search
Back to results

Immunogenicity and Safety of Meningococcal ACYW135 Polysaccharide Conjugate Vaccine in Volunteers Aged From 3 to 35 Months

Primary Purpose

Meningitis, Meningococcal

Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Meningococcal ACYW135 Polysaccharide Conjugate Vaccine
Meningococcal ACYW135 Polysaccharide Conjugate Vaccine
Sponsored by
Beijing Zhifei Lvzhu Biopharmaceutical Co., Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Meningitis, Meningococcal

Eligibility Criteria

3 Months - 35 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • People aged 3-35 months;
  • Subject who has not been vaccinated with meningococcal group A and C conjugate vaccine, meningococcal group A polysaccharide vaccine and meningococcal group A and C and haemophilus b conjugate vaccine at the aged of 3-11 months, and who have't given boost immunity above 1 year old, and they all meet the physical examination requirements of the project;
  • Infants aged 3-11 months should be full-term (37-42 weeks of gestation) and their birth weight should meet the requirements (2500g ≤ body weight ≤ 4000g);
  • The guardian signs the informed consent form;
  • The guardian and his family agree to comply with the requirements of the clinical trial protocol;
  • Subject who had no history of other live vaccines within 14 days before vaccination and no history of other inactivated vaccines within 7 days;
  • Axillary body temperature ≤ 37.0 ℃.

Exclusion Criteria:

  • History of severe allergic reactions requiring medical intervention (such as swelling of mouth and throat, dyspnea, hypotension or shock);
  • Have a history of allergy to the vaccine or vaccine ingredients (especially those allergic to tetanus toxoid), or have a history of other serious adverse reactions to the vaccine;
  • A clearly diagnosed history of thrombocytopenia or other coagulation disorders that may cause contraindications to intramuscular injection;
  • Abnormal production process, asphyxia rescue history, or congenital malformation, developmental disorder or serious chronic disease;
  • Has serious cardiovascular, liver and kidney diseases or congenital abnormalities and HIV infection;
  • Suffer from encephalopathy, uncontrolled epilepsy, convulsion and other progressive nervous system diseases;
  • Acute disease, severe chronic disease, acute attack of chronic disease and fever (axillary body temperature ≥ 38.0 ℃) in the past 3 days;
  • Plan to participate or be participating in any other drug clinical research;
  • The interval between the first dose of test vaccine and meningococcal group A polysaccharide vaccine is less than 28 days;
  • According to the judgment of the investigator, the subject has any other factors that are not suitable for participating in the clinical trial.

Sites / Locations

  • Rongan Center for Disease Control and Prevention

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

High dose Group

Low dose Group

Arm Description

Meningococcal ACYW135 Polysaccharide Conjugate Vaccine, 40μg/dose

Received Vaccine: Meningococcal ACYW135 Polysaccharide Conjugate Vaccine, 20μg/dose

Outcomes

Primary Outcome Measures

Immunogenicity study of Meningococcal ACYW135 Polysaccharide Conjugate Vaccine as assessed by positive conversion rate
Safety study of Meningococcal ACYW135 Polysaccharide Conjugate Vaccine as assessed by the occurrence of adverse events
Evaluate the incidence of adverse reactions for Meningococcal ACYW135 Polysaccharide Conjugate Vaccine

Secondary Outcome Measures

Full Information

First Posted
January 28, 2022
Last Updated
February 9, 2022
Sponsor
Beijing Zhifei Lvzhu Biopharmaceutical Co., Ltd
search

1. Study Identification

Unique Protocol Identification Number
NCT05229536
Brief Title
Immunogenicity and Safety of Meningococcal ACYW135 Polysaccharide Conjugate Vaccine in Volunteers Aged From 3 to 35 Months
Official Title
A Single-center, Randomized, Double-blind, Parallel Control Phase II Clinical Trial to Evaluate Immunogenicity and Safety of Meningococcal ACYW135 Polysaccharide Conjugate Vaccine in Healthy Volunteers Aged From 3 to 35 Months
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
December 21, 2018 (Actual)
Primary Completion Date
November 21, 2019 (Actual)
Study Completion Date
November 21, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Beijing Zhifei Lvzhu Biopharmaceutical Co., Ltd

