Covid19, SARS-CoV-2 Infection
Conditions
Keywords
SARS-CoV-2, Covid19, Inactivated vaccine
Brief summary
With the unprecedented morbidity of the COVID-19 pandemic, the vaccine effectiveness needs to be assessed across diverse populations. The purpose of this study is to evaluate the safety and immunogenicity of an inactivated SARS-CoV-2 vaccine in medical workers.
Detailed description
1370 participants who were negative for serum-specific antibodies against SARS-CoV-2 at the time of screening were enrolled and were receive a two-dose schedule, 21 days apart, with 4 μg BBIBP-CorV inactivated SARS-CoV-2 vaccine. The primary safety outcome includes solicited local and systemic reactions prompted by and recorded in an electronic diary within 7 days post each injection, unsolicited adverse events and serious adverse events assessed from the receipt of each dose, and clinical laboratory abnormalities from dose 1 through 1month after dose 2. Laboratory tests included measurement of alanine aminotransferase, aspartate aminotransferase, serum total bilirubin, serum albumin, creatinine, blood urea nitrogen, and blood routine examination. Immunogenicity was assessed as the serum anti-SARS-CoV-2 specific antibody responses and neutralizing activity at 4 weeks after the second vaccination.
Interventions
The subjects of Vaccination Group will receive two doses, 21 days apart of inactivated SARS-CoV-2 vaccine (4 μg of BBIBP-CorV)
Sponsors
Study design
Eligibility
Inclusion criteria
* Written informed consent according to ICH/GCP regulations prior to any trial specific procedures. * Male or female aged 18-59 years.
Exclusion criteria
* NA
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of participants reporting local reactions | within 7days post each vaccination | Pain at the injection site, swelling, itch, and redness |
| Percentage of participants reporting systemic events | within 7days post each vaccination | Fever, headache, fatigue, nausea, vomiting, diarrhea, constipation, myalgia, arthralgia |
| Percentage of participants reporting adverse events | From Dose 1 through 1 month after Dose 2 | verified by investigators |
| Percentage of participants reporting serious adverse events | From Dose 1 through 1 month after Dose 2 | verified by investigators |
| Serum anti-SARS-CoV-2 speicfic antibody and neutralizing antibody titres | at 1 month after dose 2 | determination of anti-SARS-CoV-2 speicfic antibody and SARS-CoV-2 neutralizing antibody levels |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Serum anti-SARS-CoV-2 speicfic antibody and neutralizing antibody titres | at 6 months after dose 2 | determination of anti-SARS-CoV-2 speicfic antibody and SARS-CoV-2 neutralizing antibody levels |
Countries
China