National Centre for Pharmacoeconomics

National Centre for

NCPE Ireland

Bempedoic acid/Ezetimibe (Nustendi®) HTA ID: 20026b

Bempedoic acid plus ezetimibe is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia, as an adjunct to diet (a) in combination with a statin in patients unable to reach LDL-C goals with the maximum tolerated dose of a statin in addition to ezetimibe (b) alone in patients who are either statin – intolerant or for whom a statin is contraindicated and are unable to reach LDL-C goals with ezetimibe alone and (c) in patients already being treated with the combination of bempedoic acid and ezetimibe as separate tablets with or without a statin.

NCPE Assessment Process Discontinued
Rapid review commissioned 15/06/2020
Rapid review completed 03/07/2020
Rapid Review outcome A full pharmacoeconomic assessment is recommended to assess the clinical effectiveness and cost effectiveness of of bempedoic acid + ezetimibe (Nustendi®) compared with the current standard of care.
Full pharmacoeconomic assessment commissioned by the HSE 06/07/2020
Pre submission consultation with Applicant 22/09/2020
Full HTA submission received from Applicant 30/04/2021
Preliminary review sent to Applicant 22/06/2021
NCPE assessment re-commenced 19/07/2021
NCPE assessment re-commenced 19/07/2021
Factual accuracy sent to Applicant 28/07/2021
HTA assessment discontinued The assessment of bempedoic acid (Nustendi®) has been discontinued at the manufacturers request. The NCPE considers that the cost-effectiveness of bempedoic acid has not be demonstrated and reimbursement is not recommended. 27/08/2021