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GLS-5310 Vaccine in Healthy Volunteers as a Booster for SARS-CoV-2 (COVID-19)

Healthy Clinical Trial

Official title:
Safety, Tolerability and Immunogenicity of GLS-5310 DNA Vaccine Given as a Booster to Those Previously Vaccinated Against SARS-CoV-2

Clinical Trial Summary

Phase I study to assess the safety, tolerability and immunogenicity of GLS-5310 DNA vaccine given as a booster to those previously vaccinated against SARS-CoV-2

Clinical Trial Description

This Phase I, randomized, placebo-controlled study will assess the safety, tolerability, and immunogenicity of GLS-5310 DNA vaccine administered intradermally (ID) with or without concomitant intranasal (IN) administration given as a heterologous booster dose to those previously vaccinated against SARS-CoV-2. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05182567
Study type Interventional
Source GeneOne Life Science, Inc.
Contact
Status Active, not recruiting
Phase Phase 1
Start date May 23, 2022
Completion date December 2023
View Details
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