Clinical Trials Directory

Trials / Unknown

UnknownNCT05552950

The Efficacy and Safety of BioBlock® Intranasally Administered Virus-Neutralizing Bovine Colostrum Nasal Spray in Preventing of COVID-19 (Coronavirus Disease-19) Infection in Healthy Volunteer Individuals

Randomized, Controlled, Double-Blind Proof of Concept Trial Assessing the Efficacy and Safety of BioBlock® Intranasally Administered Virus-Neutralizing Bovine Colostrum Nasal Spray in Preventing of COVID-19 Infection in Healthy Volunteer Individuals

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
2,000 (estimated)
Sponsor
Chemi-Pharm AS · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

This is a proof-of-concept double-blind cluster randomized (1:1) parallel study. The randomization unit is healthy volunteers who have no symptoms of COVID-19 at the start of the study and have not been infected with the SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) virus in the past 90 days. The selected individuals are randomly grouped in either the experimental group (individuals using the BioBlock® antiviral nasal spray immediately after waking up in the morning and thereafter once every 4 hours and so for 28 days) or the control group (placebo is used by individuals immediately after waking up in the morning and thereafter once every 4 hours and so for 28 days).

Conditions

Interventions

TypeNameDescription
BIOLOGICALBioBlock® antiviral nasal spraySARS-CoV-2 BioBlock is a natural preparation derived from bovine colostrum, where animals have an immune response against the SARS-CoV-2 spike protein in addition to conventional vaccines. The antiviral colostrum preparation was made from colostrum of cows immunized with SARS CoV-2 spike protein. Pregnant cows were immunized during the third trimester of gestation using a non-infectious recombinantly produced and purified SARS CoV-2 spike protein. Colostrum, which is milked after calving, concentrates most of the antibodies produced in the cow's body at very high concentrations, including neutralizing antibodies to SARS CoV-2 produced as a result of immunization.

Timeline

Start date
2022-05-01
Primary completion
2023-07-31
Completion
2023-12-30
First posted
2022-09-23
Last updated
2023-02-08

Locations

1 site across 1 country: Estonia

Source: ClinicalTrials.gov record NCT05552950. Inclusion in this directory is not an endorsement.