Clinical Trial of Group ACYW135 Meningococcal Polysaccharide Vaccine 003
Primary Purpose
Meningitis
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
ACYW135 Meningococcal Polysaccharide Vaccine
A+C Meningococcal Polysaccharide Vaccine
Sponsored by
About this trial
This is an interventional prevention trial for Meningitis focused on measuring Group ACYW135 Meninigococcal Polysaccharide Vaccine
Eligibility Criteria
Inclusion Criteria:
- Healthy permanent residence 2 years of age and older, the subjects (or their guardians) are able to understand and sign the informed consent;
- Healthy male or female by oral history, physical examination and clinical judgment and who complies with vaccination of this product;
- Be able to comply with the requirements of clinical trial protocol and immunogenicity examination;
- Have no history of vaccination within the past 3 months and vaccination with other products within the last 2 weeks;
- Axillary temperature ≤37.0℃.
Exclusion Criteria:
- Any acute disease, such as: tumor, autoimmunity disease, progressive atherosclerotic disease or diabetes with complication, chronic obstructive pulmonary disease need oxygen uptake, acute or progressive hepatopathy or nephropathy, congestive heart-failure, etc.;
- Allergic to vaccines or drugs (history of allergy to any vaccine in the past);
- History of neurologic symptom or signs;
- Known or suspected (or high risk) impaired or abnormal immune function, e.g.: receive immunosuppressant or immunopotentiator therapy, take immunoglobulin or blood product or plasma extract (except the gastrointestinal tract) within the past 3 months, HIV infection or related disease, etc.;
- History of meningitis infection or vaccination of meningococcal vaccine within the past 3 months;
- History of receiving other vaccines or immunoglobulin injection or any research drugs;
- Any acute disease needing application of antibiotics or anti-virus treatment in the whole body within the past 1 week;
- History of fever within the past 3 days (axillary temperature ≥38.0℃);
- Participating in another clinical trial;
- History of allergy, eclampsia, epilepsy, encephalopathy and mental disease or family disease;
- Thrombopenia or other coagulopathy that may cause contraindication to intramuscular injection;
- Acute chronic disease (such as Down syndrome, diabetes, sickle cell anemia or neurologic disease, Guillain-Barre Syndrome);
- Known or suspected diseases, including: respiratory system disease, acute infection or active stage of chronic disease, SBAV infection of children or mothers, cardiovascular disease, acute hypertension, cancer treatment, skin disease, etc.;
- Pregnancy
- Any condition that, in the judgment of investigator, may affect trial assessment.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
ACYW135 Meningococcal Vaccine
A+C Meningococcal Vaccine
Arm Description
0.5 ml/ dose, containing 50 μg of each antigen; lot No.: 20040601, manufacturing date: June 9, 2004 and the expiration date: till June 2006
0.5 ml/ dose; each ampoule or dose contains 100 μg (one single human dose) and 50 μg of each antigen; lot No.: 20050805 and the expiration date: Aug. 24, 2007
Outcomes
Primary Outcome Measures
Safety
Systemic and local adverse reactions after the vaccination; adverse events
Secondary Outcome Measures
Immunogenicity
4-fold (seroconversion) and 8-fold increase of bactericidin; GMT and bactericidin increase after immunization
Full Information
NCT ID
NCT01661751
First Posted
August 3, 2012
Last Updated
August 6, 2012
Sponsor
Hualan Biological Engineering, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT01661751
Brief Title
Clinical Trial of Group ACYW135 Meningococcal Polysaccharide Vaccine 003
Official Title
Phase III Clinical Trial of Group ACYW135 Meningococcal Polysaccharide Vaccine
Study Type
Interventional
2. Study Status
Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
May 2006 (undefined)
Primary Completion Date
May 2006 (Actual)
Study Completion Date
August 2006 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hualan Biological Engineering, Inc.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The clinical trial was designed to evaluate the safety and immunogenicity against Group ACYW135 Meningococcal Polysaccharide Vaccine of Hualan administered on subjects 2 years of age and older.
Detailed Description
Complying with requirements of the approval letter of clinical trial issued by SFDA (Approval Letter No.: 2006L01017), Hualan conducted phase III clinical trial of Group ACYW135 Meningococcal Polysaccharide Vaccine to evaluate the safety and immunogenicity of the experimental vaccine.
