drugset / Trial / NCT04427098
Enoxaparin in COVID-19 Moderate to Severe Hospitalized Patients
Non-randomizedParallel-groupOpen-labelTreatment
Summary
General objective of the study To assess the efficacy and safety of enoxaparin in hospitalized patients with moderate to severe COVID-19 (Coronavirus Disease 2019) infection. Study Design The study consists of two parts: * a phase II single-arm interventional prospective study including all patients treated with the study drug; * an observational prospective cohort study including all patients screened for receiving the study drug but not included in the phase II study. Patients will be enrolled from "date of study approval" for 1 month. Each patient will be followed-up for a minimum of 90 days after COVID19 diagnosis.
Timeline
- Start
- 2020-05-22
- Primary completion
- 2021-09-29
- Completion
- 2021-09-29
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Enoxaparin sodium | Other / unclassified | 40 mg | Subcutaneous |
| Comparator | Enoxaparin sodium | Other / unclassified | 60 mg | Subcutaneous |
| Comparator | Enoxaparin sodium | Other / unclassified | 80 mg | Subcutaneous |
| Comparator | Enoxaparin sodium | Other / unclassified | 100 mg | Subcutaneous |