Immunogenicity and Safety of an Inactivated COVID-19 Vaccine in Elderly People With Chronic Bronchitis and COPD
Study Details
Study Description
Brief Summary
Evaluation of immunogenicity and safety of the subjects aged 60 years and above with chronic bronchitis and chronic obstructive pulmonary disease recruited to receive the schedule of two doses inactivated COVID-19 vaccine with the interval of 21 days .
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Detailed Description
The subjects aged 60 years and above with chronic bronchitis and chronic obstructive pulmonary disease were recruited to receive the schedule of two doses inactivated COVID-19 vaccine with the interval of 21 days .
Blood samples will be collected 2 times: before the 1st dose of vaccinatioin and 28 days after the 2nd dose of vaccination.
Any local or systemic adverse events that occurred within 21 days after vaccination will be recorded.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Experimental Group A total 400 subjects receive two doses inactivated COVID-19 vaccine with the interval of 21 days |
Biological: Inactivated COVID-19 vaccine
receive two doses inactivated COVID-19 vaccine with the interval of 21 days
|
Outcome Measures
Primary Outcome Measures
- Seroconversion rate [28 days after the 2th dose (Day 49)]
The rate of seroconversion against coronavirus
- Baseline neutralizing antibody level [Before vaccination (Day 0)]
Neutralizing antibody geometric mean titer(GMT) against coronavirus before vaccination
- Neutralizing antibody level [28 days after the 2th dose (Day 49)]
Neutralizing antibody GMT against coronavirus after the 2th dose
Secondary Outcome Measures
- Adverse events rate [0-21days following vaccinations]
Analyse the incidence of adverse events following vaccination, both solicited and unsolicited
- Serious adverse event rate [0-6 months]
Report and analyse serious adverse events
Eligibility Criteria
Criteria
Inclusion criteria:
-
Subjects aged 60 and above with full capacity for civil conduct;
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Chronic bronchitis (or chronic obstructive pulmonary disease) diagnosed by a medical institution at level I or above;
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Body temperature < 37.3 ° C confirmed by clinical examination before enrollment ;
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Able and willing to complete the entire study plan during the study follow-up period;
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Have the ability to understand the study procedures, voluntarily sign informed consent, and comply with the requirements of the clinical study protocol
Exclusion criteria for the first dose:
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Subjects were previously confirmed cases of COVID-19 or asymptomatic infected persons;
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Subjects have history of vaccination against COVID-19;
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Being allergic to any component of vaccines (including excipients) ;
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Injection of non-specific immunoglobulin within 1 month before enrollment;
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Injection of live attenuated vaccines within 1 month and injection of other vaccines within 14 days before enrollment;
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Subjects who have experienced severe allergic reactions to vaccines (e.g. acute anaphylaxis, urticaria, angioneurotic edema, dyspnea, etc.);
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Having uncontrolled epilepsy and other progressive neurological disorders and a history of Guillain-Barre syndrome;
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Having severe liver and kidney diseases, malignant tumors, acute diseases or acute episodes of chronic diseases;
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Have been diagnosed with congenital or acquired immunodeficiency, HIV infection, lymphoma, leukaemia or other autoimmune diseases;
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Have been diagnosed with thrombocytopenia or other clotting disorders that may contraindicate subcutaneous injection;
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During an acute episode of chronic bronchitis/chronic obstructive pulmonary disease;
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Other subjects whose physical conditions, as determined by the investigator, are not suitable for inclusion in clinical studies.
Exclusion criteria for the second dose:
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Subjects who had vaccine-related adverse reactions after the first dose;
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Having high fever (axillary temperature ≥39.0℃) for three days after the first dose of inoculation, or severe allergic reaction;
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Having any adverse nervous system reaction after the first dose;
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During the acute onset of a chronic disease, or the recovery of acute complications less than two weeks;
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Other reasons for exclusion considered by the investigator.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Zhejiang provincial center for disease control and prevention | Hangzhou | Zhejiang | China | 310051 |
Sponsors and Collaborators
- China National Biotec Group Company Limited
- Zhejiang Provincial Center for Disease Control and Prevention
- Beijing Institute of Biological Products Co Ltd.
Investigators
- Principal Investigator: Hanqing He, Zhejiang Provincial Center for Disease Control and Prevention
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- BIBP2021COPD