A Booster Dose of Inactivated Vaccine (Vero Cell) Against EV71 in Chinese Children

NCT ID: NCT01734408

Last Updated: 2013-10-23

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

773 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-11-30

Study Completion Date

2013-02-28

Brief Summary

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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 phase II study of inactivated vaccine (vero cell) against EV71 has completed last month in Jiangsu Province in China. The data from the phase II study suggested that the inactivated EV71 vaccine had a clinically acceptable safety and good immunogenicity for healthy Chinese children and infants. But the antibody titer against EV71 was found decreased significantly at month 8 compared to that at day 56. Considering the similar dynamic trend had also been found in the antibody against poliovirus induced by polio vaccines, and whose immunization schedule contains a booster dose administrated at 1 to 1.5 year after the first 3 doses of fundamental immunity. In order to find a better immunization schedule for children, the investigators decided to perform this booster immunity trial among these children who had received two doses of EV71 vaccines (around one year after the fundamental immunity). The investigators do the recruitment among these children who had participated in the previous phase II trial and received EV71 vaccines, and randomize them in a ratio of 2:1 to receive either a booster dose of EV71 vaccines or placebo.

Detailed Description

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Conditions

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EV71-associated Disease

Keywords

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immunogenicity safety inactivated EV71 vaccine

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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alum-adjuvant 160U /0.5ml EV71 vaccine

A booster dose of alum-adjuvant 160U /0.5ml EV71 vaccine in 160 children whom had received two doses of alum-adjuvant 160U/0.5ml EV71 vaccines one year before.

Group Type EXPERIMENTAL

alum-adjuvant 160U /0.5ml

Intervention Type BIOLOGICAL

inactivated vaccine (vero cell) alum-adjuvant 160U /0.5ml EV71 vaccine

placebo A

A 0/0.5ml placebo in 80 children whom had received two doses of alum-adjuvant 160U/0.5ml EV71 vaccines one year before.

Group Type PLACEBO_COMPARATOR

0/0.5ml placebo

Intervention Type BIOLOGICAL

0/0.5ml placebo

alum-adjuvant 320U /0.5ml EV71 vaccine

A booster dose of alum-adjuvant 320U /0.5ml EV71 vaccine in 160 children whom had received two doses of alum-adjuvant 320U/0.5ml EV71 vaccines one year before.

Group Type EXPERIMENTAL

alum-adjuvant 320U /0.5ml

Intervention Type BIOLOGICAL

inactivated vaccine (vero cell) alum-adjuvant 320U /0.5ml EV71 vaccine

placebo B

A 0/0.5ml placebo in 80 children whom had received two doses of alum-adjuvant 320U/0.5ml EV71 vaccines one year before.

Group Type PLACEBO_COMPARATOR

0/0.5ml placebo

Intervention Type BIOLOGICAL

0/0.5ml placebo

alum-adjuvant 640U /0.5ml EV71 vaccine

A booster dose of alum-adjuvant 640U /0.5ml EV71 vaccine in 160 children whom had received two doses of alum-adjuvant 640U/0.5ml EV71 vaccines one year before.

Group Type EXPERIMENTAL

alum-adjuvant 640U /0.5ml

Intervention Type BIOLOGICAL

inactivated vaccine (vero cell) alum-adjuvant 640U /0.5ml EV71 vaccine

placebo C

A 0/0.5ml placebo in 80 children whom had received two doses of alum-adjuvant 640U/0.5ml EV71 vaccines one year before.

Group Type PLACEBO_COMPARATOR

0/0.5ml placebo

Intervention Type BIOLOGICAL

0/0.5ml placebo

adjuvant-free 640U /0.5ml EV71 vaccine

A booster dose of adjuvant-free 640U /0.5ml EV71 vaccine in 160 children whom had received two doses of adjuvant-free 640U/0.5ml EV71 vaccines one year before.

