[A22-47] Casirivimab/imdevimab (post-exposure prophylaxis of COVID-19) – Benefit assessment according to §35a Social Code Book V

Last updated 15.07.2022

Project no.:
A22-47

Commission:
Commission awarded on 19.04.2022 by the Federal Joint Committee (G-BA).

Report type:
Dossier assessment

Status:
Commission completed

Department/Division:
Drug Assessment

Topic:
Immune system and infections

Indication:

Post-exposure prophylaxis for COVID-19 in adults and adolescents aged 12 years and older and with a body weight of at least 40 kg

Result of dossier assessment:
  • Without complete immunisation, negative SARS-CoV-2 RT-qPCR test: hint of considerable added benefit
  • Without complete immunisation, positive SARS-CoV-2 RT-qPCR test: hint of minor added benefit
  • With complete immunisation: added benefit not proven
Note:

After completion of the assessment by IQWiG the Federal Joint Committee (G-BA) conducts a commenting procedure. This may provide supplementary information and as a result lead to a modified benefit assessment. Further information and the decision on the early benefit assessment can be found on the relevant page of the G-BA website.

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