Phase 3
N=230
Primary Vaccination Study With a Pneumococcal Conjugate Vaccine in Healthy Children 6 to 8 Weeks of Age
Infections, Rotavirus
Bottom Line
View on ClinicalTrials.gov: NCT00533507 ↗Enrolled (actual)
230
Serious AEs
—
Results posted
Jul 2009
Primary outcome: Primary: Concentration of Anti-Protein D Antibodies — 2277.6 EL.U/mL
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- Synflorix (Biological); Infanrix hexa (Biological); Rotarix (Biological)
- Age
- Pediatric · 0+ yrs
- Sex
- All
- Sponsor
- GlaxoSmithKline
- Primary completion
- Jun 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Concentration of Anti-Protein D Antibodies |
2277.6 | — |
| PRIMARY Concentration of Anti-Pneumococcal Antibodies |
2.92; 3.79; 4.50; 1.69; 4.07; 3.90 | — |
| SECONDARY Number of Subjects With Anti-Protein D Antibody Concentrations Above the Cut-Off Value |
38; 218 | — |
| SECONDARY Number of Subjects With Vaccine Pneumococcal Serotype Antibody Concentrations Above the Cut-Off Value |
111; 219; 85; 219; 149; 219 | — |
| SECONDARY Number of Subjects With Cross-Reactive Pneumococcal Serotype Antibody Concentrations Above the Cut-Off Value |
210; 200 | — |
| SECONDARY Number of Subjects With Opsonophagocytic Activity Against Vaccine Pneumococcal Serotypes Above the Cut-Off Value |
98; 103; 101; 89; 103; 98 | — |
| SECONDARY Number of Subjects With Opsonophagocytic Activity Against Cross-Reactive Pneumococcal Serotypes Above the Cut-Off Value |
87; 38 | — |
| SECONDARY Number of Subjects With Anti-Polyribosyl-Ribitol Phosphate Antibody Concentrations Above the Cut-Off Value |
58 | — |
| SECONDARY Number of Subjects With Anti-Diphteria and Anti-Tetanus Toxoids Antibody Concentrations Above the Cut-Off Value |
58; 58 | — |
| SECONDARY Number of Subjects With Anti-Pertussis (PT), Anti-Filamentous Hemagglutinin (FHA) and Anti-Pertactin (PRN) Antibody Concentrations Above the Cut-Off Value |
58; 58; 57 | — |
| SECONDARY Number of Subjects With Anti-Hepatitis B Surface Antigen (HBs) Antibody Concentrations Above the Cut-Off Value |
32 | — |
| SECONDARY Number of Subjects With Anti-Poliovirus 1, 2 and 3 Antibody Titers Above the Cut-Off Value |
44; 44; 44 | — |
| SECONDARY Number of Subjects With Anti-rotavirus Immunoglobulin A Antibody Concentrations Above the Cut-Off Value |
44 | — |
| SECONDARY Number of Subjects Reporting Solicited Symptoms |
146; 144; 139; 7; 190; 153 | — |
| SECONDARY Number of Subjects Reporting Unsolicited Adverse Events (AE) |
95 | — |
| SECONDARY Number of Subjects Reporting Serious Adverse Events (SAE) |
15 | — |
Summary
The purpose of this study is to assess the immunogenicity in terms of antibody response and the safety/reactogenicity in terms of solicited and unsolicited symptoms and serious adverse events following primary vaccination of Taiwanese infants with pneumococcal conjugate vaccine GSK 1024850A co-administered with a diphtheria, tetanus, acellular pertussis (DTPa)-combined vaccine and rotavirus vaccine in children during the first 6 months of life.
Eligibility Criteria
Inclusion Criteria
- Male or female subjects between, and including 6-8 weeks of age at the time of the first vaccination.
- Subjects for whom the investigator believes that their parent(s)/guardian(s) can and will comply with the requirements of the protocol.
- 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 after a gestation period of 36 to 42 weeks inclusive.
Exclusion Criteria
- Use of any investigational or non-registered product (drug or vaccine) other than the study vaccines within 30 days preceding the first dose of the study vaccines, or planned use during the study period.
- Planned administration/ administration of a vaccine not foreseen by the study protocol during the period starting one month before each dose of vaccines and ending 7 days after dose 1 and dose 2 and one month after dose 3.
- 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.
- Chronic administration (defined as more than 14 days) of immunosuppressants or other immune-modifying drugs since birth.
- A family history of congenital or hereditary immunodeficiency.
- Any confirmed or suspected immunosuppressive or immunodeficient condition based on medical history and physical examination.
- Administration of immunoglobulins and/or any blood products since birth or planned administration during the study period.
- Previous vaccination against diphtheria, tetanus, pertussis, polio, hepatitis B, Haemophilus influenzae type b, rotavirus and/or Streptococcus pneumoniae; with the exception of vaccines where the first dose may be given within the first two weeks of life according to the national recommendations (e.g. Hepatitis B and Bacillus Calmette-Guérin (BCG)).
- History of, or intercurrent, diphtheria, tetanus, pertussis, polio, hepatitis B and Haemophilus influenzae type b disease.
- Gastroenteritis within 7 days preceding the study vaccine administration (warrants deferral of the vaccination).
- Any clinically significant history of chronic gastrointestinal disease including any uncorrected congenital malformation of the gastrointestinal (GI) tract, intussusception (IS) or other medical condition determined to be serious by the investigator.
- History of allergic disease or reactions likely to be exacerbated by any component of the vaccines.
- History of any neurological disorders or seizures.
- Major congenital defects or serious chronic illness.
- Acute disease at the time of enrolment.
Data sourced from ClinicalTrials.gov (NCT00533507). 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.