Subject:
- Active Substance: Sotrovimab
- Name: Xevudy®
- Therapeutic area: Coronavirus disease 2019 (COVID-19)
- Pharmaceutical company: GlaxoSmithKline GmbH & Co. KG
Time table:
- Start: 15.05.2022
- Final decision by G-BA: 03.11.2022
Final decision:
- Adult patients with COVID-19 disease who do not require supplemental oxygen therapy and who are at increased risk for a severe course of COVID-19 in the case of infection with an infection with a viral variant against which sotrovimab has significantly reduced or insufficient efficacy: No additional benefit proved
- Adult patients with COVID-19 disease who do not require supplemental oxygen therapy and who are at increased risk for a severe course of COVID-19 in the case of infection with an infection with a viral variant against which sotrovimab has sufficient efficacy: Hint for a considerable additional benefit
- Adolescents from 12 to < 18 years of age with at least 40 kg body weight with COVID-19 disease who do not require supplemental oxygen therapy and are at increased risk for a severe course of COVID-19: No additional benefit proved