Official Title
Efficacy of Anakinra in the Management of Patients With COVID-19 Infection in Qatar: A Randomized Clinical Trial
Brief Summary

Coronavirus Disease 2019 (COVID-19) was first isolated in Wuhan, China in December 2019. It is rapidly spreading worldwide, posing a severe threat to global health. Many therapeutics have been investigated for the treatment of this disease with inconclusive outcomes. Anakinra - an interleukin (IL)-1 receptor antagonist - had showed survival benefits in patients with macrophage activation syndrome (MAS) and sepsis and was investigated for the use in COVID-19 infection with promising outcomes.

Completed
COVID19
Pneumonia
Cytokine Release Syndrome
Corona Virus Infection
Viral Infection

Drug: Anakinra

Patient will receive Anakinra 100 mg SC injection every 12 hours for 3 days, then 100 mg once daily from day 4 to day 7 plus Standard of Care
Other Name: Kineret®

Other: Standard of Care

Patients will receive the Standard of Care therapy as per the local treatment protocol

Eligibility Criteria

Inclusion criteria:

- Hospitalized adult (age ≥ 18yrs)

- Confirmed COVID-19 diagnosis

- Presence of respiratory distress in addition to signs of cytokine release syndrome

- Radiological evidence of pneumonia

- Signed informed consent

Exclusion Criteria:

- Known allergic reactions to the study medication or any component of the product.

- Active bacterial, viral, TB, fungal infectious diseases

- Received immunosuppressant or immunomodulatory in the past 30 days

- Neutrophil count < 500 cells/microliter

- Platelets < 50,000/microliter

- Pregnant or breastfeeding females

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
Qatar
Locations

Hamad Medical Corporation
Doha, Qatar

Hamad Medical Corporation
NCT Number
MeSH Terms
Infections
Communicable Diseases
COVID-19
Virus Diseases
Coronavirus Infections
Cytokine Release Syndrome
Interleukin 1 Receptor Antagonist Protein