drugset / Trial / NCT04329572

Efficacy and Safety of Hydroxychloroquine and Azithromycin for Patients With Moderate to Severe COVID-19

NCT04329572 ↗

Phase 0 Suspended 400 enrolled Azidus Brasil
NaSingle-groupOpen-labelTreatment

Summary

This is an exploratory study to evaluate the efficacy of hydroxychloroquine (400 mg BID on D1 and 400 mg/day on D2 to D5) and azithromycin (500 mg/ 5 days) to treat moderate to severe COVID-19 pneumonia.

Timeline

Start
2020-04-23
Primary completion
2020-05-31
Completion
2023-06-30

Outcome

Outcome not reported

Stopped: “Azidus, the CRO hired for this study by Prevent Senior has lost the interest to conduct this study.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Azithromycin Small molecule 500 mg —
Subject Hydroxychloroquine Small molecule 400 mg —

Indications