drugset / Trial / NCT05736835

A Phase 2 Trial of the Immunogenicity and Safety of CVXGA Intranasal COVID Vaccine in Healthy Adults

NCT05736835 ↗

Phase 2 Completed 227 enrolled CyanVac LLC
RandomizedSingle-groupQuadruple-blindTreatment

Summary

The purpose of this trial is to evaluate immunogenicity and safety of CVXGA administered as a single intranasal dose against SARS-CoV-2 S-protein in participants. The trial will enroll up to 400 healthy participants, age 18-80 years.

Timeline

Start
2023-09-21
Primary completion
2025-12-16
Completion
2025-12-16

Drugs

EvaluationDrugModalityDoseRoute
Subject CVXGA Vaccine 1e+07 unknown Intranasal

Indications