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Zanubrutinib (new indication: marginal zone lymphoma (MLZ), ≥ 1 prior anti-CD20-antibody-based therapy)

 

Subject:

  • Active Substance: Zanubrutinib
  • Name: Brukinsa®
  • Therapeutic area: Marginal zone lymphoma (MZL)
  • Pharmaceutical company: BeiGene Germany GmbH

 

Time table:

  • Start: 15.12.2022
  • Publication of assessment: 15.03.2023
  • End of public hearing: 05.04.2023
  • Final decision by G-BA: middle of June 2023

 

Comparative therapy:

  • A patient-individual therapy depending on previous therapies, disease course (including duration of remission since last therapy) and general condition