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Immunogenicity and Safety of Inactivated and Live Attenuated Hepatitis A Vaccines

J

Jiangsu Provincial Center for Disease Control and Prevention

Status and phase

Completed
Phase 4

Conditions

Hepatitis A

Treatments

Biological: Attenuated Hepatitis A Vaccine, H2 Strain
Biological: Group A Meningococcal Polysaccharide vaccine
Biological: Inactivated Hepatitis A Vaccine, Lu8 Strain

Study type

Interventional

Funder types

Other
NETWORK

Identifiers

NCT02601040
JSEPI-004

Details and patient eligibility

About

The main purpose of this study was to evaluate the safety and immunogenicity of Immunogenicity of Inactivated and Live Attenuated Hepatitis A Vaccines for healthy Chinese people.

Enrollment

13,500 patients

Sex

All

Ages

18 months to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Only subjects fulfilling all of the following criteria will be eligible for the study:
  • People aged from 18 months to 65 years old.
  • The subjects or subjects' guardians are able to understand and sign the informed consent
  • The subjects or subjects' guardians allow to comply with the requirements of the protocol
  • Subjects with temperature <=37.0°C on axillary setting
  • The subjects have signed informed consent already

Exclusion criteria

  • Subjects will not be eligible for the study if any of the following criteria is met:
  • Subject who has a medical history of serious disease including Tumor, autoimmune disease, progressive atherosclerosis diseases or complications of diabetes, chronic obstructive pulmonary disease (copd), kidney disease, congestive heart failure etc.
  • Have a history of neurological symptoms or signs
  • Have medical history or family history relating to allergies, seizures, epilepsy, brain and spirit etc.
  • Suffering from serious chronic diseases
  • Suffering from known or suspected of diseases including respiratory diseases, acute infection , mothers have HIV infection, cardiovascular disease, severe hypertension, skin diseases, malignant tumor
  • Allergic to any ingredient in research, history of allergies to any vaccination (always), especially for people allergic to high protein food like eggs and milk
  • Any prior known or suspected damage or abnormal immune function. As for patients who are treated with immune inhibitors or immune enhancer medicine, accept with immunoglobin, blood products and plasma extraction within 3 months
  • Any prior diseases including human immunodeficiency virus infection or related
  • Bleeding constitution or prolong bleeding time situation
  • Accept hepatitis A vaccination within a month
  • Received vaccines, other immune globulin, any research drug injections in the past 4 weeks
  • People who had any acute illness, needed systemic antibiotics or antiviral treatment in the past 7 days
  • Caught a fever with axillary temperature 38°C or higher in past 3 days
  • Take part in another clinical researchers
  • Any medical, psychiatric, social condition, occupational reason or other responsibility that, in the judgment of the investigator, is a contraindication to protocol participation or impairs a volunteer's ability to give informed consent
  • Pregnancy test result is positive

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

13,500 participants in 3 patient groups, including a placebo group

Attenuated Hepatitis A Vaccine, H2 Strain
Experimental group
Description:
Health subjects received attenuated Hepatitis A vaccine intramuscularly in the deltoid region.
Treatment:
Biological: Attenuated Hepatitis A Vaccine, H2 Strain
Inactivated Hepatitis A Vaccine, Lu8 Strain
Experimental group
Description:
Health subjects received inactivated Hepatitis A vaccine intramuscularly in the deltoid region.
Treatment:
Biological: Inactivated Hepatitis A Vaccine, Lu8 Strain
Group A Meningococcal Polysaccharide vaccine
Placebo Comparator group
Description:
Health subjects received Group A Meningococcal Polysaccharide vaccine intramuscularly in the deltoid region.
Treatment:
Biological: Group A Meningococcal Polysaccharide vaccine

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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