Evaluation of the Immunogenicity and Safety BBIBP-CorV Vaccine for COVID-19 in Adults in Guinea
NCT05409300 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 200
Last updated 2024-03-27
Summary
Phase II, non-randomized, open-label, comparative, single center national trial in Guinea, aimed to assess the humoral vaccine immune response induced by BBIBP-CorV vaccine in 200 adults aged between 18 and 45 years or 55 or older, one month after receiving the complete COVID-19 vaccination schedule.
Conditions
- COVID-19
- Vaccine Adverse Reaction
- Sars-CoV-2 Infection
- Healthy Volunteer
Interventions
- BIOLOGICAL
-
BBIBP-CorV
Inactivated COVID19 vaccine, adjuvanted with aluminum hydroxide
Sponsors & Collaborators
-
CEPI
collaborator OTHER -
Alliance for International Medical Action
collaborator OTHER -
Centre National de Formation et de Recherche en Sante Rurale
collaborator OTHER_GOV -
Institut National de la Santé Et de la Recherche Médicale, France
collaborator OTHER_GOV -
APHP
collaborator OTHER -
Agence Nationale de Sécurité Sanitaire de la Guinée (ANSS Guinée)
collaborator UNKNOWN -
Innovative clinical research network in vaccinology (IREIVAC)
collaborator UNKNOWN -
ANRS, Emerging Infectious Diseases
lead OTHER_GOV
Principal Investigators
-
Odile Launay · Innovative clinical research network in vaccinology (I-REIVAC)
-
Abdoul Habib Beavogui · Centre National de Formation et de Recherche en Santé Rurale (CNFRSR)
Study Design
- Allocation
- NA
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-04-25
- Primary Completion
- 2023-08-03
- Completion
- 2025-02-28
Countries
- Guinea
Study Locations
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