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NCT05493917

A Real-world Study to Evaluate the Safety and Immunogenicity of a Third-dose Booster After Two Doses of an Inactivated COVID-19 Vaccine

Status unknown Last updated 9 August 2022
What this trial tests

trial testing an inactivated SARS-CoV-2 vaccine named BBIBP-CorV in COVID-19 in 2,000 participants. Status unknown.

Timeline
3 November 2021
Primary endpoint
31 December 2022
31 December 2022

Quick facts

Lead sponsorHuashan Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment2,000
Start date3 November 2021
Primary completion31 December 2022
Estimated completion31 December 2022
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Huashan Hospital

Who can join

18 and older, any sex, with COVID-19 or Vaccine Reaction. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This project is a prospective observational real-world study, recruiting and screening subjects who have completed 2 doses of the COVID-19 vaccine for more than 6 months and receive the third dose of the vaccine voluntarily into the clinical cohort of this study. Subjects received a third dose of the COVID-19 vaccine will be enrolled in the study and followed up for 1 year at baseline (day 0) before vaccine injection, 28 days after injection, 90 days, 270 days after injection. On the 365th day, blood samples were collected for the detection of anti-SARS-CoV-2 antibodies and other related indicators to evaluate the immune protection effect.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for COVID-19

Currently open trials in the same condition.

Other Huashan Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05493917.

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