Immunogenicity and Safety Study of GSK Biologicals' Influenza Vaccine GSK2321138A When Administered in Children
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- GlaxoSmithKline
- Enrollment
- 3,027
- Locations
- 60
- Primary Endpoint
- Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against 4 Strains of Influenza Disease.
Study Overview
Brief Summary
This study is designed to assess the safety and immunogenicity of GlaxoSmithKline (GSK) Biologicals' investigational vaccine GSK2321138A in children aged 3 to 17 years, and to describe safety and immunogenicity of the GSK Biologicals' investigational vaccine GSK2321138A in children aged 6 to 35 months.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 6 Months to 17 Years (Child)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Subjects who the investigator believes that their parent(s)/Legally Acceptable Representative(s) (LAR) can and will comply with the requirements of the protocol.
- •For non US countries:
- •- Children, male or female, aged between 6 months and 17 years at the time of the first study vaccination.
- •Children, male or female, aged between 3 and 17 years at the time of the first study vaccination
- •Written informed consent obtained from the subject parent(s) or LAR(s) of the subject. Assent obtained from the subject when applicable.
- •Subjects in stable health as determined by investigator's clinical examination and assessment of subjects' medical history.
- •Written informed assent obtained from the subject if/as required by local regulations.
- •Female subjects of non-childbearing potential may be enrolled in the study.
- •Female subjects of childbearing potential may be enrolled in the study, if the subject:
- •- has practiced adequate contraception for 30 days prior to vaccination,
- •- and has a negative urine pregnancy test on the day of vaccination,
- •- and has agreed to continue adequate contraception during the entire treatment period and for 2 months after completion of the vaccination series
Exclusion Criteria
- •Use of any investigational or non-registered product other than the study vaccine within 30 days preceding the first dose of the study vaccine or planned use during the study period. Routine registered childhood vaccinations are permitted.
- •Planned administration of any vaccine 30 days prior and 30 days after any study vaccine administration.
- •Acute or chronic, clinically-significant pulmonary, cardiovascular, hepatic or renal functional abnormality, as determined by medical history and physical examination.
- •Prior receipt of any seasonal or pandemic influenza vaccine (registered or investigational) within 6 months preceding the first dose of study vaccine, or planned use during the study period.
- •Chronic administration of immunosuppressants or other immune-modifying drugs within three months prior to enrolment in this study or planned administration during the study period.
- •Administration of immunoglobulins and/or any blood products within the three months prior to the enrolment in this study, or planned during the study.
- •Any confirmed or suspected immunosuppressive or immunodeficient condition based on medical history and physical examination.
- •History of seizures or progressive neurological disease.
- •History of Guillain-Barré syndrome within 6 weeks of receipt of prior inactivated influenza virus vaccine.
- •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 .
- •History of hypersensitivity to a previous dose of influenza vaccine, history of any reaction or hypersensitivity likely to be exacerbated by any component of the vaccines
- •Acute disease and/or fever at the time of enrolment
- •Ongoing aspirin therapy
- •Pregnant or lactating female
- •Female planning to become pregnant or planning to discontinue contraceptive precautions.
- •Any other condition which, in the opinion of the investigator, prevents the subject from participating in the study
- •Child in Care.
Arms & Interventions
GSK2321138A 1 Group
Subjects aged 3-17 years received if primed, 1 dose of GSK2321138A at Day 0 and if unprimed, 2 doses of GSK2321138A at Day 0 and Day 28. The vaccine was administered intramuscularly into the deltoid for subjects aged 12 months or above or into the anterolateral region of the thigh for subjects below 12 month of age. The vaccine was administered in the non-dominant side of the body at Day 0 and in the opposite side at Day 28.
Intervention: Influenza vaccine GSK2321138A (Biological)
Fluarix Group
Subjects aged 3-17 years received if primed, 1 dose of Fluarix at Day 0 and if unprimed, 2 doses of Fluarix at Day 0 and Day 28. The vaccine was administered intramuscularly into the deltoid for subjects aged 12 months or above or into the anterolateral region of the thigh for subjects below 12 month of age. The vaccine was administered in the non-dominant side of the body at Day 0 and in the opposite side at Day 28.
Intervention: FluarixTM (Biological)
GSK2604409A Group
Subjects aged 3-17 years received if primed, 1 dose of GSK2604409A at Day 0 and if unprimed, 2 doses of GSK2604409A at Day 0 and Day 28. The vaccine was administered intramuscularly into the deltoid for subjects aged 12 months or above or into the anterolateral region of the thigh for subjects below 12 month of age. The vaccine was administered in the non-dominant side of the body at Day 0 and in the opposite side at Day 28.
