A Clinical Trial for Inactivated Japanese Encephalitis Vaccine in Healthy Chinese Infants
NCT ID: NCT02367664
Last Updated: 2016-09-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
900 participants
INTERVENTIONAL
2014-10-31
2016-06-30
Brief Summary
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Detailed Description
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In order to evaluate immunogenicity and safety of Vero cell-derived inactivated Japanese Encephalitis vaccine produced by Shandong Hengye Biotech Co., Ltd. a single-centre phase III clinical trial is planned to conduct in healthy infants aged 6-11 months in China.
There will be two immunization programs. 600 healthy infants aged 6-11 months will be randomly assigned (1:1) to receive an experimental vaccine or a positive control vaccine at day 0,7. Another 300 healthy infants aged 6-11 months will be recruited to receive an experimental vaccine at day 0,28. All of them will be received a third dose as booster vaccination 12 months later.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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0.5ml experimental vaccine on day 0,7
0.5ml experimental vaccine on day 0,7 and a booster dose 12 months later
0.5ml experimental vaccine on day 0,7 Vero cell-derived inactivated Japanese Encephalitis vaccine
Vero cell-derived inactivated Japanese Encephalitis vaccine produced by Shandong Hengye Biotech Co., Ltd./0.5ml, two doses with 7 days interval, a booster dose 12 months after the first dose
0.5ml experimental vaccine on day 0,28
0.5ml experimental vaccine on day 0,28 and a booster dose 12 months later
0.5ml experimental vaccine on day 0,28 Vero cell-derived inactivated Japanese Encephalitis vaccine
Vero cell-derived inactivated Japanese Encephalitis vaccine produced by Shandong Hengye Biotech Co., Ltd./0.5ml, two doses with 28 days interval, a booster dose 12 months after the first dose
0.5ml active comparator vaccine on day 0,7
0.5ml active comparator vaccine on day 0,7 and a booster dose 12 months later
0.5ml active comparator vaccine on day 0,7 inactivated freeze-dried Japanese Encephalitis vaccine(Vero cell)
inactivated freeze-dried Japanese Encephalitis vaccine(Vero cell) produced by Beijing Tiantan Biological Products Co., Ltd. /0.5ml, two doses with 7 days interval, a booster dose 12 months after the first dose
Interventions
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0.5ml experimental vaccine on day 0,7 Vero cell-derived inactivated Japanese Encephalitis vaccine
Vero cell-derived inactivated Japanese Encephalitis vaccine produced by Shandong Hengye Biotech Co., Ltd./0.5ml, two doses with 7 days interval, a booster dose 12 months after the first dose
0.5ml experimental vaccine on day 0,28 Vero cell-derived inactivated Japanese Encephalitis vaccine
Vero cell-derived inactivated Japanese Encephalitis vaccine produced by Shandong Hengye Biotech Co., Ltd./0.5ml, two doses with 28 days interval, a booster dose 12 months after the first dose
0.5ml active comparator vaccine on day 0,7 inactivated freeze-dried Japanese Encephalitis vaccine(Vero cell)
inactivated freeze-dried Japanese Encephalitis vaccine(Vero cell) produced by Beijing Tiantan Biological Products Co., Ltd. /0.5ml, two doses with 7 days interval, a booster dose 12 months after the first dose
Eligibility Criteria
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Inclusion Criteria
* Had never received any Japanese Encephalitis vaccine
* Subjects' legal guardians are able to understand and sign the informed consent
* In good general health judged from medical history and clinical examination at the time of inclusion
* Subjects and legal guardians can and will comply with the requirements of the protocol
* Subjects with temperature \<=37.0°C on axillary setting
Exclusion Criteria
* Subject who is allergic to any ingredient of the vaccine
* Family history of congenital or hereditary immunodeficiency
* Subject with damaged or low immune function which has already been known
* Subject who had a Japanese Encephalitis medical history
* Subject with acute febrile illness or infectious disease
* Major congenital defects or serious chronic illness, including perinatal brain damage
* Thrombocytopenia, blood coagulation disorder or bleeding difficulties with intramuscular injection
* Subject who has serious allergic history
* Subject with other medical history not suitable for vaccination such as fainting during injection or acupuncture treatment
* Any prior administration of immunodepressant or corticosteroids in last 6 months
* Any prior administration of blood products in last 3 months
* Any prior administration of other research medicine/vaccine in last 30 days
* Any prior administration of any attenuated live vaccine in last 30 days
* Any prior administration of subunit or inactivated vaccines in last 14 days, such as pneumococcal vaccine
* Any acute infection or serious infection needing systemic antibiotics or antiviral treatment in last 7 days
* Any fever with temperature \>=38.0°C on axillary setting in last 3 days
* Any medical, psychological, social or other condition judged by investigator, that may interfere subject's compliance with the protocol or signature on informed consent
6 Months
11 Months
ALL
Yes
Sponsors
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Shandong Hengye Biotech Co., Ltd.
UNKNOWN
Jiangsu Province Centers for Disease Control and Prevention
NETWORK
Responsible Party
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Locations
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Pizhou Center for Disease Control and Prevention
Xuzhou, Jiangsu, China
Countries
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Other Identifiers
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JSVCT015
Identifier Type: -
Identifier Source: org_study_id
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