Immunogenicity and Safety Study of the 13-valent Pneumococcal Polysaccharide Conjugate Vaccine in 2-71 Months Old Healthy Infants and Toddlers (the Youngest Could be 6 Weeks Old)
Primary Purpose
Diseases Caused by Streptococcus Pneumoniae Serotypes
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
7-valent pneumococcal conjugate vaccine
13-valent pneumococcal polysaccharide conjugate vaccine
Sponsored by
About this trial
This is an interventional prevention trial for Diseases Caused by Streptococcus Pneumoniae Serotypes
Eligibility Criteria
Inclusion Criteria:
- 2-71 months (the youngest could be 6 weeks old) infants or toddlers which are positively healthy based on the medical history, the physical examination and the judgment of the investigator;
- The statutory guardian (or the consignor) of the subject agree his/her child participate in the study, and is willing to sign the informed consent form;
- The subject and his/her statutory guardians (or the consignor) are able to comply with the requests of the clinical study protocol;
- Never be immunized with any pneumococcus vaccine, and didn't get immunization with any other preventive product in the past 10 days (didn't get immunized with attenuated live vaccine in the past 14 days);
- The auxillary temperature ≤37℃.
Exclusion Criteria:
- Has already been immunized with pneumococcus vaccine no matter it is experimental or marketed;
- With the history of invasive disease caused by streptococcus pneumonia by culture;
- With the history of serious allergy to any vaccine or drug, has got fever higher than 39℃ related to immunization with preventive biological product;
- Infant that the birth weight is lighter than 2.5 kg;
- With the history or the family history of seizure, epilepsy, cerebropathy and psychosis ;
- Infant with the abnormal labor (difficult labor, deliver with apparatus) or with the history of asphyxia or nervous damage;
- With the history of thrombocytopenia or other coagulation disorders by definite diagnosis;
- Infant or toddler with pathological jaundice by diagnosis;
- Be known with or suspected with immunological dysfunction, including immunosuppressive therapy (radiotherapy, chemotherapy, corticosteroid hormone, antimetabolites, cytotoxic drug), HIV infection etc. ;
- Be known with serious congenital malformation or serious chronic disease; suffer from congenital malformation or be diagnosed with serious chronic disease (eg. Down syndrome, diabetes mellitus, sickle cell anemia or nervous disease, Guillain-Barre syndrome);
- Be known with or suspected with diseases including: disease of respiratory system, acute infection or the active period of chronic disease, serious cardiovascular disease, hepatic-nephrotic disease, malignant tumor, skin disease;
- Has taken blood product or globulin (the hepatitis B immune globulin is allowed);
- Be participating in other clinical trials;
- Any other situation which is considered to influence the evaluation of the study by investigators .
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Control Arm
Test Arm
Arm Description
7-valent pneumococcal conjugate vaccine
13-valent pneumococcal conjugate vaccine
Outcomes
Primary Outcome Measures
positive rate after infant doses
the rate of the immunoglobulin G ≥0.35μg/ml after infant doses
GMC after infant doses
geometrical mean concentration of immunoglobulin G after infant doses
positive rate after booster dose
the rate of the immunoglobulin G ≥0.35μg/ml after booster dose
GMC after booster dose
geometrical mean concentration of immunoglobulin G after booster dose
Secondary Outcome Measures
Full Information
NCT ID
NCT02736240
First Posted
March 31, 2016
Last Updated
October 11, 2020
Sponsor
Walvax Biotechnology Co., Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT02736240
Brief Title
Immunogenicity and Safety Study of the 13-valent Pneumococcal Polysaccharide Conjugate Vaccine in 2-71 Months Old Healthy Infants and Toddlers (the Youngest Could be 6 Weeks Old)
Official Title
Immunogenicity and Safety Study of the 13-valent Pneumococcal Polysaccharide Conjugate Vaccine Developed Cooperatively by YunNan Walvax Biotechnology Co., Lt and Yuxi Walvax Biotechnology Co., Lt Among 2-71 Months (the Youngest Could be 6 Weeks) Healthy Infants and Toddlers by Randomized Blind Method With Similar Control in Multi-centers.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
April 8, 2016 (Actual)
Primary Completion Date
December 3, 2017 (Actual)
Study Completion Date
December 3, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Walvax Biotechnology Co., Ltd.
