🇺🇸 Proactive TDM-based dosing of ixekizumab in United States

FDA authorised Proactive TDM-based dosing of ixekizumab on 22 March 2016

Marketing authorisation

FDA — authorised 22 March 2016

  • Application: BLA125521
  • Marketing authorisation holder: ELI LILLY AND CO
  • Local brand name: TALTZ
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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Proactive TDM-based dosing of ixekizumab in other countries

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

Other Immunology approved in United States

Frequently asked questions

Is Proactive TDM-based dosing of ixekizumab approved in United States?

Yes. FDA authorised it on 22 March 2016.

Who is the marketing authorisation holder for Proactive TDM-based dosing of ixekizumab in United States?

ELI LILLY AND CO holds the US marketing authorisation.