search
Back to results

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
Walvax Biotechnology Co., Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diseases Caused by Streptococcus Pneumoniae Serotypes

Eligibility Criteria

2 Months - 71 Months (Child)All SexesAccepts Healthy Volunteers

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

    First Posted
    March 31, 2016
    Last Updated
    October 11, 2020
    Sponsor
    Walvax Biotechnology Co., Ltd.
    search

    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)

    We'll reach out to this number within 24 hrs