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