Hand, foot, and mouth disease (HFMD) is a common viral illness in infants and children caused by viruses that belong to the enterovirus genus of the picornavirus family. Although most HFMD cases do not result in serious complications, outbreaks of HFMD caused by enterovirus 71 (EV71) can present with a high rate of neurological complications, including meningoencephalitis, pulmonary complications, and can even cause infant death. HFMD caused by EV71 has become a major emerging infectious disease in Asia and the highly pathogenic potential of EV71 clearly requires the attention of world medical community. The development of vaccine against EV71 is active and ongoing in Asian countries now. Several studies have examined the effectiveness of inactivated viral vaccines against EV71 in animal model. A wide range of experimental EV71 vaccine approaches have been studied including heat-inactivated or formaldehyde-inactivated virion, EV71 virus-like particles (VLP) , VP1 recombinant protein ,VP1 DNA vaccine , VP1 peptide-based vaccine targeting the neutralizing domain, bacterial or viral vector expressing VP1, and a Vero cell-adapted live attenuated virus. Furthermore, neutralizing antibodies against EV71 have been suggested as one of the most important factors in prevention of the severe EV71 infection. Recently, an inactivated vaccine(vero cell) against EV71 has been licensed by SFDA in China, this clinical trial phase Ia is armed to evaluate safety and tolerance in Chinese healthy adults and children.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
100
inactivated vaccine(vero cell) against EV71 of 320U/0.5ml on day0,28,modern medicines
inactivated vaccine(vero cell) against EV71 of 640U/0.5ml on day0,28
inactivated vaccine(vero cell) against EV71 of 160U/0.5ml on 0,28 day
inactivated vaccine(vero cell) against EV71 of 320U/0.5ml on day0,28
inactivated vaccine(vero cell) against EV71 of 640U/0.5ml on day0,28
to evaluate the safety of EV71 vaccine in Chinese healthy adults and children
to evaluate the Adverse reactions of EV71 vaccine in Chinese healthy adults and children
Time frame: 28 days after the first vaccination
to evaluate the safety of EV71 vaccine in Chinese healthy adults and children
to evaluate the Adverse reactions of EV71 vaccine in Chinese healthy adults and children
Time frame: 28 days after the second vaccination
to evaluate the seroconversion rate of Antinuclear antibodies in serum after first vaccination
to evaluate the seroconversion rate of Antinuclear antibodies in serum 28 days after first vaccination
Time frame: 28 days after the first vaccination
to evaluate the seroconversion rate of Antinuclear antibodies in serum after second vaccination
to evaluate the seroconversion rate of Antinuclear antibodies in serum 28 days after second vaccination
Time frame: 28 days after second vaccination
to evaluate the abnormity change of live and kidney function indexes in serum after first vaccination
to evaluate the abnormity change of live and kidney function indexes in serum 3 days after first vaccination
Time frame: 3 days after first vaccination
to evaluate the abnormity change of live and kidney function indexes in serum after second vaccination
to evaluate the abnormity change of live and kidney function indexes in serum 3 days after second vaccination
Time frame: 3 days after second vaccination
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