FDA — authorised 21 October 2022
- Application: BLA761289
- Marketing authorisation holder: ASTRAZENECA AB
- Local brand name: IMJUDO
- Indication: INJECTABLE — INTRAVENOUS
- Status: approved
FDA authorised IMJUDO on 21 October 2022
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 21 October 2022; FDA authorised it on 10 November 2022; FDA has authorised it.
ASTRAZENECA AB holds the US marketing authorisation.