Observational Study, Use of Canakinumab Administered Subcutaneously in the Treatment COVID-19 Pneumonia

NCT04348448 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2023-07-21

No results posted yet for this study

Summary

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.

Conditions

Interventions

DRUG

Canakinumab 150 MG/ML [Ilaris]

COVID-19

Sponsors & Collaborators

  • AUSL Romagna Rimini

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-02-01
Primary Completion
2020-05-01
Completion
2020-09-01

Countries

  • Italy

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04348448 on ClinicalTrials.gov