Clinical Trials Directory

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UnknownNCT04643561

Using Travelan to Boost Immune Response in Vitro to COVID-19

A Feasibility Trial Using Trevalan in Healthy Volunteers for Increasing an in Vitro Immune Response to COVID-19 Proteins

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
5 (estimated)
Sponsor
Hadassah Medical Organization · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Accepted

Summary

The gut immune system was shown as an effective target for inducing systemic immune signals against viruses. Oral administration of Travelan, an over the counter product which contains hyperimmune bovine colostrum was shown in preclinical studies to augment the anti-viral immune towards several strains of influenza viruses (RNA viruses). This study will evaluate the option that Trevalan may help improve the immune system reaction when introduced to COVID-19 proteins in-vitro. 5 healthy volunteers will receive a treatment regimen of 5 days with Trevalan. Before and after treatment, blood samples will be taken in order to test immune response towards viral proteins of the COVID-19 virus in vitro by measuring the number of T cell clone secreting IFNγ against viral antigens.

Conditions

Interventions

TypeNameDescription
OTHERTravelan OTC5 days of treatment with Travelan food supplement 3 times a day, blood will be drawn prior and after intervention

Timeline

Start date
2020-11-01
Primary completion
2020-12-31
Completion
2020-12-31
First posted
2020-11-25
Last updated
2020-11-27

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT04643561. Inclusion in this directory is not an endorsement.