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Safety, Three Batches Consistency and Immunity Duration of the Post-marketing Inactivated Enterovirus Type 71 (EV71) Vaccine in Children Aged 6-71 Months

Primary Purpose

Hand Foot and Mouth Disease

Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
the first batch vaccine
the second batch vaccine
the third batch vaccine
Sponsored by
Beijing Chaoyang District Centre for Disease Control and Prevention
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hand Foot and Mouth Disease focused on measuring vaccine, safety, immunogenicity

Eligibility Criteria

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

Inclusion Criteria:

  • 8 Months to 71 Months (Healthy Children or Infants);
  • Providing the subjects' legal identity certificate (birth certificate , residence booklet or ID card) and vaccination certificate, legal guardians can provide legal identity proof (resident booklet or ID card) so that the doctor can determine the subject identity to complete recruitment program;
  • The subjects' guardians are able to understand and sign the informed consent voluntary. Guardians have the ability to use the thermometer ,dividing ruler and can fill out the Diary card ,follow-up card according to requirements;
  • Persist for a 24 months visit.If doubtful HFMD case happen,the subject's guardian should send the subject to the medical institutions at above the county level and report this case to the investigator.The subjects who participate immunogenicity observation group can receive sample collection including blood,throat swab or anal awab according to program requirements.

Exclusion Criteria:

  • Exclusion Criteria for the first dose:

    • Subject with clinical diagnosis or suspect HFMD(Especially the history of herpangina);
    • Subject that has a medical history of any of the following: allergic history, or allergic to any ingredient of vaccine;
    • History of seizures,convulsions or twitching ;Family history of progressive neurological disease;
    • Autoimmune disease or immunologic deficiency.Any prior administration of immunodepressant in last 6month;
    • History of asthma,thyroid ablation,angioneurotic edema, diabetes mellitus or malignant tumour;
    • Alienia,functional asplenia,or any condition that cause asplenia or splenectomy;
    • Diagnosed coagulation abnormalities (such as clotting factor deficiency, coagulation disorders, platelet disorder) or significant bruising or blood clotting disorder;
    • Any acute disease or chronic disease attack in last 7 days;
    • Any prior administration of blood products in last 3 month;
    • Any prior administration of attenuated live vaccine in last 15 days , subunit or inactivated vaccines in last 7 days;
    • Fever before vaccination, axillary temperature ﹥37.0℃;
    • Attend Other vaccine or drug clinical trials concurrent in 6 months;
    • Any condition that in the opinion of the investigator。
  • Exclusion Criteria for the second dose:

    • Any exclusion criteria for the first dose happens after been enrolled;
    • Newly HFMD diagnosed patients after been enrolled;
    • Any condition that in the opinion of the investigator or ethics committee think should be eliminated.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Experimental

    Arm Label

    300 subjects receive the first batch vaccine

    300 subjects receive the second batch vaccine

    300 subjects receive the third batch vaccine

    Arm Description

    300 subjects will be randomly received the first batch vaccine

    300 subjects will be randomly received the second batch vaccine

    300 subjects will be randomly received the third batch vaccine

    Outcomes

    Primary Outcome Measures

    Evaluate the Rate of Adverse reactions of Post-marketing Inactivated Enterovirus Type 71 (EV71) Vaccine in Children Aged 6-71 Months.
    Adverse reactions associated with vaccine will be observed in Children Aged 6-71 Months 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.
    Evaluate the seroconversion rate of EV71 antibodies in serum after vaccination.
    The seroconversion rate of EV71 antibodies will be evaluated in serum at days 0 and 56.

    Secondary Outcome Measures

    Full Information

    First Posted
    August 31, 2016
    Last Updated
    September 6, 2016
    Sponsor
    Beijing Chaoyang District Centre for Disease Control and Prevention
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02889497
    Brief Title
    Safety, Three Batches Consistency and Immunity Duration of the Post-marketing Inactivated Enterovirus Type 71 (EV71) Vaccine in Children Aged 6-71 Months
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 2016 (undefined)
    Primary Completion Date
    March 2019 (Anticipated)
    Study Completion Date
    September 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Beijing Chaoyang District Centre for Disease Control and Prevention

