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Not Yet RecruitingNCT06817096

Efficacy and Safety of Nitazoxanide 600 Mg in the Outpatient Treatment of COVID-19 and Influenza

Phase 3, Multicenter, Parallel, Randomized, Single-blind, Placebo-controlled Clinical Trial to Evaluate the Efficacy and Safety of Nitazoxanide 600 Mg Administered Twice Daily, in the Outpatient Treatment of COVID-19 and Influenza

Status
Not Yet Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
340 (estimated)
Sponsor
Azidus Brasil · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

2\. Participants will: * Take nitazoxanide 600mg (or placebo) orally twice daily for 7 days, for a total of 14 doses. * Visit the clinic on the 7th day of treatment for a check-up and safety tests. * Keep a diary of their symptoms and other medications used

Conditions

Interventions

TypeNameDescription
DRUGNitazoxanide 600Mg Oral Tablet / placebo oral tablet1 tablet every 12 hours

Timeline

Start date
2025-02-01
Primary completion
2026-12-01
Completion
2027-06-01
First posted
2025-02-10
Last updated
2025-02-10

Source: ClinicalTrials.gov record NCT06817096. Inclusion in this directory is not an endorsement.

Efficacy and Safety of Nitazoxanide 600 Mg in the Outpatient Treatment of COVID-19 and Influenza (NCT06817096) · Clinical Trials Directory