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OpenTrials
Completed

NCT Number: NCT00982579

Safety and Immunogenicity Study of Candidate HIV-1 Vaccine Given to Healthy Infants Born to HIV-1/2-uninfected Mothers

Objectives:

Safety and immunogenicity of MVA.HIVA vaccine in 20-week-old healthy Gambian infants born to HIV-1/2-uninfected mothers.

Gross impact of MVA.HIVA on the immunogenicity of EPI vaccines (DTwPHib, HepB, PCV-7 and OPV) when administered at 20 weeks (4 weeks after the last EPI vaccines), who have had BCG vaccine within the first 4 weeks of life.

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Key information

Age range

Up to 3 day

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Medical Research Council Laboratories, The Gambia

Banjul, Fajara, The Gambia

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy infants, 19 weeks of age, with weight for age z-scores within 2 standard deviations of normal.
  • Have received all standard EPI immunizations according to national immunization programme.
  • Written informed consent by parent.
  • Mother HIV-1/2-uninfected.

Exclusion criteria

  • Acute disease at the time of vaccination (acute disease is defined as the presence of a moderate or severe illness with or without fever). All vaccines can be administered to persons with a minor illness such as diarrhoea, mild upper respiratory tract infection with or without low-grade febrile illness, i.e. axillary temperature of <37.5 °C ).
  • Axillary temperature of ≥ 37.5 °C at the time of vaccination.
  • Any clinically significant abnormal finding on screening from biochemistry or haematology at 19 weeks.
  • History of allergic disease or reactions likely to be exacerbated by any component of the vaccine, e.g. egg products.
  • Presence of any underlying disease that compromises the diagnosis and evaluation of response to the vaccine.
  • Invasive bacterial infections (pneumonia, meningitis).
  • Any other on-going chronic illness requiring hospital specialist supervision.
  • Administration of immunoglobulins and/or any blood products within one month preceding the planned administration of the vaccine candidate.
  • Any history of anaphylaxis in reaction to vaccination.
  • Research physician's assessment of lack of willingness by parents to participate and comply with all requirements of the protocol, or identification of any factor felt to significantly increase the infant's risk of suffering an adverse outcome.
  • Likelihood of travel away from the study area.
  • Untreated malaria infection.
  • Any other clinical evidence of infection.

Treatment and study plan

MVA.HIVA

Biological

1 dose of 5 x 10^7 pfu of MVA.HIVA administered intramuscularly

Primary outcomes

  1. For safety and reactogenicity: Actively and passively collected data on adverse events

    Time frame: Up to 16 weeks after vaccination

Secondary outcomes

  1. For immunity to EPI vaccines: Antibody levels to specific vaccines.

    Time frame: 1 week before and 1 week after vaccination

  2. For immunogenicity: Frequency of IFN-γ producing cells determined in ex-vivo (effector) and 10-day cultured (memory) ELISPOT assays after overnight stimulation with pools of HIVA-derived peptides

    Time frame: Up to 16 weeks after vaccination

Sponsors and collaborators

Lead sponsor

Medical Research Council

Other Gov

Collaborators

  • European and Developing Countries Clinical Trials Partnership (EDCTP)

Registry information

Official study title

An Open Randomized Phase I Study Evaluating Safety and Immunogenicity of a Candidate HIV-1 Vaccine, MVA.HIVA, Administered to Healthy Infants Born to HIV-1/2-uninfected Mothers

Acronym: PedVacc001

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Sep 23, 2009
Registry last updated
Feb 3, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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