A Phase 1/2b Study of an Investigational Malaria Vaccination Strategy in 5-17 Month Old Infants and Children in Burkina Faso

University of Oxford

Status and phase

Completed

Phase 2

Phase 1

Conditions

Malaria

Treatments

Biological: ChAd63 ME-TRAP and MVA ME-TRAP

Biological: Rabies vaccine

Study type

Interventional

Funder types

Other

Identifiers

NCT01635647

VAC050

Details and patient eligibility

About

Prime boost vaccination with ChAd63 ME-TRAP followed eight weeks later with MVA ME-TRAP shows efficacy against malaria infection when tested in UK volunteers using sporozoite challenge experiments. It is a leading candidate vaccination strategy against malaria. In the field, Phase I studies have been conducted in adults in Kenya and The Gambia and children and infants in The Gambia. The vaccination strategy appears safe and well tolerated in these populations, and also shows impressive immunogenicity, not significantly different to that seen in the UK trials where efficacy was shown. In particular, recent data from The Gambia shows excellent safety and immunogenicity in infants in malaria endemic areas, who would be the ones to benefit most from such a vaccine against malaria. With this clinical development as background, the investigators now propose to evaluate efficacy against natural malaria infection in this important target group for an effective malaria vaccine, that is, 5-17 month infants and children living in malaria endemic areas. The proposed study area, Banfora, Burkina Faso, is highly endemic for Plasmodium falciparum malaria.

Enrollment

730 patients

Sex

All

Ages

5 to 17 months old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy infant/child aged 5-17 months at the time of first study vaccination
Informed consent of parent/guardian
Infant / child and parent/guardian resident in the study area villages and anticipated to be available for vaccination and follow-up

Exclusion criteria

Clinically significant skin disorder (psoriasis, contact dermatitis etc.), immunodeficiency, cardiovascular disease, respiratory disease, endocrine disorder, liver disease, renal disease, gastrointestinal disease, neurological illness.
Weight-for-age Z score of less than -3 or other clinical signs of malnutrition
History of allergic reaction, significant IgE-mediated event, or anaphylaxis to immunisation
History of allergic disease or reactions likely to be exacerbated by any component of the vaccines, e.g. egg products, Kathon, neomycin, beta-propiolactone.
Haemoglobin less than 8.0 g/dL, where judged to be clinically significant in the opinion of the investigator
Serum Creatinine concentration greater than 70 µmol/L, where judged to be clinically significant in the opinion of the investigator
Serum ALT concentration greater than 45 U/L, where judged to be clinically significant in the opinion of the investigator
Blood transfusion within one month of enrolment
Previous vaccination with experimental malaria vaccines.
Administration of any other vaccine or immunoglobulin less than one week before vaccination with any study vaccine.
Current participation in another clinical trial, or within 12 weeks of this study.
Any other finding which in the opinion of the investigators would increase the risk of an adverse outcome from participation in the trial or result in incomplete or poor quality data
Known maternal HIV infection (No testing will be done by the study team)
Immunosuppressive therapy (steroids, immune modulators or immune suppressors) within 3 months prior recruitment. (For corticosteroids, this will mean prednisone, or equivalent, greater than or equal to 0.5 mg/kg/day. Inhaled and topical steroids are allowed.)