FDA — authorised 18 March 2022
- Application: BLA761234
- Marketing authorisation holder: BRISTOL MYERS SQUIBB
- Local brand name: OPDUALAG
- Indication: SOLUTION — INTRAVENOUS
- Status: approved
FDA authorised Relatilmab on 18 March 2022
Yes. FDA authorised it on 18 March 2022.
BRISTOL MYERS SQUIBB holds the US marketing authorisation.