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10.1080/14656566.2025.2601062

http://scihub22266oqcxt.onion/10.1080/14656566.2025.2601062
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41351386!?!41351386

suck abstract from ncbi

pmid41351386      Expert+Opin+Pharmacother 2025 ; ? (?): ?
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  • Lipoprotein(a) - treatments in development #MMPMID41351386
  • Tomlinson B; Law CF
  • Expert Opin Pharmacother 2025[Dec]; ? (?): ? PMID41351386show ga
  • INTRODUCTION: Lipoprotein(a) [Lp(a)] is established as an independent risk factor for atheromatous cardiovascular disease and aortic valve stenosis. Currently available lipid-lowering pharmacotherapies have limited effects on elevated levels of Lp(a) and several new therapies are in development to lower Lp(a). AREAS COVERED: This article reviews the novel therapies in development to reduce Lp(a) in patients with elevated levels. These were identified by a PubMed search and mainly focus on the drugs that are at an advanced stage of development. EXPERT OPINION: The N-acetylgalactosamine (GalNAc)-conjugated antisense oligonucleotide (ASO) pelacarsen and the small-interfering RNA (siRNA) agents olpasiran, lepodisiran and zerlasiran have all been shown to be safe and effective in lowering Lp(a) levels between 80% and almost 100%. Pelacarsen, olpasiran, and lepodisiran are being tested in phase 3 cardiovascular outcome studies and the first results may be available in 2026. Muvalaplin is a small molecule given orally once daily and reduces Lp(a) by up to 65%. It is also being assessed in a cardiovascular outcome study. It will be essential to identify what baseline level of Lp(a) is needed and what degree of Lp(a) lowering is required to produce a cardiovascular benefit and whether aggressive lowering of Lp(a) has any adverse effects.
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