Safety, tolerability, immunogenicity, and plasmapheresis-based antibody collection in a phase 1b open label trial of two investigational monovalent chimpanzee adenoviral vectored filovirus vaccines, cAd3-Sudan and cAd3-Marburg, in healthy adults
Year: 2025
Type: article
Study design: Clinical Trial
Abstract: BACKGROUND: Sudan virus and Marburg virus are high priority biological threat pathogens with fatality rates of 25-90%. Recent outbreaks in Uganda, Equatorial Guinea, and Rwanda between 2022 and 2025 emphasise the critical need for effective vaccines. The aim of this phase 1b study was to determine clinical safety, tolerability, and immunogenicity of these monovalent vaccines. Plasmapheresis was used to collect hyper-immune plasma for use in future assay standardisation. METHODS: particle units/dose and were followed up for 181 ± 14 days. The trial was single arm with respect to each vaccine. Primary safety and tolerability endpoints were assessed in all subjects by reactogenicity for initial 7 days, adverse events for the first 28 days, and serious adverse events (SAEs) throughout the study. Secondary immunogenicity endpoints included evaluation of binding antibodies against the viral glycoproteins as measured by ELISA. FINDINGS: Thirty-two healthy adults were enrolled in the trial; the most commonly reported signs within 7 days of vaccination were mild headache and mild or moderate myalgia. No SAEs or deaths were reported. Binding antibodies (IgG) persisted at 9 weeks in all subjects in both groups; time to seroconversion was 14 days in both groups; peak IgG response across study participants was achieved by Day 29. INTERPRETATION: These vaccines are safe, immunogenic and rapidly induced glycoprotein-specific antibody responses in all participants. FUNDING: Funding was provided by the Biomedical Advanced Research and Development Authority (BARDA), USA, under contract 75A50119C00055.
Source: EBioMedicine
Authors: Ekaterina Vert-Wong, Michael E. Stevenson, Roxana Rustomjee, Courtney L. Finch, Jocelyn Jakubik, Thomas H. King
Institutions: Sabin Vaccine Institute, Oklahoma Blood Institute
Language: English
Subfield: Infectious Diseases
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $5,780
Funders: Administration for Strategic Preparedness and Response, U.S. Department of Health and Human Services, Sabin Vaccine Institute, Vaccine Research Center, National Institutes of Health, Biomedical Advanced Research and Development Authority, National Institute of Allergy and Infectious Diseases
Award: G4503118948
OpenAlex ID: W4413963012
