A Phase 1/2 Study to Determine Safety and Immunogenicity of Two COVID 19 Vaccines VB10.2129 (RBD Candidate) and VB10.2210 (T Cell Candidate) Previously Vaccinated in Healthy Adult Volunteers

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

68

Participants

Timeline

Start Date

November 1, 2021

Primary Completion Date

December 16, 2022

Study Completion Date

May 30, 2023

Conditions
COVID-19Infection ViralInfections
Interventions
BIOLOGICAL

VB10.2129

0.3 mg, 1 mg or 3 mg on Day 0 and Day 21 or 3 mg on Day 0

BIOLOGICAL

VB10.2210

3 doses (dose to be determined) on Day 0 and Day 21 or highest dose (TBD) on Day 0

Trial Locations (2)

5020

Haukeland University Hospital, Klinisk Forskningspost, Bergen

Unknown

Oslo University Hospital Ullevål Sykehus, Dept. Infection Diseases, Oslo

Sponsors
All Listed Sponsors
collaborator

Vaccibody AS

INDUSTRY

lead

Nykode Therapeutics ASA

INDUSTRY