Clinical Trials Directory

Trials / Unknown

UnknownNCT04421391

QuadraMune(TM) for Prevention of COVID-19

Phase II Study of QuadraMune(TM) for Prevention of COVID-19 in High Risk Populations

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
500 (estimated)
Sponsor
Therapeutic Solutions International · Industry
Sex
All
Age
18 Years – 120 Years
Healthy volunteers
Accepted

Summary

QuadraMune(TM) is a nutritional supplement which has previously been demonstrated to possess antiinflammatory and immune modulatory activity based on in vitro and pilot in vivo studies. The current clinical trial aims to assess in a 500 volunteer trial the efficacy of QuadraMune(TM) in reducing infection in individuals at high risk of COVID-19.

Detailed description

QuadraMune(TM) is composed of 4 natural ingredients. Pterostilbene is an analogue of resveratrol, and has been shown to possess antiinflammatory activity. Additionally, this compound suppresses macrophage activation while enhancing NK activity. Epigallocatechin gallate (EGCG) is one of the active ingredients in green tea and has been shown to act as an activator of T cells, and a suppressor of neutrophil mediated inflammation. Sulforaphane is derived from broccoli and studies have shown that it protects lungs from inflammatory pathology. Thymoquinone, which is chemically related to hydroxychloroquine, possessing antiviral effects and increases NK activity. QuadraMune is a combination of these ingredients and is believed to possess superior in vitro and in vivo therapeutic properties as compared to when the ingredients are administered individually. The study aims to assess preventative effects of QuadraMune(TM) administration for 12 weeks.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTQuadraMune(TM)QuadraMune(TM) is a commercially available nutritional supplement

Timeline

Start date
2020-06-08
Primary completion
2020-11-01
Completion
2020-11-08
First posted
2020-06-09
Last updated
2020-06-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04421391. Inclusion in this directory is not an endorsement.