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Safety, Immunogenicity and Reactogenicity Trial of Mencevax ACW135 Vaccine (ETH-TVT)

Primary Purpose

Meningococcal Meningitis

Status
Completed
Phase
Phase 2
Locations
Ethiopia
Study Type
Interventional
Intervention
Mencevax ACW Vaccine
Sponsored by
Armauer Hansen Research Institute, Ethiopia
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Meningococcal Meningitis focused on measuring Trivalent meningococcal polysaccharide vaccine, Children, Safety, Immunogenicity, To assess Safety of trivalent meningococcal polysaccharide vaccine in children, To assess the immunogenicity of the trivalent polysaccharide vaccine in children

Eligibility Criteria

2 Years - 29 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Age between 2-29 years, both sexes, living in the selected villages of Butajira area
  2. A written informed consent signed by the individual (>=18y) or caretaker/guardian (2 to 17 years of age) as 18 is the legal age of maturity in Ethiopia. Assent from children/adolescents aged 12-17 years old.
  3. Free of obvious health problems ascertained by medical history and clinical examination on the day of enrolment

Exclusion Criteria:

  1. Those who are unlikely to complete the follow up at 4-weeks post-vaccination.
  2. Use of any investigational or non-registered drug or vaccine other than the study vaccines within 30 days preceding the first dose of study vaccine, or planned use during the study period.
  3. Administration of blood transfusion within 2 years prior to enrolment or planned use during the study period.
  4. Verbal report of previous vaccination with meningococcal serogroup A, C, Y or W135 vaccines since 1999.
  5. Confirmed or suspected immunosuppressive or immunodeficient condition including HIV infection.
  6. A family history of congenital or hereditary immunodeficiency.
  7. History of allergic reaction to any component of the vaccine
  8. Presence of any fever (defined as axillary temperature of 37.5 degree centigrade or more) and/or severe illness on the day of enrolment/ vaccination.
  9. Pregnancy.
  10. lactation

Sites / Locations

  • Butajira Hospital

Outcomes

Primary Outcome Measures

To evaluate point estimates and trends in immunogenicity after not less than 28 days (+6 days) among children 2 - 4 years as compared to children 5 - 14 years and adolescents/adults 15 - 29 years (all ages inclusive)

Secondary Outcome Measures

To assess the incidence of adverse events following vaccination at 1h, 1d, 2d, 3d, 7d and 28 days post-vaccination.
To assess the immunogenicity at 11 months and 23 months (inclusive) postvaccination.

Full Information

First Posted
October 13, 2009
Last Updated
October 15, 2009
Sponsor
Armauer Hansen Research Institute, Ethiopia
Collaborators
World Health Organization, Addis Ababa University, LSHTM,UK
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1. Study Identification

Unique Protocol Identification Number
NCT00994695
Brief Title
Safety, Immunogenicity and Reactogenicity Trial of Mencevax ACW135 Vaccine
Acronym
ETH-TVT
Official Title
A Phase II Open and Parallel Safety, Immunogenicity and Reactogenicity Trial of Mencevax ACW135 Polysaccharide Vaccine Comparing Three Groups: 2 - 4 Year, 5 - 14 Year and 15 - 29 Year Old Ethiopians
Study Type
Interventional

2. Study Status

Record Verification Date
October 2009
Overall Recruitment Status
Completed
Study Start Date
November 2005 (undefined)
Primary Completion Date
January 2006 (Actual)
Study Completion Date
November 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Armauer Hansen Research Institute, Ethiopia
Collaborators
World Health Organization, Addis Ababa University, LSHTM,UK

