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Lonafarnib (Zokinvy®)
Application Details
HSE Application ID
HSE100077
HTA Number
25063
HTA Link
https://www.ncpe.ie/lonafarnib-zokinvy-hta-id-25063/
Drug
Lonafarnib
Brand
Zokinvy®
Applicant
Sentynl Therapeutics
Indication Applied For
Indicated for the treatment of patients 12 months of age and older with a genetically confirmed diagnosis of Hutchinson-Gilford Progeria syndrome or a processing-deficient progeroid laminopathy associated with either a heterozygous LMNA mutation with progerin-like protein accumulation or a homozygous or compound heterozygous ZMPSTE24 mutation.
Application Date
28/10/2025
Marketing Authorisation Date
18/07/2022
Application Status
Rapid Review Completed
27/11/2025
Rapid Review Commissioned
28/10/2025
Pricing and Reimbursement Application Complete
28/10/2025
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Status
Pricing and Reimbursement Application Complete
Rapid Review Commissioned
Rapid Review Completed
Applicant Meeting Held with CPU
Awaiting Proposal from Applicant
Proposal from Applicant Under Review
Full Health Technology Assessment Commissioned by HSE
NCPE Assessment Completed
HSE Drugs Group Review Pending
Reviewed by HSE Drugs Group
HSE Rare Disease Technology Review Committee - Review Requested
HSE Rare Disease Technology Review Committee - Review Received
Further Information Requested by HSE Drugs Group
Reviewed by HSE Senior Leadership Team
Managed Access Protocol (MAP) Commissioned
Proposed HSE Decision Issued to Applicant
Applicant Representations Received
HSE Decision Issued to Applicant
Application On Hold at the Request of Applicant
Application Withdrawn at the Request of Applicant
Application on Hold as Agreed by HSE and Applicant
HSE Approval Letter Issued to Applicant
Full Health Technology Assessment Submitted to NCPE
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