Pricing and Reimbursement Application Tracker
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mirvetuximab soravtansine (Elahere®)
Application Details
HSE Application ID
HSE100008
HTA Number
24051
HTA Link
https://www.ncpe.ie/mirvetuximab-soravtansine-elahere-hta-id-24051/
Drug
mirvetuximab soravtansine
Brand
Elahere®
Applicant
AbbVie
Indication Applied For
As monotherapy indicated for the treatment of adult patients with folate receptor alpha (FRα) positive, platinum-resistant high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who have received one to three prior systemic treatment regimens.
Application Date
19/12/2024
Marketing Authorisation Date
14/11/2024
Application Status
NCPE Assessment Completed
25/06/2026
Full Health Technology Assessment Commissioned by HSE
26/02/2025
Rapid Review Completed
04/02/2025
Pricing and Reimbursement Application Complete
19/12/2024
Rapid Review Commissioned
17/12/2024
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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Application Withdrawn at the Request of Applicant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
Rapid Review Completed: On the basis of current evidence, the NCPE recommends that the product not be considered for reimbursement.
HSE Approval Letter Issued to Applicant
Full Health Technology Assessment Submitted to NCPE
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