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Merck's experimental drug, enlicitide, has shown promising results in reducing LDL cholesterol in a Phase 3 trial. Analysts predict notable upside potential, with a one-year price target averaging $99.66 and a potential 46.68% increase based on GF Value. The drug has a favorable safety profile and Merck plans to initiate regulatory submissions and conference presentations.
Merck (NYSE: MRK), known as MSD outside the United States and Canada, has announced positive topline results from the Phase 3 CORALreef Lipids trial evaluating enlicitide decanoate, an investigational oral proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor. The trial, which enrolled over 1,000 participants with hypercholesterolemia on moderate or high-intensity statins or with documented statin intolerance, met all primary and key secondary endpoints. Enlicitide demonstrated statistically significant and clinically meaningful reductions in low-density lipoprotein cholesterol (LDL-C) compared to placebo at Week 24, as well as reductions in non-HDL-C, apolipoprotein B (ApoB), and lipoprotein(a) [Lp(a)]. The drug also showed a favorable safety profile with no clinically meaningful differences in adverse events between treatment groups.
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