Regeneron Takes Aim at Amgen and Esperion Therapeutics

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Almost one year after competitor Amgen, Inc. (NASDAQ: AMGN) reported that its cholesterol-lowering drug, Repatha, reduced the risk of major adverse cardiac events (MACE), Regeneron Pharmaceuticals (NASDAQ: REGN) and Sanofi (NYSE: SNY) unveiled similarly strong data this week for their cholesterol drug, Praluent.

Praluent not only reduced the risk of major events, including heart attack and stroke, but it also improved all-cause mortality, which is something Repatha didn't achieve in its study. Regeneron Pharmaceuticals plans to leverage this data to increase sales, including significantly reducing Praluent's price to insurers willing to ease reimbursement requirements. The price cut may help Praluent outcompete Repatha, and potentially, it could help Praluent defend itself if Esperion Therapeutics' (NASDAQ: ESPR) bempedoic acid eventually wins FDA approval.

An important win

Cholesterol-lowering statins are among the most commonly prescribed drugs in the United States, but despite their widespread use, the Centers for Disease Control and Prevention report that an estimated 600,000 Americans still die from heart disease every year.

Three arrows in the bulls eye of a target.
Three arrows in the bulls eye of a target.

IMAGE SOURCE: GETTY IMAGES.

Statins effectively control elevated LDL-C in many patients, but there are still millions of people who don't respond adequately to them or who are unable to take them because of side effects. It's primarily this tough-to-treat population that Amgen and Regeneron Pharmaceuticals' cholesterol drugs are targeting.

Unlike statins that reduce cholesterol production in the liver by targeting the HMG-CoA reductase enzyme, Praluent and Repatha inhibit the PCSK9 protein that's responsible for breaking down LDL-C receptors in the liver. Since PCSK9 inhibitors work differently from statins, they can be used in addition to statins or as an alternative to them. In clinical trials, adding Repatha and Praluent to statin therapy reduced elevated LDL-C by about an additional 60%. Following that performance, the FDA approved both Repatha and Praluent in 2015 within months of each other.

There's no doubt that PCSK9 inhibitors effectively reduce cholesterol, but that hasn't stopped insurers from creating barriers to access to prevent all but the most stubborn cases. Payers' resistance to reimbursing for this class of drugs, however, began to ease after Amgen reported results from Repatha's cardiovascular outcomes study in March 2017.

Repatha didn't meet the cut-off for a statistically significant improvement in all-cause mortality in this trial, but it did cut the risk of hospitalization for unstable angina, coronary revascularization, heart attack, stroke, or cardiovascular death by 15%. Also, the risk of heart attack, stroke, and coronary revascularization, specifically, fell by 27%, 21%, and 22% in the study, respectively.