Prescribing information

 

LEQVIO®▼ (inclisiran) is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia, as an adjunct to diet:2,3

  • in combination with a statin or statin with other lipid-lowering therapies in patients unable to reach LDL-C goals with the maximum tolerated dose of a statin, or
  • alone or in combination with other lipid-lowering therapies in patients who are statin-intolerant, or for whom a statin is contraindicated.

 

For full safety information, please refer to the GB and NI Summary of Product Characteristics.

The effect of LEQVIO® on cardiovascular morbidity and mortality has not been determined.2,3

 

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The burden of CVD

The number of people dying prematurely from cardiovascular disease is on the rise for the first time in 50 years,4 showing how urgent it is to act now.

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8 in 10 premature deaths from cardiovascular disease could be prevented by addressing modifiable risk factors5

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Long-term exposure to persistently high LDL-C causes ASCVD and associated cardiovascular events6

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Healthcare costs for CVD in England are estimated at £7.4 billion per year5

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CVD mortality rates are strongly associated with social deprivation7

 

LDL-C management

Why does LDL-C lowering matter?

Abnormal lipid level is the most significant modifiable factor in the risk of a myocardial infarction. Restoring normal lipid levels should therefore be considered as soon as possible to help reduce CVD risk.6

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Each 1 mmol/L LDL-C reduction is associated with a 21% relative lower risk of major vascular events (RR=0.79, 95% CI: 0.77–0.81, p<0.0001)*8

The 2023/2024 QOF recognises the importance of proactive cholesterol management for patients who have already had a cardiovascular event9

Unmet needs in LDL-C lowering

Although LDL-C lowering medications are available, many patients at risk of CVD are unable to reach their optimal LDL-C level.10

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Only 24% of patients with cardiovascular disease are currently reaching the <1.8mmol/L LDL-C target.†1

*Based on a meta-analysis of data from randomised statin trials over an average of 4.9 years (N=174,149 patients). The estimated absolute reduction in major vascular events in participants with a 5-year risk <10% was around 11 per 1,000 over 5 years for each 1.0 mmol/L LDL-C reduction. Major vascular events include fatal myocardial infarction or fatal stroke.8
National CVDPREVENT data covering the period up to March 2022. Data was received from 96.6% of GP practices, including approximately 18 million patients.1

ASCVD, atherosclerotic cardiovascular disease; CVD, cardiovascular disease; LDL-C, low-density lipoprotein cholesterol; NHS, National Health Service; QOF, quality and outcomes framework.

References:

  1. Healthcare Quality Improvement Partnership. Third annual audit report. Available at: https://www.hqip.org.uk/wp-content/uploads/2023/03/Ref-376-CVDPREVENT-Th... [Accessed October 2023]. 
  2. LEQVIO® Great Britain. Summary of Product Characteristics.
  3. LEQVIO® Northern Ireland. Summary of Product Characteristics.
  4. Heart UK. Prioritising the prevention of cardiovascular disease. Available at:  https://​www.heartuk.org.uk/downloads/health-professionals/heart-uk-cvd-preventio... [Accessed October 2023].
  5. The King’s Fund. Cardiovascular disease in England. Available at: https://​​www.kingsfund.org.uk/sites/default/files/2022-11/CVD_Report_Web.pdf [Accessed October 2023].
  6. Ference BA, et al. Eur Heart J 2017;38(32):2459–2472.
  7. UK Health Security Agency. Health Matters: Ambitions to tackle persisting inequalities in cardiovascular disease. Available at: https://​ukhsa.blog.gov.uk/2019/03/04/health-matters-ambitions-to-tackle-persisting-inequalities-in-cardiovascular-disease/ [Accessed October 2023].
  8. CTT Collaborators. Lancet 2012;380(9841):581–590.
  9. National Health Service. Quality and Outcomes Framework guidance for 2023/24. Available at:  https://www.england.nhs.uk/wp-content/uploads/2023/03/PRN00289-quality-a... [Accessed October 2023].
  10. Ray KK, et al. Lancet 2023;29:100624.

LEQVIO® and the LEQVIO® logo are registered trademarks of Novartis AG. Licensed from Alnylam Pharmaceuticals, Inc.

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UK | November 2023 | 301963

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Novartis via uk.patientsafety@novartis.com or online through the pharmacovigilance intake (PVI) tool at www.novartis.com/report
If you have a question about the product, please contact Medical Information on 01276 698370 or by email at medinfo.uk@novartis.com