Ocrelizumab subcutaneous (Ocrevus SC®). HTA ID: 25015

Assessment Status Rapid Review Complete
HTA ID 25015
Drug Ocrelizumab
Brand Ocrevus SC®
Indication Ocrelizumab SC is indicated • For the treatment of adult patients with relapsing forms of multiple sclerosis (RMS) with active disease defined by clinical or imaging features. • For the treatment of adult patients with early primary progressive multiple sclerosis (PPMS) in terms of disease duration and level of disability, and with imaging features characteristic of inflammatory activity.
Assessment Process
Rapid review commissioned 18/02/2025
Rapid review completed 20/03/2025
Rapid review outcome A full HTA is not recommended. The NCPE recommends that ocrelizumab SC not be considered for reimbursement at the submitted price*.

*This recommendation should be considered while also having regard to the criteria specified in the Health (Pricing and Supply of Medical Goods) Act 2013.

 

Next steps: The NCPE Assessment Report and recommendation, will be considered by the HSE when making their decision on reimbursement, while also having regard to the criteria specified in the Health (Pricing and Supply of Medical Goods) Act 2013.

Further information on this process may be found here.

Further information on the status of this decision may be found here.