Subject:
- Active Substance: Zanubrutinib
- Name: Brukinsa®
- Therapeutic area: Chronic lymphocytic leukemia (CLL)
- Pharmaceutical company: BeiGene Germany GmbH
Time table:
- Start: 15.12.2022
- Final decision by G-BA: 15.06.2023
Final decision:
- Patients without genetic risk factors for whom therapy with FCR is not suitable: Hint of minor additional benefit
- Patients with risk factors and patients without risk factors for whom therapy with FCR is suitable: No additional benefit proved