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dostarlimab (Jemperli®)
Application Details
HSE Application ID
HSE100106
HTA Number
26020
HTA Link
https://www.ncpe.ie/dostarlimab-jemperli-hta-id-26020/
Drug
dostarlimab
Brand
Jemperli®
Applicant
GlaxoSmithKline Limited
Indication Applied For
Dostarlimab in combination with carboplatin and paclitaxel indicated for the first-line treatment of adult patients with primary advanced or recurrent endometrial cancer (EC) and who are candidates for systemic therapy. This application focuses on a subgroup of patients with recurrent or advanced deoxyribonucleic acid (DNA) mismatch repair proficient (MMRp) or microsatellite-stable (MSS) EC who are candidates for systemic therapy.
Application Date
07/05/2026
Marketing Authorisation Date
15/01/2025
Application Status
Full Health Technology Assessment Commissioned by HSE
22/05/2026
Rapid Review Completed
21/05/2026
Pricing and Reimbursement Application Complete
07/05/2026
Rapid Review Commissioned
06/05/2026
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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Application Withdrawn at the Request of Applicant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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