    4. Oversight

    5. Study Description

    Brief Summary
    This study evaluates the safety,three batches consistency and immunity duration of the post-marketing inactivated Enterovirus Type 71 (EV71) vaccine in children aged 6-71 months.This study has two groups:safety observation group and immunogenicity observation group.20000 subjects will receive 2 doses vaccines and be observed for safety among 2 epidemic cycles of HFMD.In the immunogenicity observation group, 900 subjects will be randomly received 3 batches vaccines(2 doses),and blood sampled at days 0 and 56.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Hand Foot and Mouth Disease
    Keywords
    vaccine, safety, immunogenicity

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    20900 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    300 subjects receive the first batch vaccine
    Arm Type
    Experimental
    Arm Description
    300 subjects will be randomly received the first batch vaccine
    Arm Title
    300 subjects receive the second batch vaccine
    Arm Type
    Experimental
    Arm Description
    300 subjects will be randomly received the second batch vaccine
    Arm Title
    300 subjects receive the third batch vaccine
    Arm Type
    Experimental
    Arm Description
    300 subjects will be randomly received the third batch vaccine
    Intervention Type
    Biological
    Intervention Name(s)
    the first batch vaccine
    Intervention Type
    Biological
    Intervention Name(s)
    the second batch vaccine
    Intervention Type
    Biological
    Intervention Name(s)
    the third batch vaccine
    Primary Outcome Measure Information:
    Title
    Evaluate the Rate of Adverse reactions of Post-marketing Inactivated Enterovirus Type 71 (EV71) Vaccine in Children Aged 6-71 Months.
    Description
    Adverse reactions associated with vaccine will be observed in Children Aged 6-71 Months 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.
    Time Frame
    24 months
    Title
    Evaluate the seroconversion rate of EV71 antibodies in serum after vaccination.
    Description
    The seroconversion rate of EV71 antibodies will be evaluated in serum at days 0 and 56.
    Time Frame
    56 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    6 Months
    Maximum Age & Unit of Time
    71 Months
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: 8 Months to 71 Months (Healthy Children or Infants); Providing the subjects' legal identity certificate (birth certificate , residence booklet or ID card) and vaccination certificate, legal guardians can provide legal identity proof (resident booklet or ID card) so that the doctor can determine the subject identity to complete recruitment program; The subjects' guardians are able to understand and sign the informed consent voluntary. Guardians have the ability to use the thermometer ,dividing ruler and can fill out the Diary card ,follow-up card according to requirements; Persist for a 24 months visit.If doubtful HFMD case happen,the subject's guardian should send the subject to the medical institutions at above the county level and report this case to the investigator.The subjects who participate immunogenicity observation group can receive sample collection including blood,throat swab or anal awab according to program requirements. Exclusion Criteria: Exclusion Criteria for the first dose: Subject with clinical diagnosis or suspect HFMD(Especially the history of herpangina); Subject that has a medical history of any of the following: allergic history, or allergic to any ingredient of vaccine; History of seizures,convulsions or twitching ;Family history of progressive neurological disease; Autoimmune disease or immunologic deficiency.Any prior administration of immunodepressant in last 6month; History of asthma,thyroid ablation,angioneurotic edema, diabetes mellitus or malignant tumour; Alienia,functional asplenia,or any condition that cause asplenia or splenectomy; Diagnosed coagulation abnormalities (such as clotting factor deficiency, coagulation disorders, platelet disorder) or significant bruising or blood clotting disorder; Any acute disease or chronic disease attack in last 7 days; Any prior administration of blood products in last 3 month; Any prior administration of attenuated live vaccine in last 15 days , subunit or inactivated vaccines in last 7 days; Fever before vaccination, axillary temperature ﹥37.0℃; Attend Other vaccine or drug clinical trials concurrent in 6 months; Any condition that in the opinion of the investigator。 Exclusion Criteria for the second dose: Any exclusion criteria for the first dose happens after been enrolled; Newly HFMD diagnosed patients after been enrolled; Any condition that in the opinion of the investigator or ethics committee think should be eliminated.

    12. IPD Sharing Statement

    Learn more about this trial

    Safety, Three Batches Consistency and Immunity Duration of the Post-marketing Inactivated Enterovirus Type 71 (EV71) Vaccine in Children Aged 6-71 Months

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