Phase 1 Study to Evaluate the Safety and Immunogenicity of a Candidate Vaccine Against Respiratory Syncytial Virus

PHASE1CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

September 7, 2020

Primary Completion Date

March 2, 2022

Study Completion Date

March 2, 2022

Conditions
Acute Bronchiolitis Due to Respiratory Syncytial Virus
Interventions
BIOLOGICAL

V-306 candidate vaccine

"Each V-306 monomer consists of the following elements:~1. A Lipopeptide Building Block that contains an optimized, artificially designed coiled-coil domain, which self-assembles into highly stable trimers.~2. A 'universal' T-helper epitope fused at the C-terminus of the coiled-coil domain.~3. A lipid component di-palmitoyl-S-glyceryl cysteine (Pam2C), fused at the N-terminus.~4. A mimetic of the Palivizumab epitope, referred to RSV F-protein site II antigen mimetic (FsIIm), which is coupled near the C-terminus of the Lipopeptide Building Block via a short maleimide-PEG-oxime linker."

Trial Locations (1)

9000

Centre for Vaccinology (CEVAC), Ghent

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Center of Vaccinology, Ghent, Belgium (CEVAC)

UNKNOWN

collaborator

Expert Clinical Services Organization, Brussels, Belgium (ECSOR)

UNKNOWN

lead

Virometix

INDUSTRY

NCT04519073 - Phase 1 Study to Evaluate the Safety and Immunogenicity of a Candidate Vaccine Against Respiratory Syncytial Virus | Biotech Hunter | Biotech Hunter