Clinical Trials Directory

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UnknownNCT05105295

Immunogenicity and Safety of a Third Dose and Immune Persistence of BBIBP-Corv Vaccine in People With HIV Infected

Immunogenicity and Safety of a Third Dose and Immune Persistence of BBIBP-Corv Vaccine in People With Human Immunodeficiency Virus Infected

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
400 (estimated)
Sponsor
China National Biotec Group Company Limited · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Evaluation of immunogenicity, safety and persistence of the subjects with HIV infected received the third dose of inactivated COVID-19 vaccine .

Detailed description

The subjects aged ≥18 years with HIV infected who have completed the schedule of two doses for 3 months recruited to receive a third dose of inactivated COVID-19 vaccine. Blood samples will be collected 3 times: before the third dose of vaccinatioin,28 days and 6 months after the third dose of vaccination. Any local or systemic adverse events that occurred within 21 days after vaccination will be recorded.

Conditions

Interventions

TypeNameDescription
BIOLOGICALInactivated COVID-19 vaccinereceive a third dose of inactivated COVID-19 vaccine

Timeline

Start date
2021-12-01
Primary completion
2022-06-30
Completion
2022-06-30
First posted
2021-11-03
Last updated
2021-11-03

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05105295. Inclusion in this directory is not an endorsement.