drugset / Trial / NCT04683484

A Clinical Trial to Assess the Safety and Immunogenicity of Nanocovax in Heathy Volunteers

NCT04683484 ↗

RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to assess the safety, tolerability, and immunization of Nanocovax in healthy volunteers.

Timeline

Start
2020-12-10
Primary completion
2021-06-10
Completion
2021-08-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Nanocovax Vaccine 25 ug Intramuscular
Subject Nanocovax Vaccine 50 ug Intramuscular
Subject Nanocovax Vaccine 75 ug Intramuscular

Indications