Intervention: Influenza vaccine GSK2604409A (Biological)
GSK2321138A 2 Group
Subjects aged 6-35 months received if primed, 1 dose of GSK2321138A at Day 0 and if unprimed, 2 doses of GSK2321138A at Day 0 and Day 28. The vaccine was administered intramuscularly into the deltoid for subjects aged 12 months or above or into the anterolateral region of the thigh for subjects below 12 month of age. The vaccine was administered in the non-dominant side of the body at Day 0 and in the opposite side at Day 28.
Intervention: Influenza vaccine GSK2321138A (Biological)
Outcomes
Primary Outcomes
Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against 4 Strains of Influenza Disease.
Time Frame: At Day 0 [PRE] and at Day 28 (for primed subjects) and Day 56 (for unprimed subjects) [POST]
Titers are presented as geometric mean titers (GMTs). The reference cut-off value was 1:10. The 4 influenza strains assessed were the FLU A/California/7/09 (H1N1), FLU A/Victoria/210/09 (H3N2), FLU B/Brisbane/60/08 (Victoria) and FLU B/Brisbane/3/07 (Yamagata).
Number of Seroconverted Subjects Against 4 Strains of Influenza Disease.
Time Frame: At Day 28 (for primed subjects) and Day 56 (for unprimed subjects)
A seroconverted subject was defined as a vaccinated subject who had either a pre-vaccination titer \< 1:10 and a post-vaccination titer ≥1:40, or a pre-vaccination titer ≥1:10 and at least a four-fold increase in post-vaccination titer. The 4 influenza strains assessed were the FLU A/California/7/09 (H1N1), FLU A/Victoria/210/09 (H3N2), FLU B/Brisbane/60/08 (Victoria) and FLU B/Brisbane/3/07 (Yamagata).
Secondary Outcomes
- Number of Seroprotected Subjects Against 4 Strains of Influenza.(At Day 0 [PRE] and at Day 28 (for primed subjects) and Day 56 (for unprimed subjects) [POST])
- Number of Subjects With Any and Grade 3 Solicited Local Symptoms.(During the 7-day (Days 0-6) follow-up period after any vaccination.)
- Number of Subjects With Any and Related Serious Adverse Events (SAEs).(During the entire study period (Day 0 - Day 180))
- Number of Days With Solicited Local Symptoms.(During the 7-day (Days 0-6) follow-up period after vaccination.)
- Number of Seroprotected Subjects Against 4 Strains of Influenza Disease(At Day 0 [PRE] and at Day 28 (for primed subjects) and Day 56 (for unprimed subjects) [POST])
- Mean Geometric Increase (MGI) Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against 4 Strains of Influenza Disease.(At Day 28 (for primed subjects) and Day 56 (for unprimed subjects))
- Number of Subjects With Any, Grade 3 and Related Medically Attended Adverse Events (MAEs).(During the entire study period (Day 0 - Day 180))
- Number of Seroprotected Subjects Against 4 Strains of Influenza Disease.(At Day 0 [PRE] and at Day 28 (for primed subjects) and Day 56 (for unprimed subjects) [POST])
- Number of Subjects With Any, Grade 3 and Related Solicited General Symptoms in Subjects Younger Than 6 Years Old.(During the 7-day (Days 0-6) follow-up period after any vaccination.)
- Number of Subjects With Any, Grade 3 and Related Solicited General Symptoms in Subjects Aged 6 Years or Older.(During the 7-day (Days 0-6) follow-up period after any vaccination.)
- Number of Subjects With Any, Grade 3 and Related Unsolicited Adverse Events (AEs).(During the 28-day (Days 0-27) follow-up period after any vaccination.)
- Number of Subjects With Any and Related Potential Immune-Mediated Diseases (pIMDs).(During the entire study period (Day 0 - Day 180))
- Number of Days With Solicited General Symptoms(During the 7-day (Days 0-6) follow-up period after vaccination.)
- Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against 4 Strains of Influenza Disease by Age Strata.(At Day 0 [PRE] and at Day 28 (for primed subjects) and Day 56 (for unprimed subjects) [POST])
- Number of Seroconverted Subjects Against 4 Strains of Influenza Disease by Age Strata.(At Day 28 (for primed subjects) and Day 56 (for unprimed subjects))
- Number of Seroprotected Subjects Against 4 Strains of Influenza Disease by Age Strata.(At Day 0 [PRE] and at Day 28 (for primed subjects) and Day 56 (for unprimed subjects) [POST])
- Mean Geometric Increase (MGI) Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against 4 Strains of Influenza Disease by Age Strata.(At Day 28 (for primed subjects) and Day 56 (for unprimed subjects))