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Why choose PRALUENT®?

The usual starting dose for PRALUENT is 75 mg administered subcutaneously once every 2 weeks. Patients requiring larger LDL-C reduction (>60%) may be started on 150 mg once every 2 weeks, or 300 mg once every 4 weeks (monthly), administered subcutaneously.2

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Fast and sustained LDL-C reduction1,2

  • 50-60% LDL-C reduction
  • Maximum effect after 4 weeks
  • Sustained over 4 years
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Significantly reduces the risk of MACE*1,2

  • 15% RRR HR 0.85 (95% CI 0.78, 0.93) P=0.0003(1,6%ARR)
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Demonstrated to get patients to LDL-C goal**3

  • 95% of ACS patients reached LDL-C goal†3
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Established, long-term safety profile1,2

  • Patients followed over 4 years
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Unique once-monthly pen2,4

The long-term efficacy and safety of PRALUENT has been evaluated in an extensive clinical trial programme:

28 global trials
28 global trials
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>32,100 adult patients
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3,000 study centres

The ODYSSEY OUTCOMES trial was a CVOT with ~19,000 very high-CV-risk ACS patients, over 5 years1,2,5,6**

Background: ODYSSEY OUTCOMES aimed to determine whether PRALUENT would improve cardiovascular outcomes after an acute coronary syndrome in patients receiving high-intensity statin therapy.1

Multicentre, double-blind, placebo-controlled, phase 3 trial** N=18,9241

PRALUENT SC Q2W + max tolerated statins (n=9,462)1

PLACEBO SC Q2W + max tolerated statins (n=9,462)1

Primary endpoint:
MACE1

In ODYSSEY OUTCOMES:1

  • Patients with very-high-risk recurrent CV were enrolled, and 100% of patients had an MI or unstable angina
  • Patients received PRALUENT alongside the optimal standard of care - 89% were on high-intensity statins
  • 2.8 years median follow-up, with over 8,000 patients (44%) eligible to be followed for 3–5 years

Primary endpoint: MACE

At 2.8 years (median follow up)1,2
CVOT

15% RRR

Patients eligible for ≥3 years follow-up††7
Post hoc analysis

17% RRR

secondary-endpoints

ODYSSEY OUTCOMES is the longest randomised, placebo-controlled comparison of PCKS9 inhibition to date.1

All primary and secondary end points were adjudicated by physicians who were unaware of the trial-group assignments.1

To adjust for multiplicity, the results of the main secondary end points were tested in hierarchical fashion if the risk of the composite primary end point was found to be significantly lower in the PRALUENT group than in the placebo group.1

PRALUENT demonstrated LDL-C reduction vs placebo1,2§§

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The LDL-C reduction achieved by PRALUENT was proven to be:

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Intensive

50-60% LDL-C reduction relative to placebo1*

* 62.7% LDL-C reduction compared to placebo at 4 months in ODYSSEY OUTCOMES trial. 18,924 patients were included.

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Fast

4 weeks to reach maximum effect2‖‖

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Sustained

4 years of LDL-C reduction1¶¶

LDL-C reduction within ODYSSEY outcomes: on-treatment analysis1

LDL-C-reduction-4-months-outcomes

Making PRALUENT an option for your ACS patients who are at immediate risk of another CV event and need LDL-C reduction that is both fast and sustained.8,9

Reaching LDL-C goal

In patients at very-high-risk and with an LDL-C goal of <55 mg/dL and a reduction of ≥50% from baseline:5

ACS-patients

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<1.4 mmol/L (<55mg/dL)

All-cause mortality

The ODYSSEY OUTCOMES trial also assessed all-cause mortality reduction in patients treated with PRALUENT vs placebo:1,2,10§¶¶

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Overall population‡‡‡

15% RRR

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Continued risk reduction over time in a post hoc analysis:

After ≥3 years¥¥¥,‡‡‡

22% RRR

PRALUENT has established long-term safety profile and experience1,2,7,11

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The safety profile in ODYSSEY OUTCOMES was comparable to placebo and consistent with the overall safety profile described in the phase 3 controlled trials1,2

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Up to 5 years long-term safety – the longest randomised, placebo-controlled comparison of PCSK9 inhibition to date7‖‖‖

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In 2023, approximately 570,000 patients globally have been treated with PRALUENT11§§§

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*P<0.001.1

†New-onset diabetes was defined according to the presence of 1 or more of the following, with confirmation of the diagnosis by blinded external review by experts in the field of diabetes: an adverse event report, a new prescription for diabetes medication, a glycated haemoglobin level of at least 6.5% on 2 occasions (and a baseline level of <6.5%), or a fasting serum glucose level of at least 126 mg/dL (7.0 mmol/L) on 2 occasions (and a baseline level of <126 mg/dL).1

