Pricing and Reimbursement Application Tracker
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rucaparib (Rubraca®)
Application Details
HSE Application ID
HSE100020
HTA Number
25011
HTA Link
https://www.ncpe.ie/rucaparib-rubraca-hta-id-25011/
Drug
rucaparib
Brand
Rubraca®
Applicant
pharmaand GmbH
Indication Applied For
Indicated as monotherapy for the maintenance treatment of adult patients with advanced (FIGO Stages III and IV) high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy.
Application Date
20/02/2025
Marketing Authorisation Date
15/11/2023
Application Status
Applicant Meeting Held with CPU
08/05/2025
Awaiting Proposal from Applicant
08/05/2025
Rapid Review Completed
24/03/2025
Pricing and Reimbursement Application Complete
20/02/2025
Rapid Review Commissioned
17/02/2025
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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Application Withdrawn at the Request of Applicant
HSE Approval Letter Issued to Applicant
Full Health Technology Assessment Submitted to NCPE
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