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Phase 3 Completed N=705 Randomized Prevention

Study to Evaluate Immunogenicity of the Hepatitis B Antigen of the GSK Biologicals' Candidate Malaria Vaccine (257049)

Malaria · Malaria Vaccines
Source: ClinicalTrials.gov NCT01345240 ↗
Enrolled (actual)
705
Serious AEs
4.8%
Results posted
Feb 2014
Primary outcomePrimary: Percentage of Seroprotected Subjects Against Anti-Hepatitis B (HBs) Antigen — 100; 96 Percentage of subjects

Summary

This study has been designed to support the indication of the candidate vaccine (also referred to as GSK 257049 or RTS,S in this record) against hepatitis B virus infection, when administered as a primary vaccination integrated into an Expanded Program on Immunization (EPI) regimen to infants living in sub-Saharan Africa.

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Seroprotected Subjects Against Anti-Hepatitis B (HBs) Antigen
100; 96
PRIMARY
Anti-Hepatitis B (HBs) Antibody Concentrations for RTS,S Group and Engerix B Group
6412.7; 377.4
PRIMARY
Anti-Hepatitis B (HBs) Antibody Concentrations for All Study Groups
5467.6; 6989.9; 6998.7; 334.4; 433.4
SECONDARY
Anti-Hepatitis B (HBs) Antibody Concentrations at Month 3
6214.3; 6826.1; 6209.2
SECONDARY
Anti-Hepatitis B (HBs) Antibody Concentrations at Month 14 and 26
1530.1; 2430.9; 2189.1; 119.5; 137.5; 1092.6
SECONDARY
Anti-Hepatitis B (HBs) Antibody Concentrations at Month 38, 50 and 51
706.8; 1081.7; 977.4; 39.0; 41.2; 499.4
SECONDARY
Concentrations of Antibodies to the Hepatitis B RF1 Surface Antigen (Anti-HBs RF1) at Month 3
268.7; 327.1; 335.5; 25.5; 28.7
SECONDARY
Concentrations of Antibodies to the Hepatitis B RF1 Surface Antigen (Anti-HBs RF1) at Month 51
307.8; 471.6; 514.5; 120.5; 127.9
SECONDARY
Anti-circumsporozoite Protein (Anti-CS) Antibody Concentrations at Month 3
142.2; 188.5; 205.5; 0.3; 0.3
SECONDARY
Anti-circumsporozoite Protein (Anti-CS) Antibody Concentrations at Month 14
5.7; 6.8; 7.5; 0.3; 0.3
SECONDARY
Anti-circumsporozoite Protein (Anti-CS) Antibody Concentrations at Month 38 and 50
2.6; 2.8; 3.5; 1.0; 1.0; 2.3
SECONDARY
Pneumococcal Antibody Concentrations Against Synflorix Pneumococcal Vaccine Serotypes at Month 3
3.1; 3.6; 3.5; 4.2; 5.1; 6.5
SECONDARY
Pneumococcal Antibody Concentrations Against Synflorix Pneumococcal Vaccine Serotypes at Month 17
4.5; 5.4; 6.1; 6.8; 6.5; 7.6
SECONDARY
Titers for Opsonophagocytic Activity Against Synflorix Pneumococcal Vaccine Serotypes at Month 3
48.9; 65.0; 768.3; 810.9; 77.6; 93.8
SECONDARY
Titers for Opsonophagocytic Activity Against Synflorix Pneumococcal Vaccine Serotypes at Month 17
649.9; 840.1; 2347.1; 2527.8; 324.2; 392.8
SECONDARY
Anti-protein D (PD) Antibody Concentrations at Month 3
2435.3; 2956.7
SECONDARY
Anti-protein D (PD) Antibody Concentrations at Month 17
2648.3; 2819.1
SECONDARY
Concentrations of Antibodies Against Acellular B-pertussis (BPT) at Day 0 and at Month 3
3.8; 4.3; 105.9; 114.2; 13.9; 15.7
SECONDARY
Anti-Rotavirus (Anti-RV) Antibody Concentrations
24.9; 27.6
SECONDARY
Number of Subjects With Solicited Local Symptoms
41; 28; 31; 29; 15; 30
SECONDARY
Number of Subjects With Solicited General Symptoms
44; 20; 16; 23; 13; 30
SECONDARY
Number of Subjects With Potential Immune Mediated Disorders (pIMDs) From Day 0 to Month 8
0; 0; 0; 0; 0
SECONDARY
Number of Subjects With Potential Immune Mediated Disorders (pIMDs) From Day 0 to Month 26
0; 0; 0; 0; 0
SECONDARY
Number of Subjects With Potential Immune Mediated Disorders (pIMDs) From Day 0 up to Study End (Month 51)
0; 0; 0; 0; 0
SECONDARY
Number of Subjects With Unsolicited Adverse Events (AEs)
121; 115; 120; 120; 105
SECONDARY
Number of Subjects With Any and Fatal Serious Adverse Events (SAEs) Within the 30-day Follow-up Periods (Days 0-29)
1; 3; 3; 1; 3; 1
SECONDARY
Number of Subjects With Any and Fatal Serious Adverse Events (SAEs) From Day 0 to Month 8
1; 7; 7; 3; 5; 1
SECONDARY
Number of Subjects With Any and Fatal Serious Adverse Events (SAEs) From Day 0 to Month 26
1; 8; 7; 6; 6; 1
SECONDARY
Number of Subjects With Any, Fatal and Related Serious Adverse Events (SAEs) From Day 0 up to Study End (Month 51)
3; 10; 9; 6; 6; 3

