Trials / Completed
CompletedNCT04643678
Anakinra in the Management of COVID-19 Infection
Efficacy of Anakinra in the Management of Patients With COVID-19 Infection in Qatar: A Randomized Clinical Trial
- Status
- Completed
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Hamad Medical Corporation · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| 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 | Standard of Care | Patients will receive the Standard of Care therapy as per the local treatment protocol |
Timeline
- Start date
- 2020-10-30
- Primary completion
- 2021-03-01
- Completion
- 2021-04-30
- First posted
- 2020-11-25
- Last updated
- 2022-08-16
Locations
1 site across 1 country: Qatar
Source: ClinicalTrials.gov record NCT04643678. Inclusion in this directory is not an endorsement.