drugset / Trial / NCT04403243
COLchicine Versus Ruxolitinib and Secukinumab in Open-label Prospective Randomized Trial in Patients With COVID-19
Phase 2
Completed
70 enrolled
Lomonosov Moscow State University Medical Research and Educational Center
RandomizedParallel-groupOpen-labelTreatment
Summary
Patients with mild and severe coronavirus disease 2019 (COVID 19) will be randomized 3:1:1:3 into four groups: colchicine, ruxolitinib, secukinumab, and control groups. . Patients will be follow-up during 45 days after randomization. Change in clinical assessment score COVID 19 (CAS COVID 19) between baseline and 12th day will be evaluated as the primary endpoint. Risk of death or mechanical ventilation during 45 days after randomization will also be assessed
Timeline
- Start
- 2020-05-08
- Primary completion
- 2020-07-22
- Completion
- 2020-08-23
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Colchicine | Small molecule | 0.5 mg | Oral |
| Subject | Ruxolitinib | Small molecule | 5 mg | Oral |
| Subject | Secukinumab | Monoclonal antibody | 300 mg | Subcutaneous |