Eligibility Criteria

Inclusion Criteria

All subjects must satisfy ALL the following criteria at study entry:

  • A male or female infant aged between 8 and 12 weeks inclusive at the time of first vaccination
  • Signed or thumb-printed informed consent obtained from the parent(s)/Legally Acceptable Representative [LAR(s)] of the child. Where parent(s)/LAR(s) are illiterate, the consent form will be countersigned by an independent witness
  • Subjects who the investigator believes that their parent(s)/LAR(s) can and will comply with the requirements of the protocol
  • Healthy subjects 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
  • Born to a mother who is Human Immunodeficiency Virus (HIV) negative
  • Born after a normal gestation period of 36 to 42 weeks inclusive.

Exclusion Criteria

The following criteria should be checked at the time of study entry. If ANY exclusion criterion applies, the subject must not be included in the study:

  • Child in care
  • Acute disease and/or fever at the time of enrolment
  • Serious acute or chronic illness determined by clinical or physical examination and laboratory screening tests
  • Laboratory screening tests out of range
  • Previous vaccination with diphtheria, tetanus, pertussis, Haemophilus influenzae type b, Streptococcus pneumoniae, hepatitis B vaccine or rotavirus vaccines.
  • Planned administration/administration of a licensed vaccine not foreseen by the study protocol within 7 days of the first dose of study vaccine.
  • Use of a drug or vaccine that is not approved for that indication 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 in the period between birth and Dose 1 and within the three months preceding planned vaccine administration during the study period.
  • Chronic administration of immunosuppressants or other immune-modifying drugs in the period between birth and Dose 1.
  • Concurrently participating in another clinical study at any time during the study period, in which the subject has been or will be exposed to an investigational or a non-investigational product.
  • Same sex twin
  • Maternal death
  • History of allergic reactions or anaphylaxis to previous immunizations.
  • History of allergic disease or reactions likely to be exacerbated by any component of the vaccine.
  • Any other findings that the investigator feels would increase the risk of having an adverse outcome from participation in the trial.
  • Any other findings that the investigator feels would result in data collected being incomplete or of poor quality.
  • Previous participation in any other malaria vaccine trial.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01345240). 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. Informational only — not medical advice.

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