The safety end points were the presence of any systemic, local and adverse reaction. Evaluation indicators of immunogenicity were bacteriocin levels of groups A, C, Y and W135 respectively in the serum after the whole vaccination.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Meningitis
Keywords
Group ACYW135 Meninigococcal Polysaccharide Vaccine
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
900 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ACYW135 Meningococcal Vaccine
Arm Type
Experimental
Arm Description
0.5 ml/ dose, containing 50 μg of each antigen; lot No.: 20040601, manufacturing date: June 9, 2004 and the expiration date: till June 2006
Arm Title
A+C Meningococcal Vaccine
Arm Type
Active Comparator
Arm Description
0.5 ml/ dose; each ampoule or dose contains 100 μg (one single human dose) and 50 μg of each antigen; lot No.: 20050805 and the expiration date: Aug. 24, 2007
Intervention Type
Biological
Intervention Name(s)
ACYW135 Meningococcal Polysaccharide Vaccine
Other Intervention Name(s)
Hualan Bio
Intervention Description
600 subjects were divided into three groups (200 subjects in each group), adult (16~30 years of age), early youth (7~15 years of age) and children (2~6 years of age) to receive Group ACYW135 Meningococcal Polysaccharide Vaccine, 0.5 ml, one dose regime
Intervention Type
Biological
Intervention Name(s)
A+C Meningococcal Polysaccharide Vaccine
Other Intervention Name(s)
Lanzhou Institute
Intervention Description
300 subjects were divided into three groups (100 subjects in each group), adult (16~30 years of age), early youth (7~15 years of age) and children (2~6 years of age) to receive Group AC Meningococcal Polysaccharide Vaccine, 0.5 ml, one dose regime
Primary Outcome Measure Information:
Title
Safety
Description
Systemic and local adverse reactions after the vaccination; adverse events
Time Frame
Dat 28 after vaccination
Secondary Outcome Measure Information:
Title
Immunogenicity
Description
4-fold (seroconversion) and 8-fold increase of bactericidin; GMT and bactericidin increase after immunization
Time Frame
The 4th week after immunization
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy permanent residence 2 years of age and older, the subjects (or their guardians) are able to understand and sign the informed consent;
Healthy male or female by oral history, physical examination and clinical judgment and who complies with vaccination of this product;
Be able to comply with the requirements of clinical trial protocol and immunogenicity examination;
Have no history of vaccination within the past 3 months and vaccination with other products within the last 2 weeks;
Axillary temperature ≤37.0℃.
Exclusion Criteria:
Any acute disease, such as: tumor, autoimmunity disease, progressive atherosclerotic disease or diabetes with complication, chronic obstructive pulmonary disease need oxygen uptake, acute or progressive hepatopathy or nephropathy, congestive heart-failure, etc.;
Allergic to vaccines or drugs (history of allergy to any vaccine in the past);
History of neurologic symptom or signs;
Known or suspected (or high risk) impaired or abnormal immune function, e.g.: receive immunosuppressant or immunopotentiator therapy, take immunoglobulin or blood product or plasma extract (except the gastrointestinal tract) within the past 3 months, HIV infection or related disease, etc.;
History of meningitis infection or vaccination of meningococcal vaccine within the past 3 months;
History of receiving other vaccines or immunoglobulin injection or any research drugs;
Any acute disease needing application of antibiotics or anti-virus treatment in the whole body within the past 1 week;
History of fever within the past 3 days (axillary temperature ≥38.0℃);
Participating in another clinical trial;
History of allergy, eclampsia, epilepsy, encephalopathy and mental disease or family disease;
Thrombopenia or other coagulopathy that may cause contraindication to intramuscular injection;
Acute chronic disease (such as Down syndrome, diabetes, sickle cell anemia or neurologic disease, Guillain-Barre Syndrome);
Known or suspected diseases, including: respiratory system disease, acute infection or active stage of chronic disease, SBAV infection of children or mothers, cardiovascular disease, acute hypertension, cancer treatment, skin disease, etc.;
Pregnancy
Any condition that, in the judgment of investigator, may affect trial assessment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fubao Ma, Bachelor
Organizational Affiliation
Immunization Program Institute of Jiangsu Provincial Center for Disease Control and Prevention
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Clinical Trial of Group ACYW135 Meningococcal Polysaccharide Vaccine 003
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