Inotersen (Tegsedi®)

Inotersen (Tegsedi®) was added to the High Tech Arrangement on 1st October 2022. A Managed Access Protocol (MAP) is in place for Inotersen. This outlines the criteria that must be satisfied in order for a patient to be recommended for reimbursement of Inotersen under the High Tech Arrangement.

The prescribing of Inotersen under the High Tech Arrangement is confined to consultants with experience in the diagnosis and management of hereditary transthyretin-mediated (hATTR) amyloidosis in specialist centre(s) in Ireland, who have agreed to the terms of the MAP and have been approved by the HSE. ​

The clinician must submit an application for individual reimbursement approval for each patient. Applications for individual reimbursement approval will only be considered from approved clinicians.

A copy of the HSE-Managed Access Protocol for Inotersen and the application form for individual reimbursement approval can be found in the Related Files section below.

For further information, please contact