Vericiguat (Verquvo®). HTA ID: 21027

Assessment Status NCPE Assessment Process Complete
HTA ID 21027
Drug Vericiguat
Brand Verquvo®
Indication For the treatment of symptomatic chronic heart failure in adult patients with reduced ejection fraction who are stabilised after a recent decompensation event requiring intravenous therapy.
Assessment Process
Rapid review commissioned 21/06/2021
Rapid review completed 15/07/2021
Rapid review outcome A full HTA is recommended to assess the clinical effectiveness and cost effectiveness of vericiguat compared with the current standard of care.
Full pharmacoeconomic assessment commissioned by HSE 24/08/2021
Pre-submission consultation with Applicant 20/09/2021
Full submission received from Applicant 21/03/2022
Preliminary review sent to Applicant 09/06/2022
NCPE assessment re-commenced 04/07/2022
Factual accuracy sent to Applicant 12/07/2022
NCPE assessment re-commenced 20/07/2022
NCPE assessment completed 28/07/2022
NCPE assessment outcome The NCPE recommends that vericiguat not be considered for reimbursement*

*This recommendation should be considered while also having regard to the criteria specified in the Health (Pricing and Supply of Medical Goods) Act 2013

Technical Summary

Plain English Summary