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Study to Evaluate the Efficacy of COVID19-0001-USR in Patients With Mild/or Moderate COVID-19 Infection in Outpatient — COVID-19  

SARS-CoV-2 Infection Clinical Trial

Official title:
A Two-arm Randomized Double-blind Study With COVID19-0001-USR Administered Via Nebulization to Patients With Mild and/or Moderate Severe Acute Respiratory Syndrome (SARS-COV-2) Infection to Decrease Viral Load

Clinical Trial Summary

Determine the efficacy and safety of COVID19-0001-USR in the treatment of SARS-COV-2 infection in mild to moderate manifestations administered via nebulization/inhalation.

Clinical Trial Description

This is an interventional, randomized controlled, double-blind study (i.e., active and passive control), 1 intervention group will be randomized with COVID 19-001-USR, and a control group to receive a placebo intervention to assess efficacy, tolerance, and decrease viral load and clinical manifestation on patients infected with SARS-COV-2. This will be a self-administered study drug 3 times a day for 7 days ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04595136
Study type Interventional
Source United Medical Specialties
Contact Carlos A Riveros, MD
Phone 305-224-2201
Email Carlosrivg@gmail.com
Status Recruiting
Phase Phase 1/Phase 2
Start date November 2, 2020
Completion date August 30, 2021
View Details
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