Safety and Immunogenicity of an Inactivated West Nile Virus Vaccine in Healthy Adults

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

February 24, 2025

Primary Completion Date

October 1, 2026

Study Completion Date

November 1, 2027

Conditions
West Nile Viral Infection
Interventions
BIOLOGICAL

HydroVax-001B WNV

A vaccine to West Nile Virus (WNV) that is prepared by propagating naturally attenuated Kunjin strain of WNV on well characterized low-passage Vero cells. The vaccine contains 10 mcg of inactivated purified whole virion WNV formulated in a volume of 0.5 mL/dose with 0.10% aluminum hydroxide, 10% D-sorbitol, 0.001% Polysorbate 80 (Tween80) in 10 mM phosphate-buffer with 350 mM NaCl.

OTHER

Placebo

Placebo

OTHER

Sodium Chloride, 0.9%

0.9% Sodium Chloride Injection

Trial Locations (1)

63104-1015

Saint Louis University Center for Vaccine Development, St Louis

All Listed Sponsors
lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

NCT06745921 - Safety and Immunogenicity of an Inactivated West Nile Virus Vaccine in Healthy Adults | Biotech Hunter | Biotech Hunter