Pneumococcal 13-valent Conjugate Vaccine
Conditions
Keywords
vaccine, safety
Brief summary
This study evaluates the safety of Pneumococcal 13-valent Conjugate Vaccine in Healthy People Aged 2 Months and Older.120 Subjects will be equally divided into 4 groups,including 18 years and older,2-5 years old, 2 months old and 3 months old. Subjects aged 18 years and 2-5 years old will receive one dose of PCV13 vaccine,while subjects aged 2 and 3 months will receive 3 doses of PCV13 vaccine,injected at 2, 4, 6 months or 3、4、5 months respectively.
Interventions
BIOLOGICALOne dose of PCV13a vaccine
BIOLOGICALthree doses of PCV13a vaccine
Sponsors
Beijing Chaoyang District Centre for Disease Control and Prevention
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
2 Months to No maximum
Healthy volunteers
Yes
Inclusion criteria
1. Healthy babies with health conditions confirmed according to medical history, medical examination and judgment of researchers; 2. Satisfy the age requirements of the clinical trial.(children from 2 months to 5 years old and adults over the age of 18); 3. Parents or guardians of the subjects must provide informed consent forms with personally signature and date; 4. Parents or guardians of the subjects have been informed of all aspects of the research; 5. Subjects or guardians can obey the requirements of the clinical research; 6. No pneumococcal vaccine inoculation history, no other preventive vaccination within 7 days; 7. Axillary temperature below 37℃
Exclusion criteria
1. People with pneumococcal vaccine inoculation history, no matter experimentally or already on the market; 2. People has allergic reaction to any drugs, vaccine or vaccine-related components previously; 3. People has allergic reaction to 13vPnC, 7vPnC or other complexes associated with the drug, known or suspected; 4. People has hemorrhagic physical constitution or diseases that prolong bleeding time, intramuscular injection taboo; 5. People has immune deficiency or immune function inhibition, known or suspected; 6. People has irritability, convulsions, epilepsy, brain diseases and mental history or family history; 7. People has culture-confirmed invasive diseases caused by streptococcus pneumoniae history; 8. People has serious congenital malformations or serious chronic diseases that are known, people with congenital deformities, stunted or has a clinical diagnosis of serious chronic diseases (such as Down syndrome, diabetes, sickle cell anemia or nerve disorders, Guillain-Barre syndrome); 9. People suffers from these diseases: respiratory diseases, acute or chronic active stage of infection, severe cardiovascular disease, kidney and liver diseases, malignant tumors, skin diseases, babies with HIV infected mothers(inspection report is available); 10. People with vaccination-related contraindications that other researchers believe; 11. People take part in other clinical trials while taking part in this clinical trial or 28 days before this clinical trial. People who participate in purely observational studies are acceptable; 12. People received blood products or intravenous immunoglobulin. People who was inoculated Hepatitis B immunoglobulin can be acceptable.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Evaluate the rate of adverse reactions of pneumococcal 13-valent conjugate vaccine | 3 months | Adverse reactions associated with vaccine will be observed in subjects after vaccination. Solicited local adverse events include Pain, Redness, Swelling, Induration, Rash, Pruritus at injection site. solicited general adverse events include Fever, Nausea, Vomiting, Diarrhea, Decreased appetite, Be agitated (irritability, abnormal crying), fatigue, allergy |
Outcome results
None listed