The safety profile in ODYSSEY OUTCOMES was consistent with the overall safety profile described in the phase 3 controlled trials. The only adverse reaction in ODYSSEY OUTCOMES occurring with higher incidence compared to placed was injection site reaction (P<0.001).1,2

PRALUENT: the only PCSK9i with the option of a once-monthly single injection2

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Patient friendly pen2,3

  • Hidden needle
  • Autoinjector with no button to press
  • Self-inject wherever they are
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Self-inject quickly3

  • Delivers the dose in <20 seconds
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The usability and LDL-C reduction of the PRALUENT pen was assessed in the SYDNEY Device trial, and the following information is related to the ease-of-use associated with the PRALUENT pen.3

PRALUENT reaffirmed rapid and sustained LDL-C reduction with the once-monthly pen3

SYDNEY Device (once-monthly pen) Study:

A 16-week multicentre, randomised, open-label study in the US with 69 hypercholesterolaemia patients despite receiving statin with or without other lipid-lowering therapy randomly received supervised, self-administered PRALUENT.3

Patients were randomised to receive either:

  • Self-administered SYDNEY device 1 x 300 mg injection (n=35) or auto injector 2 x 150 mg (n=34)3
  • The primary endpoint was PTC, which was measured at a rate of 0.5% (n=1) (95% CI, 0.0%–3.2%) during unsupervised injections and was not related to the device3****

For their first dose, patients received supervised, self-administered alirocumab 300 mg via 1 x 300 mg injection with the SYDNEY device (n=35) or 2 x 150 mg injections with the currently approved AI (n=34). All continuing patients subsequently received unsupervised, self-administered alirocumab 300 mg Q4W using the SYDNEY device at Weeks 4, 8, and 12.3

Mean LDL-C reduction from baseline at week 4 was 66.2% with the SYDNEY device3

PRALUENT offers you and your patients a user-friendly device3

High patient satisfaction3

Primary endpoint: PTC rate of 0.5% (n=1) (95% CI, 0.0%–3.2%) during unsupervised injection and not related to the device3****

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Patients in the SYDNEY device study reported a
≥9.7/10
satisfaction score with the SYDNEY device3

High patient adherence12

Primary endpoint: PRALUENT was generally well tolerated. The common TEAEs included:13

  • nasopharyngitis (7.8%)
  • myalgia (7.1%)
  • headache (6.2%)
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Adherence over a mean duration of 72.4 weeks††††12

More information

Click a link below to learn more about PRALUENT

What is PRALUENT?

Click here to learn about how PRALUENT works and who it is for

How to use PRALUENT?