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Primary objective: To assess the immunogenicity of the Mencevax ACW135 polysaccharide vaccine at 28 days (+6days) post vaccination in 2-4, 5-14, 15-29 year age groups and compare the immunogenicity between these age groups. Secondary Objectives: To estimate the incidence of common adverse events following immunization (AEFI) of GSK Nm ACW135 polysaccharide vaccine at 1h, 1d, 2d, 3d, 7d and 28 days post-vaccination To assess the persistence of antibody against meningitis A, C and W135 at 11 and 23 months post vaccination in 2-4, 5-14, 15-29 year age groups Study site:Two rural communities (Kebele) in Butajira district, Ethiopia. Methods: Phase II, open and parallel safety and immunogenicity trial. 234 younger children (2-4 years), 145 older children (5-14 years) and 33 adults (15-29 years of age) were randomly selected from the demographic surveillance database and enrolled after screening and consenting. Study participant received Mencevax ACW polysaccharide vaccine 50 mg in 0.5ml subcutaneously. Blood samples for measuring SBA titres were collected at pre vaccination and on day 28 (+6 days) post vaccination. Active follow up for AEFI on post vaccination day 0, 1, 2, 3, 7, & 28. Primary end point was vaccine response defined as sero-conversion (in subjects initially seronegative) or a 4 fold increase (in subjects initially seropositive) in serum bactericidal antibodies (SBA) against serogroups Men A, C and W135) on post vaccination day 28. In addition seroconversion was assessed by ELISA Men A IgG on day 0 and day 28 post vaccination. Secondary endpoints were incidence of general and local symptoms and other adverse events following immunisation during the post vaccination period day 0 to 28 and immune persistence on post vaccination month-11 and month-23. Results: No significant difference in the incidence of general or local AEFI was observed between the age groups The statistical analysis for the Immunogenicity data is in progress

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Meningococcal Meningitis
Keywords
Trivalent meningococcal polysaccharide vaccine, Children, Safety, Immunogenicity, To assess Safety of trivalent meningococcal polysaccharide vaccine in children, To assess the immunogenicity of the trivalent polysaccharide vaccine in children

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Enrollment
412 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
Mencevax ACW Vaccine
Other Intervention Name(s)
Mencevax ACW polysaccharide vaccine
Intervention Description
Mencevax ACW polysaccharide vaccine subcutaneously in the left arm at 50 μg in 0.5ml(reconstituted).
Primary Outcome Measure Information:
Title
To evaluate point estimates and trends in immunogenicity after not less than 28 days (+6 days) among children 2 - 4 years as compared to children 5 - 14 years and adolescents/adults 15 - 29 years (all ages inclusive)
Time Frame
28 days
Secondary Outcome Measure Information:
Title
To assess the incidence of adverse events following vaccination at 1h, 1d, 2d, 3d, 7d and 28 days post-vaccination.
Time Frame
28days
Title
To assess the immunogenicity at 11 months and 23 months (inclusive) postvaccination.
Time Frame
23 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
29 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age between 2-29 years, both sexes, living in the selected villages of Butajira area A written informed consent signed by the individual (>=18y) or caretaker/guardian (2 to 17 years of age) as 18 is the legal age of maturity in Ethiopia. Assent from children/adolescents aged 12-17 years old. Free of obvious health problems ascertained by medical history and clinical examination on the day of enrolment Exclusion Criteria: Those who are unlikely to complete the follow up at 4-weeks post-vaccination. Use of any investigational or non-registered drug or vaccine other than the study vaccines within 30 days preceding the first dose of study vaccine, or planned use during the study period. Administration of blood transfusion within 2 years prior to enrolment or planned use during the study period. Verbal report of previous vaccination with meningococcal serogroup A, C, Y or W135 vaccines since 1999. Confirmed or suspected immunosuppressive or immunodeficient condition including HIV infection. A family history of congenital or hereditary immunodeficiency. History of allergic reaction to any component of the vaccine Presence of any fever (defined as axillary temperature of 37.5 degree centigrade or more) and/or severe illness on the day of enrolment/ vaccination. Pregnancy. lactation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Abraham Aseffa Aseffa, M.D, PhD
Organizational Affiliation
Senior Sientist,Deputy Director, AHRI
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ahmed Bedru Omer, M.D,Pediatrician
Organizational Affiliation
Clinical Trial coordinator,AHRI
Official's Role
Principal Investigator
Facility Information:
Facility Name
Butajira Hospital
City
Butajira
State/Province
Southern Nationality
Country
Ethiopia

12. IPD Sharing Statement

Citations:
PubMed Identifier
17548138
Citation
Aseffa A, Bedru A, Yamuah L, Arga D, Worku A, Chandramohan D, Nelson CB, Engers HD. Safety of a trivalent meningococcal ACW135 vaccine among young children in Ethiopia. Vaccine. 2007 Sep 3;25 Suppl 1:A79-82. doi: 10.1016/j.vaccine.2007.04.046. Epub 2007 May 4.
Results Reference
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Safety, Immunogenicity and Reactogenicity Trial of Mencevax ACW135 Vaccine

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