Group Type EXPERIMENTAL

adjuvant-free 640U /0.5ml

Intervention Type BIOLOGICAL

inactivated vaccine (vero cell) adjuvant-free 640U /0.5ml EV71 vaccine

placebo D

A 0/0.5ml placebo in 80 children whom had received two doses of adjuvant-free 640U/0.5ml EV71 vaccines one year before.

Group Type PLACEBO_COMPARATOR

0/0.5ml placebo

Intervention Type BIOLOGICAL

0/0.5ml placebo

Interventions

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alum-adjuvant 160U /0.5ml

inactivated vaccine (vero cell) alum-adjuvant 160U /0.5ml EV71 vaccine

Intervention Type BIOLOGICAL

alum-adjuvant 320U /0.5ml

inactivated vaccine (vero cell) alum-adjuvant 320U /0.5ml EV71 vaccine

Intervention Type BIOLOGICAL

alum-adjuvant 640U /0.5ml

inactivated vaccine (vero cell) alum-adjuvant 640U /0.5ml EV71 vaccine

Intervention Type BIOLOGICAL

adjuvant-free 640U /0.5ml

inactivated vaccine (vero cell) adjuvant-free 640U /0.5ml EV71 vaccine

Intervention Type BIOLOGICAL

0/0.5ml placebo

0/0.5ml placebo

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Had participated in the previous phase II trial and received at least 1 dose of EV71 vaccine.
* Healthy children as established by medical history and clinical examination
* The subjects' guardians are able to understand and sign the informed consent
* Subjects who can and will comply with the requirements of the protocol
* Subjects with temperature \<=37.0°C on axillary setting

Exclusion Criteria

* Had participated in the previous phase II trial and received placebo.
* Subject who has a medical history of EV71-associated disease with specific laboratory evidence
* \<= 37 weeks gestation
* Subjects with a birth weight \<2.5 kg
* Subject that has a medical history of any of the following: allergic history, or allergic to any ingredient of vaccine
* Family history of seizures or progressive neurological disease
* Family history of congenital or hereditary immunodeficiency
* Severe malnutrition or dysgenopathy
* Major congenital defects or serious chronic illness, including perinatal brain damage
* Autoimmune disease
* Bleeding disorder diagnosed by a doctor or significant bruising or bleeding difficulties with IM injections or blood draws
* Any acute infections in last 7 days
* Any prior administration of immunodepressant or corticosteroids in last 6month
* Any prior administration of blood products in last 3 month
* Any prior administration of other research medicines in last 1 month
* Any prior administration of attenuated live vaccine in last 14 days
* Any prior administration of subunit or inactivated vaccines in last 7 days, such as pneumococcal vaccine
* Under the anti-TB prevention or therapy
* Any condition that in the opinion of the investigator, may interfere with the evaluation of study objectives
Minimum Eligible Age

21 Months

Maximum Eligible Age

51 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bejing Vigoo Biological Co., LTD

INDUSTRY

Sponsor Role collaborator

Jiangsu Province Centers for Disease Control and Prevention

NETWORK

Sponsor Role lead

Responsible Party

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Fengcai Zhu

vice director

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Jiangsu Provincial Center for Diseases Control and Prevention

Nanjing, Jiangsu, China

Site Status

Countries

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China

References

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Shenyu W, Jingxin L, Zhenglun L, Xiuling L, Qunying M, Fanyue M, Hua W, Yuntao Z, Fan G, Qinghua C, Yuemei H, Xin Y, Huijie G, Fengcai Z. A booster dose of an inactivated enterovirus 71 vaccine in chinese young children: a randomized, double-blind, placebo-controlled clinical trial. J Infect Dis. 2014 Oct 1;210(7):1073-82. doi: 10.1093/infdis/jiu113. Epub 2014 Mar 12.

Reference Type DERIVED
PMID: 24625805 (View on PubMed)

Other Identifiers

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JSVCT005b

Identifier Type: -

Identifier Source: org_study_id