Not yet recruitingPhase 2NCT07168018
Safety and Immunogenicity of Coadministration of the Candidate Rabies Vaccine ChAdOx2 RabG and Licensed Vaccine
Studying Rabies
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 Oxford
- Principal Investigator
- Alexander D DouglasJenner Institute, University of Oxford
- Intervention
- Coadministration of ChAdOx2 RabG and licensed inactivated rabies vaccine (IRV)(biological)
- Enrollment
- 40 target
- Eligibility
- 18-45 years · All sexes
- Timeline
- 2025 – 2026
Study locations (1)
- Ifakara Health Institute, Bagamoyo, Tanzania
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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