Click here to learn more about how PRALUENT should be used

Indication, Dosing, and Footnotes

NAME OF THE MEDICINAL PRODUCT: Praluent 75 mg, 150 mg or 300 mg solution for injection in pre-filled pen. QUALITATIVE AND QUANTITATIVE COMPOSITION: Each single-use pre-filled pen contains 75 mg alirocumab in 1 ml solution, 150 mg alirocumab in 1 ml solution or 300 mg in 2 ml solution. THERAPEUTIC INDICATIONS: Primary hypercholesterolaemia and mixed dyslipidaemia Praluent is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia and in paediatric patients 8 years of age and older with heterozygous familial hypercholesterolaemia (HeFH) as an adjunct to diet: - 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. Established atherosclerotic cardiovascular disease Praluent is indicated in adults with established atherosclerotic cardiovascular disease to reduce cardiovascular risk by lowering LDL-C levels, as an adjunct to correction of other risk factors: - in combination with the maximum tolerated dose of a statin with or without other lipid-lowering therapies or, - alone or in combination with other lipid-lowering therapies in patients who are statin-intolerant, or for whom a statin is contraindicated. POSOLOGY AND METHOD OF ADMINISTRATION: Prior to initiating alirocumab secondary causes of hyperlipidaemia or mixed dyslipidaemia (e.g., nephrotic syndrome, hypothyroidism) should be excluded. The usual starting dose for alirocumab is 75 mg administered subcutaneously once every 2 weeks. Patients requiring larger LDL-C reduction (>60%) may be started on 150 mg once every 2 weeks, or 300 mg once every 4 weeks (monthly), administered subcutaneously. The dose of alirocumab can be individualised based on patient characteristics such as baseline LDL-C level, goal of therapy, and response. Lipid levels can be assessed 4 to 8 weeks after treatment initiation or titration, and dose adjusted accordingly (up-titration or down-titration). If additional LDL-C reduction is needed in patients treated with 75 mg once every 2 weeks or 300 mg once every 4 weeks (monthly), the dosage may be adjusted to the maximum dosage of 150 mg once every 2 weeks. If a dose is missed, the patient should administer the injection as soon as possible and thereafter resume treatment on the original schedule. No dose adjustment is needed for elderly patients, or patients with mild or moderate hepatic or renal impairment, in patients based on weight. Alirocumab has not been studied in paediatric patients less than 8 years of age. Method of administration Subcutaneous injection into the thigh, abdomen or upper arm. Each pre-filled pen is for single use only. To administer the 300 mg dose, either one 300 mg injection or two 150 mg injections should be given consecutively at two different injection sites. It is recommended to rotate the injection site with each injection. Alirocumab should not be injected into areas of active skin disease or injury such as sunburns, skin rashes, inflammation, or skin infections. Alirocumab must not be co-administered with other injectable medicinal products at the same injection site. The patient may either self-inject alirocumab, or a caregiver may administer alirocumab, after guidance has been provided by a healthcare professional on proper subcutaneous injection technique. The solution should be allowed to warm to room temperature prior to use. CONTRAINDICATIONS: Hypersensitivity to the active substance or to any of the excipients. SPECIAL WARNINGS AND PRECAUTIONS FOR USE: Traceability In order to improve the traceability of biological medicinal products, the name and the batch number of the administered product should be clearly recorded. Allergic reactions General allergic reactions, including pruritus, as well as rare and sometimes serious allergic reactions such as hypersensitivity, nummular eczema, urticaria, and hypersensitivity vasculitis have been reported in clinical studies. Angioedema has been reported in the postmarketing setting. If signs or symptoms of serious allergic reactions occur, treatment with alirocumab must be discontinued and appropriate symptomatic treatment initiated. Renal impairment In clinical studies, there was limited representation of patients with severe renal impairment (defined as eGFR < 30 ml/min/1.73 m2). Alirocumab should be used with caution in patients with severe renal impairment. Hepatic impairment Patients with severe hepatic impairment (Child-Pugh C) have not been studied. Alirocumab should be used with caution in patients with severe hepatic impairment. UNDESIRABLE EFFECTS: injection site reactions, upper respiratory tract signs and symptoms, pruritus, urticaria, eczema nummular hypersensitivity. MARKETING AUTHORISATION HOLDER: Sanofi Winthrop Industrie 54, rue La Boétie F-75008 Paris, France. DATE OF REVISION OF THE TEXT: Nov 2024. Medicinal product subject to restricted medical prescription. Detailed information on this medicine is available on European Medicines Agency website http://www.ema.europa.eu.

PRESCRIPTION MEDICATION. ATC-code: C10AX14.Reimbursement: Reimbursed for patients with diagnosed heterozygous familial hypercholesterolemia who, despite maximum tolerable treatment with statin and ezetimibe, have residual LDL cholesterol of 2.6 mmol/L or higher. Reimbursed for patients with diagnosed atherosclerotic cardiovascular disease who, despite maximum tolerable treatment with statin and ezetimibe, have residual LDL cholesterol of 1.8 mmol/L or higher. Reimbursed for patients with diagnosed diabetes mellitus and target organ damage (microalbuminuria, retinopathy, or neuropathy), or at least three major risk factors, or early onset of type 1 diabetes mellitus with long duration, who, despite maximum tolerable treatment with statin and ezetimibe, have residual LDL cholesterol of 2.6 mmol/L or higher. For more information see fass.se(https://www.fass.se/LIF/product?userType=0&nplId=20141231000088). Sanofi AB. Phone +46-8-634 50 00.

Adults2

Prior to initiating PRALUENT® secondary causes of hyperlipidaemia or mixed dyslipidaemia (e.g., nephrotic syndrome, hypothyroidism) should be excluded.

The usual starting dose for alirocumab is 75 mg administered subcutaneously once every 2 weeks. Patients requiring larger LDL-C reduction (>60%) may be started on 150 mg once every 2 weeks, or 300 mg once every 4 weeks (monthly), administered subcutaneously.

The dose of PRALUENT® can be individualised based on patient characteristics such as baseline LDL-C level, goal of therapy, and response. Lipid levels can be assessed 4 to 8 weeks after treatment initiation or titration, and dose adjusted accordingly (up-titration or down-titration).

If additional LDL-C reduction is needed in patients treated with 75 mg once every 2 weeks or 300 mg once every 4 weeks (monthly), the dosage may be adjusted to the maximum dosage of 150 mg once every 2 weeks.

HeFH in paediatric patients 8 years of age and older:2

Body weight of patients Recommended dose Recommended dose if additional LDL-C reduction is needed*
Less than 50 kg 150 mg once every 4 weeks 75 mg once every 2 weeks
50 kg or more 300 mg once every 4 weeks 150 mg once every 2 weeks

If a dose is missed, the dose should be administered as soon as possible and thereafter, dosing should be resumed on the original schedule.

MAT-SE-2400765 v.1.0 02/2025