FDA — authorised 12 September 2024
- Application: BLA761347
- Marketing authorisation holder: GENENTECH INC
- Local brand name: TECENTRIQ HYBREZA
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Atezolizumab and Recombinant Human Hyaluronidase on 12 September 2024
Yes. FDA authorised it on 12 September 2024.
GENENTECH INC holds the US marketing authorisation.