Niclosamide for Mild to Moderate COVID-19

PHASE2CompletedINTERVENTIONAL
Enrollment

73

Participants

Timeline

Start Date

October 1, 2020

Primary Completion Date

April 20, 2021

Study Completion Date

August 19, 2021

Conditions
COVID-19
Interventions
DRUG

Niclosamide

Participants in the treatment arm will receive Niclosamide 2 grams orally once daily for 7 days in addition to current standard of care treatment. Oropharyngeal swab samples will be collected for viral shedding as measured by PCR on days 3, 7, 10, 14. Fecal samples will be collected for viral shedding as measured by PCR on days 3, 7, 10, 14, 21. A baseline fecal and oropharyngeal sample will be obtained on Day 1 prior to starting dosing of Niclosamide/ placebo.

DRUG

Placebo

The collection of oropharyngeal samples will be observed by a Study Team member via the telehealth platform.

OTHER

Telehealth monitoring

In addition to Niclosamide or placebo treatments, all enrolled patients will be provided a home thermometer as well as a fingertip probe pulse oximeter, with the specific instructions to monitor both temperature at oxygen saturation at the time of daily oral administration of drug. The collection of oropharyngeal samples will be directly observed by a Study Team member via the telehealth platform.

Trial Locations (1)

02111

Tufts Medical Center, Boston

All Listed Sponsors
lead

Tufts Medical Center

OTHER

NCT04399356 - Niclosamide for Mild to Moderate COVID-19 | Biotech Hunter | Biotech Hunter