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Ravulizumab (new indication: myasthenia gravis, patients who are anti-acetylcholine receptor (AChR) antibody-positive)

 

Subject:

  • Active Substance: Ravulizumab 
  • Name: Ultomiris®
  • Therapeutic area: Myasthenia gravis
  • Pharmaceutical company: Alexion Pharma Germany GmbH

 

Time table:

  • Start: 01.11.2022
  • Publication of assessment: 01.02.2023
  • End of public hearing: 22.02.2023
  • Final decision by G-BA: middle of April 2023

 

Comparative therapy:

  1. Patients who are still eligible for standard therapy: therapy at the physician's discretion
  2. Patients who are not eligible for standard therapy: eculizumab