Safety and Immunogenicity of the Candidate Rabies Vaccine ChAdOx2 RabG
NCT04162600 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 18
Last updated 2024-11-08
Summary
This is a first-in-human, open-label, dose escalation, phase I clinical trial to assess the safety and immunogenicity of the candidate ChAdOx2 RabG vaccine in healthy UK volunteers aged 18-65. The vaccine will be administered intramuscularly (IM).
Conditions
- Rabies
Interventions
- BIOLOGICAL
-
ChAdOx2 RabG
Single dose of ChAdOx2 RabG at different concentrations: 5 x 10\^9 vp, 2.5 x 10\^10 vp, 5 x 10\^10 vp
- BIOLOGICAL
-
Inactivated Rabies Vaccine
A complete pre-exposure prophylactic course of an existing rabies vaccine, ≥2.5 international units.
- BIOLOGICAL
-
ChAdOx2 RabG
Single dose of ChAdOx2 RabG at different concentrations: 5 x 10\^9 vp, 2.5 x 10\^10 vp, 5 x 10\^10 vp
- BIOLOGICAL
-
ChAdOx2 RabG
Single dose of ChAdOx2 RabG at different concentrations: 5 x 10\^9 vp, 2.5 x 10\^10 vp, 5 x 10\^10 vp.
- BIOLOGICAL
-
Inactivated Rabies Vaccine
A complete pre-exposure prophylactic course of an existing rabies vaccine, ≥2.5 international units.
- BIOLOGICAL
-
Inactivated Rabies Vaccine
A complete pre-exposure prophylactic course of an existing rabies vaccine, ≥2.5 international units.
Sponsors & Collaborators
-
University of Oxford
lead OTHER
Principal Investigators
-
Alexander D Douglas · Jenner Institute
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-01-02
- Primary Completion
- 2024-07-10
- Completion
- 2024-07-10
Countries
- United Kingdom
Study Locations
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