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the immunogenicity and safety of Meningococcal ACYW135 Polysaccharide Conjugate Vaccine in healthy volunteers aged from 3 months to 35 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Meningitis, Meningococcal

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
720 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High dose Group
Arm Type
Experimental
Arm Description
Meningococcal ACYW135 Polysaccharide Conjugate Vaccine, 40μg/dose
Arm Title
Low dose Group
Arm Type
Experimental
Arm Description
Received Vaccine: Meningococcal ACYW135 Polysaccharide Conjugate Vaccine, 20μg/dose
Intervention Type
Biological
Intervention Name(s)
Meningococcal ACYW135 Polysaccharide Conjugate Vaccine
Intervention Description
Group 1: 3/2/1 dose(s) according to age of subjects. Single intramuscular dose contains 10 µg each of Serogroup A, C, Y, and W135 polysaccharide conjugate.
Intervention Type
Biological
Intervention Name(s)
Meningococcal ACYW135 Polysaccharide Conjugate Vaccine
Intervention Description
Group 2: 3/2/1 dose(s) according to age of subjects. Single intramuscular dose contains 5 µg each of Serogroup A, C, Y, and W135 polysaccharide conjugate.
Primary Outcome Measure Information:
Title
Immunogenicity study of Meningococcal ACYW135 Polysaccharide Conjugate Vaccine as assessed by positive conversion rate
Time Frame
30 day after each vaccination
Title
Safety study of Meningococcal ACYW135 Polysaccharide Conjugate Vaccine as assessed by the occurrence of adverse events
Description
Evaluate the incidence of adverse reactions for Meningococcal ACYW135 Polysaccharide Conjugate Vaccine
Time Frame
30 day after each vaccination

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Months
Maximum Age & Unit of Time
35 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: People aged 3-35 months; Subject who has not been vaccinated with meningococcal group A and C conjugate vaccine, meningococcal group A polysaccharide vaccine and meningococcal group A and C and haemophilus b conjugate vaccine at the aged of 3-11 months, and who have't given boost immunity above 1 year old, and they all meet the physical examination requirements of the project; Infants aged 3-11 months should be full-term (37-42 weeks of gestation) and their birth weight should meet the requirements (2500g ≤ body weight ≤ 4000g); The guardian signs the informed consent form; The guardian and his family agree to comply with the requirements of the clinical trial protocol; Subject who had no history of other live vaccines within 14 days before vaccination and no history of other inactivated vaccines within 7 days; Axillary body temperature ≤ 37.0 ℃. Exclusion Criteria: History of severe allergic reactions requiring medical intervention (such as swelling of mouth and throat, dyspnea, hypotension or shock); Have a history of allergy to the vaccine or vaccine ingredients (especially those allergic to tetanus toxoid), or have a history of other serious adverse reactions to the vaccine; A clearly diagnosed history of thrombocytopenia or other coagulation disorders that may cause contraindications to intramuscular injection; Abnormal production process, asphyxia rescue history, or congenital malformation, developmental disorder or serious chronic disease; Has serious cardiovascular, liver and kidney diseases or congenital abnormalities and HIV infection; Suffer from encephalopathy, uncontrolled epilepsy, convulsion and other progressive nervous system diseases; Acute disease, severe chronic disease, acute attack of chronic disease and fever (axillary body temperature ≥ 38.0 ℃) in the past 3 days; Plan to participate or be participating in any other drug clinical research; The interval between the first dose of test vaccine and meningococcal group A polysaccharide vaccine is less than 28 days; According to the judgment of the investigator, the subject has any other factors that are not suitable for participating in the clinical trial.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lin Du
Organizational Affiliation
Beijing Zhifei Lvzhu Biopharmaceutical Co., Ltd
Official's Role
Study Chair
Facility Information:
Facility Name
Rongan Center for Disease Control and Prevention
City
Liuzhou
State/Province
Guangxi
ZIP/Postal Code
530028
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Immunogenicity and Safety of Meningococcal ACYW135 Polysaccharide Conjugate Vaccine in Volunteers Aged From 3 to 35 Months

We'll reach out to this number within 24 hrs