Immunogenicity and Safety of ChulaCov19 BNA159 and ChulaCov19 BNA159.2 Vaccines as a Booster Dose in Adults

PHASE2CompletedINTERVENTIONAL
Enrollment

150

Participants

Timeline

Start Date

January 19, 2023

Primary Completion Date

July 15, 2024

Study Completion Date

November 18, 2024

Conditions
COVID-19, SARS CoV 2 Infection
Interventions
BIOLOGICAL

ChulaCov19 BNA159 vaccine (50 mcg)

Single dose of ChulaCov19 BNA159 vaccine 0.5 ml will be given by IM at Day 1

BIOLOGICAL

Pfizer/BNT vaccine (30 mcg)

Single dose of Pfizer/BNT vaccine 0.3 ml will be given by IM at Day 1

BIOLOGICAL

COMVIGEN (ChulaCov19 BNA159.2) vaccine (50 mcg)

Single dose of COMVIGEN vaccine 0.5 ml will be given by IM at Day 1

Trial Locations (5)

2145

The Children's Hospital at Westmead Sydney, Westmead

2148

Paratus Clinical Research Western Sydney, Blacktown

2259

Paratus Clinical Research Central Coast, Kanwal

2617

Paratus research Canberra Clinic, Bruce

4010

Paratus Clinical Research- Brisbane Clinic, Albion

Sponsors
All Listed Sponsors
collaborator

Chulalongkorn University

OTHER

collaborator

BioNet-Asia

UNKNOWN

collaborator

Southern Star Research

INDUSTRY

lead

Technovalia, Pty Ltd

INDUSTRY

NCT05605470 - Immunogenicity and Safety of ChulaCov19 BNA159 and ChulaCov19 BNA159.2 Vaccines as a Booster Dose in Adults | Biotech Hunter | Biotech Hunter