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Phase 2 N=214 Randomized Triple-blind Prevention

Examine Safety and Immune Responses of GSK 257049 Vaccine When Administered to Infants Living in a Malaria-endemic Region

Malaria

Enrolled (actual)
214
Serious AEs
32.2%
Results posted
Jan 2013
Primary outcome: Primary: Number of Subjects With Serious Adverse Events (SAEs). — 17; 17 subjects

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
RTS,S/AS02D (Biological); TETRActHib™ (Biological); Engerix-B® (Biological)
Age
Pediatric · 0+ yrs
Sex
All
Sponsor
GlaxoSmithKline
Primary completion
Dec 2007

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Subjects With Serious Adverse Events (SAEs).
35; 34
SECONDARY
Number of Subjects With Serious Adverse Events (SAEs).
35; 34
SECONDARY
Concentrations of Antibodies Against Hepatitis B (Anti-HB)
14.0; 16.6; 10081.6; 392.4
SECONDARY
Concentrations of Anti-circumsporozoite Protein (Anti-CS) Antibodies.
0.4; 0.4; 199.9; 0.3; 58.8; 0.4
SECONDARY
Concentrations of Antibodies Against Anti-diphtheria (Anti-D)
1.4; 1.4
SECONDARY
Concentrations of Antibodies Against Tetanus (Anti-T)
6.2; 5.1
SECONDARY
Concentrations of Anti-Bordetella Pertussis Toxin Antibodies (Anti-BPT).
104.4; 106.8
SECONDARY
Concentrations of Anti-polyribosyl Ribitol Phosphate Antibodies (Anti-PRP).
22.1; 17.9
SECONDARY
Time to First Malaria Infection
1.01; 2.67
SECONDARY
Number of Subjects Prevalent for Plasmodium Falciparum (P. Falciparum)
4; 7
SECONDARY
Plasmodium Falciparum (P. Falciparum) Parasite Density in Subjects Prevalent for Parasitemia
11573; 10612
SECONDARY
Number of Subjects With Solicited Local Symptoms.
105; 105; 26; 23
SECONDARY
Number of Subjects With Solicited Local Symptoms.
105; 105; 26; 23
SECONDARY
Number of Subjects With Solicited General Symptoms.
60; 69; 25; 23; 81; 81
SECONDARY
Number of Subjects With Solicited General Symptoms.
60; 69; 25; 23; 81; 81
SECONDARY
Number of Subjects With Unsolicited Adverse Events (AEs).
32; 39
SECONDARY
Number of Subjects With Unsolicited Adverse Events (AEs).
32; 39
SECONDARY
Number of Subjects With Unsolicited Adverse Events (AEs).
32; 39

Summary

GSK Biologicals is developing in partnership with the Program for Appropriate Technology in Health (PATH) Malaria Vaccine Initiative a candidate malaria vaccine for the routine immunization of infants and children living in malaria endemic areas. The vaccine would offer protection against malaria disease due to the parasite Plasmodium falciparum. The vaccine would also provide protection against infection with hepatitis B virus (HBV). This trial is being carried out following the demonstration of efficacy of a previous version of the malaria candidate vaccine in children in Mozambique: there, the vaccine demonstrated approximately 30% efficacy against clinical episodes of malaria and approximately 58% efficacy against severe malaria disease. In order to integrate the malaria vaccine into the Expanded Program on Immunization (EPI) regimen, in malaria-endemic regions, for this trial, a 0.5 ml dose of GSK 257049 vaccine has been developed. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.

Eligibility Criteria

Inclusion Criteria

  • A male or female infant of between 6 and 12 weeks of age at the time of first vaccination.
  • Written informed consent obtained from the parent(s) or guardian(s) of the subject
  • Free of obvious health problems as established by medical history and clinical examination before entering into the study.
  • Born to a mother who is hepatitis B surface antigen (HBsAg) negative and human immunodeficiency virus (HIV) negative.
  • Born after a normal gestation period (between 36 and 42 weeks).
  • Subjects who the investigator believes that their parents/guardians can and will comply with the requirements of the protocol should be enrolled in the study.

Exclusion Criteria

  • Bacillus Calmette-Guérin tuberculosis vaccine (BCG) administration within one week of proposed administration of a study vaccine.
  • 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 immunoglobulins and/or any blood products since birth or planned administration during the study period.
  • Chronic administration (defined as more than 14 days) of immunosuppressants or other immune-modifying drugs since birth
  • Any chronic drug therapy to be continued during the study period.
  • Previous vaccination with diphtheria, tetanus, pertussis, Haemophilus influenzae type b or hepatitis B vaccines.
  • Major congenital abnormality.
  • Serious acute or chronic illness determined by clinical, physical examination and laboratory screening tests
  • Any medically diagnosed or suspected immunodeficient condition based on medical history and physical examination
  • A family history of congenital or hereditary immunodeficiency.
  • History of allergic disease or reactions likely to be exacerbated by any component of the vaccine.
  • History of any neurological disorders or seizures.
  • Maternal death.
  • Hemoglobin < 80 g/L
  • Simultaneous participation in any other clinical trial.
  • Same sex twin
  • Any other findings that the investigator feels would increase the risk of having an adverse outcome from participation in the trialModerate malnutrition at screening
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00197028). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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