CompletedPhase 1NCT05272605
Safety and Immune Response of Adjuvanted SARS-CoV-2 (COVID-19) Beta Variant RBD Recombinant Protein (DoCo-Pro-RBD-1 + MF59®) and mRNA (MIPSCo-mRNA-RBD-1) Vaccines in Healthy Adults
Studying Severe acute respiratory syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University of Melbourne
- Principal Investigator
- Prof. Terry Nolan, M.DPeter Doherty Institute for Infection and Immunity, The University of Melbourne
- Intervention
- Adjuvanted SARS-CoV-2 beta variant RBD recombinant protein vaccine (DoCo-Pro-RBD-1 + MF59)(biological)
- Enrollment
- 76 target
- Eligibility
- 18-64 years · All sexes
- Timeline
- 2022 – 2023
Study locations (2)
- Vaccine and Immunisation Research Group, Doherty Institute, University of Melbourne, Melbourne, Victoria, Australia
- Royal Melbourne Hospital, Victorian Infectious Diseases Service (VIDS), Melbourne, Victoria, Australia
Collaborators
Southern Star Research
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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