Immunogenicity and Safety of 23-valent Pneumococcal Polysaccharide Vaccine
- Conditions
- Pneumococcal Infections
- Interventions
- Biological: Experimental 23-valent PPVBiological: Control 23-valent PPV
- Registration Number
- NCT05477693
- Lead Sponsor
- Sinovac Biotech Co., Ltd
- Brief Summary
This is a randomized, double-blind, positive-controlled phase Ⅳ clinical trial of 23-valent pneumococcal polysaccharide vaccine manufactured by Sinovac Biotech Co., Ltd.The purpose of this study is to evaluate the immunogenicity and safety of 23-valent pneumococcal polysaccharide vaccine in population aged 2 years and older.
- Detailed Description
This study is a randomized, double-blind, positive-controlled phase Ⅳ clinical trial to evaluate the immunogenicity and safety of 23-valent pneumococcal polysaccharide vaccine in population aged 2 years and older.The experimental vaccine was manufactured by Sinovac Biotech Co., Ltd,the control vaccine was manufactured by Merck Sharp \& Dohme.A total of 1800 subjects including 900 subjects aged 2\~17 years,360 subjects aged 18\~59 years and 540 subjects aged 60 years and above will be enrolled.Subjects in each age group will be randomly divided into two groups according to the ratio of 2:1, and received one dose of experimental vaccine or control vaccine.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 1800
- Children aged 2 years and above in stable health;
- The subjects and/or guardians can understand and voluntarily sign the informed consent form (For subjects aged 8-17 years, both subjects and guardians need to sign the informed consent form.If the subject aged 16 to 17 years with full capacity for civil conduct and his/her labor income is his/her main source of living, the informed consent can be signed only by the subject himself/herself);
- Proven legal identity.
- Have received any pneumococcal vaccine;
- History bacterial pneumonia or invasive pneumococcal infectious diseases caused by pneumococci and confirmed by culture.
- Women of childbearing age (menarche to premenopause) are pregnant (including positive urine pregnancy test), breastfeeding or planning pregnancy within 1 month;
- History of asthma, allergy to vaccines or vaccine components, and serious adverse reactions to vaccines, such as urticaria, dyspnea, and angioneurotic edema;
- Severe chronic diseases,such as severe cardiovascular diseases, hypertension(Systolic blood pressure ≥140mmHg and/or diastolic blood pressure ≥90mmHg) and diabetes that cannot be controlled by drugs, liver or kidney diseases,malignant tumors, etc.;
- Severe neurological disease (epilepsy, convulsions or convulsions) or mental illness;
- Diagnosed abnormal blood coagulation function (eg, lack of blood coagulation factors, blood coagulopathy, abnormal platelets) or obvious bruising or blood coagulation;
- Immunosuppressive therapy, cytotoxic therapy, inhaled corticosteroids (excluding allergic rhinitis corticosteroid spray therapy, acute noncomplicated dermatitis superficial corticosteroid therapy) in the past 6 months;
- A long history of alcohol or drug abuse;
- Receipt of blood products within in the past 3 months;
- Receipt of other investigational drugs within 30 days prior to receiving the investigational vaccine;
- Receipt of attenuated live vaccines or COVID-19 vaccines in the past 14 days;
- Receipt of inactivated or subunit vaccines in the past 7 days;
- Onset of various acute or chronic diseases within 3 days prior to the study;
- Underarm body temperature before vaccination>37.0°C;
- The subjects participated in other clinical trials during the follow-up period or will be planned to participate other clinical trials within 1 months;
- According to the investigator's judgment, the subject has any other factors that are not suitable for participating in the clinical trial.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Experimental Group Experimental 23-valent PPV 1200 participants(including 600 subjects aged 2\~17 years,240 subjects aged 18\~59 years and 360 subjects aged 60 years and above)received one dose of 23-valent pneumococcal polysaccharide vaccine manufactured by Sinovac Biotech Co., Ltd Control Group Control 23-valent PPV 600 participants(including 300 subjects aged 2\~17 years,120 subjects aged 18\~59 years and 180 subjects aged 60 years and above)received one dose of 23-valent pneumococcal polysaccharide vaccine manufactured by Merck Sharp \& Dohme.
- Primary Outcome Measures
Name Time Method Immunogenicity index-Seroconversion rate (2-fold increase rate) 30 days after vaccination Seroconversion rate (2-fold increase rate)for serotype specificity (3, 6B, 14, 19A, 19F, 23F) of pneumococcal immunoglobulin G (IgG) antibody 30 days after vaccination.
- Secondary Outcome Measures
Name Time Method Immunogenicity index-Seroconversion rate 30 days after vaccination Seroconversion rate for serotype specificity （1、2、4、5、7F、8、9N、9V、10A、11A、12F、15B、17F、18C、20、22F and 33F）of pneumococcal IgG antibody 30 days after vaccination.
Immunogenicity index-GMC 30 days after vaccination Geometric Mean Concentration (GMC) for serotype specificity （1、2、4、5、7F、8、9N、9V、10A、11A、12F、15B、17F、18C、20、22F and 33F）of pneumococcal IgG antibody 30 days after vaccination.
Immunogenicity index-GMI 30 days after vaccination Geometric Mean Increase (GMI) for serotype specificity （1、2、4、5、7F、8、9N、9V、10A、11A、12F、15B、17F、18C、20、22F and 33F）of pneumococcal IgG antibody 30 days after vaccination.
Immunogenicity index-Geometric Mean Concentration (GMC) 30 days after vaccination Geometric Mean Concentration (GMC) for serotype specificity (3, 6B, 14, 19A, 19F, 23F) of pneumococcal IgG antibody 30 days after vaccination.
Immunogenicity index-Geometric Mean Increase (GMI) 30 days after vaccination Geometric Mean Increase (GMI) for serotype specificity (3, 6B, 14, 19A, 19F, 23F) of pneumococcal IgG antibody 30 days after vaccination.
Safety index-Incidence of adverse reactions Within 30 days after vaccination Incidence of adverse reactions within 30 days after vaccination.
Safety index-incidence of adverse reactions Within 7 days after vaccination Incidence of adverse reactions within 7 days after vaccination
Safety index-Incidence of serious adverse events Within 30 days after vaccination Incidence of serious adverse events within 30 days after vaccination.
Trial Locations
- Locations (1)
Linwei District Center for Disease Control and Prevention
🇨🇳Weinan, Shanxi, China