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Clinical Trials/NCT01364883
NCT01364883
Completed
Phase 1

A Phase I Study to Assess the Safety and Immunogenicity of Novel Schedules for Vaccination With the Candidate Malaria Vaccines AdCh63 ME-TRAP and MVA ME-TRAP

University of Oxford1 site in 1 country39 target enrollmentJuly 2011
ConditionsMalaria

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Malaria
Sponsor
University of Oxford
Enrollment
39
Locations
1
Primary Endpoint
Vaccine Safety
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

This is an open label phase I study, to assess the safety and immunogenicity of novel schedules for vaccination with the candidate malaria vaccines AdCh63 ME-TRAP and MVA ME-TRAP. These vaccines have been evaluated previously in a number of clinical trials proved to be safe and capable of inducing protective cellular immune response following challenge with the parasite. All volunteers recruited will be healthy adults. They will be primed with AdCh63 ME-TRAP administered intramuscularly and boosted several times with AdCh63 ME-TRAP and MVA ME-TRAP according to various schedules.. Safety data will be collected for each of the seven regimens. Secondary aims of this study will be to assess the immune responses generated by each of these regimes.

Registry
clinicaltrials.gov
Start Date
July 2011
End Date
July 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy adults aged 18 to 50 years
  • Able and willing (in the Investigator's opinion) to comply with all study requirements
  • Willing to allow the investigators to discuss their medical history with their General Practitioner
  • For female volunteers, willingness to practice continuous effective contraception during the study
  • Agreement to refrain from blood donation during the course of the study
  • Written informed consent

Exclusion Criteria

  • Participation in another research study involving an investigational product in the 30 days preceding enrolment, or planned use during the study period
  • Prior receipt of an investigational malaria vaccine or any other investigational vaccine likely to impact on interpretation of the trial data
  • Administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate
  • Any confirmed or suspected immunosuppressive or immunodeficient state, including HIV infection; asplenia; recurrent, severe infections and chronic (more than 14 days) immunosuppressant medication within the past 6 months (inhaled and topical steroids are allowed)
  • Pregnancy, lactation, or intention to become pregnant during the study
  • History of allergic disease or reactions likely to be exacerbated by any component of the vaccine, e.g. egg products, Kathon History of clinically significant contact dermatitis
  • Any history of anaphylaxis in relation to vaccination
  • Any history of malaria Travel to a malaria endemic region during the study period or within the six months preceding enrolment in the study
  • History of serious psychiatric condition that may affect participation in the study
  • Any other serious chronic illness requiring hospital specialist supervision -Suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week

Outcomes

Primary Outcomes

Vaccine Safety

Time Frame: Participants will be followed for the duration of the study, an expected average of 21 months

To assess the safety of vaccination of healthy adults with AdCh63 ME-TRAP and MVA ME-TRAP according to vaccination schedules 1 to 7

Secondary Outcomes

  • Vaccine immunogenicity(Participants will be followed for the duration of the study, an expected average of 21months)

Study Sites (1)

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