4. Oversight
5. Study Description
Brief Summary
The purpose of this study is to investigate and valuate the immunogenicity and safety of the 13-valent pneumococcal polysaccharide conjugate vaccine in 2-71 months old healthy infants and toddlers (the youngest could be 6 weeks old)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diseases Caused by Streptococcus Pneumoniae Serotypes
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
2760 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control Arm
Arm Type
Active Comparator
Arm Description
7-valent pneumococcal conjugate vaccine
Arm Title
Test Arm
Arm Type
Experimental
Arm Description
13-valent pneumococcal conjugate vaccine
Intervention Type
Biological
Intervention Name(s)
7-valent pneumococcal conjugate vaccine
Intervention Type
Biological
Intervention Name(s)
13-valent pneumococcal polysaccharide conjugate vaccine
Primary Outcome Measure Information:
Title
positive rate after infant doses
Description
the rate of the immunoglobulin G ≥0.35μg/ml after infant doses
Time Frame
30 days after infant doses
Title
GMC after infant doses
Description
geometrical mean concentration of immunoglobulin G after infant doses
Time Frame
30 days after infant doses
Title
positive rate after booster dose
Description
the rate of the immunoglobulin G ≥0.35μg/ml after booster dose
Time Frame
30 days after booster dose
Title
GMC after booster dose
Description
geometrical mean concentration of immunoglobulin G after booster dose
Time Frame
30 days after booster dose
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Months
Maximum Age & Unit of Time
71 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
2-71 months (the youngest could be 6 weeks old) infants or toddlers which are positively healthy based on the medical history, the physical examination and the judgment of the investigator;
The statutory guardian (or the consignor) of the subject agree his/her child participate in the study, and is willing to sign the informed consent form;
The subject and his/her statutory guardians (or the consignor) are able to comply with the requests of the clinical study protocol;
Never be immunized with any pneumococcus vaccine, and didn't get immunization with any other preventive product in the past 10 days (didn't get immunized with attenuated live vaccine in the past 14 days);
The auxillary temperature ≤37℃.
Exclusion Criteria:
Has already been immunized with pneumococcus vaccine no matter it is experimental or marketed;
With the history of invasive disease caused by streptococcus pneumonia by culture;
With the history of serious allergy to any vaccine or drug, has got fever higher than 39℃ related to immunization with preventive biological product;
Infant that the birth weight is lighter than 2.5 kg;
With the history or the family history of seizure, epilepsy, cerebropathy and psychosis ;
Infant with the abnormal labor (difficult labor, deliver with apparatus) or with the history of asphyxia or nervous damage;
With the history of thrombocytopenia or other coagulation disorders by definite diagnosis;
Infant or toddler with pathological jaundice by diagnosis;
Be known with or suspected with immunological dysfunction, including immunosuppressive therapy (radiotherapy, chemotherapy, corticosteroid hormone, antimetabolites, cytotoxic drug), HIV infection etc. ;
Be known with serious congenital malformation or serious chronic disease; suffer from congenital malformation or be diagnosed with serious chronic disease (eg. Down syndrome, diabetes mellitus, sickle cell anemia or nervous disease, Guillain-Barre syndrome);
Be known with or suspected with diseases including: disease of respiratory system, acute infection or the active period of chronic disease, serious cardiovascular disease, hepatic-nephrotic disease, malignant tumor, skin disease;
Has taken blood product or globulin (the hepatitis B immune globulin is allowed);
Be participating in other clinical trials;
Any other situation which is considered to influence the evaluation of the study by investigators .
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nianmin Shi
Organizational Affiliation
Beijing Chaoyang disease control and prevention center
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
27798013
Citation
Chen JJ, Yuan L, Huang Z, Shi NM, Zhao YL, Xia SL, Li GH, Li RC, Li YP, Yang SY, Xia JL. Safety and immunogenicity of a new 13-valent pneumococcal conjugate vaccine versus a licensed 7-valent pneumococcal conjugate vaccine: a study protocol of a randomised non-inferiority trial in China. BMJ Open. 2016 Oct 19;6(10):e012488. doi: 10.1136/bmjopen-2016-012488.
Results Reference
derived
Learn more about this trial
Immunogenicity and Safety Study of the 13-valent Pneumococcal Polysaccharide Conjugate Vaccine in 2-71 Months Old Healthy Infants and Toddlers (the Youngest Could be 6 Weeks Old)
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