drugset / Trial / NCT04594343
Clinical Study to Evaluate the Effects of Disulfiram in Patients With Moderate COVID-19
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This clinical trial evaluates the safety, efficacy, and biomarker levels of FDA-approved drug disulfiram in the treatment of adult subjects hospitalized with moderate COVID-19. Disulfiram may limit the hyperinflammatory response associated with COVID-19 and reduce the risk of progression to severe illness. Subjects will be screened and randomized to receive either daily administration of oral disulfiram or placebo for 14 days. Subjects will be followed up on Day 28.
Timeline
- Start
- 2020-11-20
- Primary completion
- 2021-09-10
- Completion
- 2021-09-25
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Disulfiram | Small molecule | 500 mg | Oral |