Leqvio (inclisiran) vs Evkeeza (evinacumab)

Leqvio (inclisiran) vs Evkeeza (evinacumab)

Leqvio (inclisiran) is a small interfering RNA (siRNA) therapy that works by targeting and silencing specific RNA molecules involved in the production of LDL cholesterol, thereby reducing LDL cholesterol levels in the blood. Evkeeza (evinacumab) is a monoclonal antibody that targets and inhibits the protein ANGPTL3, which plays a role in lipid metabolism, leading to lowered levels of LDL cholesterol and other lipids. When deciding between Leqvio and Evkeeza, a patient should consider factors such as their specific lipid profile, underlying health conditions, the mechanism of action of each medication, and the guidance of their healthcare provider, as these medications are used for different indications and have distinct administration schedules and potential side effects.

Difference between Leqvio and Evkeeza

Metric Leqvio (inclisiran) Evkeeza (evinacumab)
Generic name Inclisiran Evinacumab
Indications Hypercholesterolemia, Heterozygous Familial Hypercholesterolemia (HeFH) Homozygous Familial Hypercholesterolemia (HoFH)
Mechanism of action Small interfering RNA (siRNA) targeting PCSK9 Monoclonal antibody targeting angiopoietin-like 3 (ANGPTL3)
Brand names Leqvio Evkeeza
Administrative route Subcutaneous injection Intravenous infusion
Side effects Injection site reactions, joint pain, urinary tract infections, diarrhea, chest pain, shortness of breath Flu-like symptoms, nausea, dizziness, nosebleeds, allergic reactions
Contraindications Active liver disease, history of a serious hypersensitivity reaction to inclisiran None known
Drug class PCSK9 inhibitor Lipoprotein lipase enhancer
Manufacturer Novartis Regeneron Pharmaceuticals

Efficacy

Leqvio (Inclisiran) for Hypercholesterolemia

Leqvio (inclisiran) is a novel medication approved for the treatment of hypercholesterolemia, specifically in individuals who have elevated low-density lipoprotein cholesterol (LDL-C) levels despite maximally tolerated statin therapy. Inclisiran is a small interfering RNA (siRNA) therapeutic agent that targets the production of the PCSK9 protein in the liver, which plays a significant role in the regulation of LDL-C levels. By reducing the production of PCSK9, Leqvio effectively lowers LDL-C levels. Clinical trials have demonstrated that Leqvio can significantly reduce LDL-C levels by up to 50% when used in addition to statins and other lipid-lowering therapies.

Efficacy of Leqvio in Clinical Trials

The efficacy of Leqvio has been evaluated in several pivotal Phase III trials, including the ORION-9, ORION-10, and ORION-11 studies, which collectively enrolled thousands of patients with atherosclerotic cardiovascular disease (ASCVD) or ASCVD-risk equivalents, and familial hypercholesterolemia. These trials showed that Leqvio administered subcutaneously twice a year after an initial dose and a second dose at three months led to significant and sustained reductions in LDL-C levels. The reduction in LDL-C was maintained throughout the six-month dosing interval, showcasing the long-term benefits of the treatment.

Evkeeza (Evinacumab) for Hypercholesterolemia

Evkeeza (evinacumab) is a monoclonal antibody designed to treat hypercholesterolemia in patients with homozygous familial hypercholesterolemia (HoFH), a rare genetic condition that leads to extremely high levels of LDL-C. Evinacumab works by binding to and inhibiting the function of angiopoietin-like 3 (ANGPTL3), a protein that affects lipid metabolism in the liver. Unlike statins and PCSK9 inhibitors, evinacumab's mechanism of action does not rely on the LDL receptor pathway, making it an effective option for patients with HoFH who have limited or no LDL receptor function.

Effectiveness of Evkeeza in Clinical Studies

The efficacy of Evkeeza was demonstrated in a Phase III trial involving patients with HoFH. The study reported that treatment with evinacumab led to a significant reduction in LDL-C levels compared to placebo, with some patients experiencing a reduction of more than 50%. This reduction was observed irrespective of patients' baseline LDL-C levels or genetic mutations, highlighting the potential of Evkeeza as a treatment for patients with this challenging and severe form of hypercholesterolemia.

Regulatory Agency Approvals

Leqvio
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Evkeeza
  • Food and Drug Administration (FDA), USA

Access Leqvio or Evkeeza today

If Leqvio or Evkeeza are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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