The study is configured as a retrospective and prospective observational study. The study will be multi-center and will involve all COVID-19 pneumonia patients treated with canakinumab administered subcutaneously.
Drug: Canakinumab 150 MG/ML [Ilaris]
COVID-19
Inclusion Criteria:
- patients with COVID 19 who have received or are candidates to receive treatment with
canakinumab subcutaneously
- Age> 18 years
- Pneumonia diagnosed with Chest X-ray / or Chest CT
Exclusion Criteria:
- Patients with Covid19-related pathology in the context of another cause of major
admission (trauma, surgery)