares the drug’s responsibilities 50-50 with Merck through a deal signed in 2014. But analysts believe the drug has a smaller role to play as physicians will likely save it for last-line treatment in sicker patients.
Based on the approval—and a failed phase 2 Vitality trial in heart failure with preserved ejection fraction (HFpEF)—SVB Leerink analyst Daina Graybosch in a Wednesday note projected a “very slow sales ramp” for Verquvo, with 2021 U.S. sales to be in “low single-digit millions,” rising to merely $50 million in 2022 and 2023. Her U.S. peak sales estimate landed at $300 million, which is based on a 30% penetration in a subgroup of HFrEF patients that are not optimally managed on Entresto.
Merck views Verquvo’s patient selection criteria not as a “subpopulation,” Joerg Koglin, vice president of global clinical development at the company, said in an email interview. Instead, a worsening event could be a specific “clinical trigger” in a patient’s disease journey. “As such, we believe that Verquvo represents a meaningful addition to the treatment armamentarium for heart failure physicians,” he said.
Verquvo is an sGC stimulator, working on a pathway key in cardiovascular functions. Bayer markets the first sGC stimulator approved in the U.S., Adempas, in pulmonary arterial hypertension.
The drug proved its case in the phase 3 Victoria trial. Compared with placebo, it delivered a 10% relative risk reduction in composite cardiovascular-related death and heart failure hospitalization, according to data presented at the 2020 American College of Cardiology virtual meeting. Industry watchers have picked out some caveats in those data—as well as potential upsides—for Verquvo.
First, some industry opinion leaders saw the 10% improvement as “modest,” according to SVB Leerink analysts. While Victoria enrolled sicker patients than Entresto and Farxiga’s separate trials, “the physicians cautioned against assuming a role for [Verquvo] for severe patients as the benefit of other HF therapies in this population could be just as good or better,” the SVB Leerink team wrote in a July note.
Instead of relative risk reduction, Koglin pointed to the absolute risk reduction. “For patients, physicians and payers, the most relevant efficacy parameter is the absolute risk reduction translating into ‘how many patients do I have to treat with a new therapy to prevent one heart failure hospitalization or CV death,’” which is technically known as the number needed to treat, or NNT, Koglin said. On that marker, Verquvo compares well to other recent heart failure studies, he said.