A new oral medication to reduce LDL cholesterol has shown exceptional promise in a recent medical study, marking a potential breakthrough for patients with heterozygous familial hypercholesterolemia (HeFH). The findings, published in the Journal Of The American Medical Association (JAMA), reveal that Merck’s experimental drug Enlicitide reduced bad cholesterol levels by nearly 60%, positioning it as a major advancement in cardiovascular care.
Enlicitide belongs to the class of PCSK9 inhibitors, which until now have only been available as injections. By formulating the therapy as a pill for the first time, researchers aim to offer patients a more convenient and accessible pathway to manage genetically driven high cholesterol.
Heterozygous familial hypercholesterolemia affects approximately one in 250 people due to a mutation that limits the body’s ability to clear LDL cholesterol from the bloodstream. As LDL builds up in arteries, the risk of early heart disease and stroke increases significantly. Despite the availability of statins and other therapies, many HeFH patients struggle to achieve target LDL levels.
Enlicitide works by binding to PCSK9 proteins in the blood and protecting liver receptors responsible for clearing LDL cholesterol. By preserving these receptors, the liver can remove more LDL cholesterol, resulting in a substantial reduction of harmful levels in the bloodstream. This needle-free formulation represents a major shift in cholesterol treatment and could greatly improve adherence among patients who prefer oral medication.
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