Assessment Status |
Full HTA submission received from Applicant |
HTA ID |
22064 |
Drug |
Teclistamab |
Brand |
Tecvayli® |
Indication |
As monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 antibody and have demonstrated disease progression on the last therapy. |
Rapid review commissioned |
20/09/2022 |
Rapid review completed |
03/11/2022 |
Rapid review outcome |
A full HTA is recommended to assess the clinical effectiveness and cost effectiveness of teclistamab compared with the current standard of care. |
Full pharmacoeconomic assessment commissioned by HSE |
29/11/2022 |
Pre-submission consultation with Applicant |
24/01/2023 |
Full submission received from Applicant |
18/05/2023 |