🇺🇸 IMJUDO in United States

FDA authorised IMJUDO on 21 October 2022

Marketing authorisations

FDA — authorised 21 October 2022

  • Application: BLA761289
  • Marketing authorisation holder: ASTRAZENECA AB
  • Local brand name: IMJUDO
  • Indication: INJECTABLE — INTRAVENOUS
  • Status: approved

Read official source →

FDA — authorised 10 November 2022

  • Application: BLA761270
  • Marketing authorisation holder: ASTRAZENECA AB
  • Local brand name: IMJUDO
  • Indication: INJECTABLE — INTRAVENOUS
  • Status: approved

Read official source →

FDA

  • Status: approved

IMJUDO in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Oncology approved in United States

Frequently asked questions

Is IMJUDO approved in United States?

Yes. FDA authorised it on 21 October 2022; FDA authorised it on 10 November 2022; FDA has authorised it.

Who is the marketing authorisation holder for IMJUDO in United States?

ASTRAZENECA AB holds the US marketing authorisation.