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Clinical Trial Summary

Safety and immunogenicity one-month study in healthy individuals administered once-daily pill of therapeutic vaccine made from heat-inactivated plasma from donors with COVID-19. Healthy, at least 20, volunteers will be monitored for signs of adverse events. Their PBMC will be collected at baseline and one month later to analyze which type of immune response vaccine has induced.


Clinical Trial Description

Experimental batch of tableted thermostable vaccine obtained from pooled plasma of COVID-19 patients is produced. The goal of this trial is test safety and immunogenicity of once-per-day day administered orally to volunteers for 15 days. Baseline and post-treatment standard safety parameters will be compared. Blood samples from volunteers will be monitored and immunogenicity lab assays will be undertaken to characterize immune response. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04380532
Study type Interventional
Source Immunitor LLC
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date May 15, 2020
Completion date June 15, 2021

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