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
About this trial
This is an interventional prevention trial for Hand Foot and Mouth Disease focused on measuring vaccine, safety, immunogenicity
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.
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
NCT ID
NCT02889497
First Posted
August 31, 2016
Last Updated
September 6, 2016
Sponsor
Beijing Chaoyang District Centre for Disease Control and Prevention
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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