Muvalaplin, an oral drug, offers the path-breaking world’s first treatment for lipoprotein(a), a bad cholesterol that increases the risk of heart attack and stroke.
A novel medicine, muvalaplin provides a ground-breaking, world’s first-ever treatment for lipoprotein(a), a predisposed form of cholesterol that raises the risk of heart attack and stroke. This landmark research and trial was //led by Professor Stephen Nicholls, Director of the Monash University’s Victorian Heart Institute and Victorian Heart Hospital and presented at the European Society of Cardiology Congress in Amsterdam and published in JAMA(1✔ ✔Trusted Source
Muvalaplin, an Oral Small Molecule Inhibitor of Lipoprotein(a) FormationA Randomized Clinical Trial
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Unraveling The Role of Lipoprotein(a) in Heart Health
High levels of Lipoprotein(a), known as Lp(a) or spoken as ‘LP little a’, impact one in five people globally with no approved treatment currently on the market.‘Muvalaplin is a gamechanger in not only lowering the bad cholesterol, but being able to deliver it in an oral tablet means it will be more accessible for patients. #muvalplin #curbbadcholestrol #healthyheart’
The trial demonstrated the success of Muvalaplin - the first oral drug ever developed to target Lp(a) - effectively lowering levels by up to 65%. It works by disrupting the ability of Lp(a) to form in the body.Lp(a) is similar to LDL cholesterol, sometimes called ‘bad cholesterol’, but is more sticky, increasing the risk of blockages and blood clots in arteries. Common LDL-lowering drugs such as statins don’t have the same lowering effect on Lp(a). Being largely genetic, Lp(a) is also difficult to control through diet, exercise and other lifestyle changes.
Although Lp(a) was discovered nearly 60 years ago there still aren’t any widely accessible treatments available to lower levels and reduce cardiovascular risk.
Professor Nicholls said the global research industry has been working on a targeted solution to treat elevated Lp(a) for the past decade, but advancements so far have made it difficult to administer injection-based therapies that are not yet on the market.
“When it comes to treating high Lp(a), a known risk factor for cardiovascular disease, our clinicians currently have no effective tools in their kit,” Professor Nicholls said.“Lp(a) is essentially a silent killer with no available treatment, this drug changes that.”
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Reference:
- Muvalaplin, an Oral Small Molecule Inhibitor of Lipoprotein(a) FormationA Randomized Clinical Trial- (https://jamanetwork.com/journals/jama/fullarticle/2808864)