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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT01051661
Registration number
NCT01051661
Ethics application status
Date submitted
14/01/2010
Date registered
18/01/2010
Titles & IDs
Public title
Safety and Efficacy of H1N1 Vaccines in Children Aged 6 Months to Less Than 10 Years of Age
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Scientific title
A Study to Evaluate the Safety and Efficacy of A/California/7/2009 (H1N1)V-like Vaccines GSK2340274A and GSK2340273A in Children Aged 6 Months to Less Than 10 Years of Age
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Secondary ID [1]
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0
114000
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Influenza
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0
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Condition category
Condition code
Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Other - GSK Biologicals' investigational vaccine GSK2340274A (alternative formulations)
Treatment: Other - GSK Biologicals' investigational vaccine GSK2340273A (alternative formulations)
Treatment: Other - Placebo
Experimental: Arepanrix 2D 6M-3Y Group - Subjects, male and female, aged 6 months (M) to 3 years (Y), received 2 doses (D) of the Arepanrix™ vaccine at a 21-day interval (Days 0 and 21). First doses were administered in the deltoid region of the non-dominant arm (or left arm if dominance is not yet identified) or, for children \<12 months of age, in the left anterolateral thigh. Second doses were administered at a 21-day interval in the deltoid region of the dominant arm (or right arm) or, for, children \<12 months of age, in the right anterolateral thigh.
Experimental: Arepanrix 2D 3Y-10Y Group - Subjects, male and female, aged 3 years (Y) to 10 years, received 2 doses (D) of the Arepanrix™ vaccine at a 21-day interval (Days 0 and 21). First doses were administered in the deltoid region of the non-dominant arm (or left arm if dominance is not yet identified). Second doses were administered at a 21-day interval in the deltoid region of the dominant arm (or right arm).
Experimental: Arepanrix 1D 6M-3Y Group - Subjects, male and female, aged 6 months (M) to 3 years (Y), received 1 dose (D) of the Arepanrix™ vaccine followed by 1 dose of saline placebo at a 21-day interval at a 21-day interval (Days 0 and 21). First doses were administered in the deltoid region of the non-dominant arm (or left arm if dominance is not yet identified) or, for children \<12 months of age, in the left anterolateral thigh. Second doses were administered at a 21-day interval in the deltoid region of the dominant arm (or right arm) or, for, children \<12 months of age, in the right anterolateral thigh.
Experimental: Arepanrix 1D 3Y-10Y Group - Subjects, male and female, aged 3 years (Y) to 10 years, received 1 dose (D) of the Arepanrix™ vaccine followed by 1 dose of saline placebo at a 21-day interval at a 21-day interval (Days 0 and 21). First doses were administered in the deltoid region of the non-dominant arm (or left arm if dominance is not yet identified). Second doses were administered at a 21-day interval in the deltoid region of the dominant arm (or right arm).
Experimental: GSK2340273A 6M-3Y Group - Subjects, male and female, aged 6 months (M) to 3 years (Y), received 2 doses (D) of the GSK2340273A vaccine at a 21-day interval (Days 0 and 21). First doses were administered in the deltoid region of the non-dominant arm (or left arm if dominance is not yet identified) or, for children \<12 months of age, in the left anterolateral thigh. Second doses were administered at a 21-day interval in the deltoid region of the dominant arm (or right arm) or, for, children \<12 months of age, in the right anterolateral thigh.
Experimental: GSK2340273A 3Y-10Y Group - Subjects, male and female, aged 3 years (Y) to 10 years, received 2 doses (D) of the GSK2340273A vaccine at a 21-day interval (Days 0 and 21). First doses were administered in the deltoid region of the non-dominant arm (or left arm if dominance is not yet identified). Second doses were administered at a 21-day interval in the deltoid region of the dominant arm (or right arm).
Treatment: Other: GSK Biologicals' investigational vaccine GSK2340274A (alternative formulations)
Intramuscular injection, one or two doses
Treatment: Other: GSK Biologicals' investigational vaccine GSK2340273A (alternative formulations)
Intramuscular injection, two doses
Treatment: Other: Placebo
Intramuscular injection, one dose
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Intervention code [1]
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Treatment: Other
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Number of Subjects Reporting at Least One A/California Influenza Event
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Assessment method [1]
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The influenza virus presence was confirmed by quantitative reverse transcription polymerase chain reaction assay (RT-qPCR).
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Timepoint [1]
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From 14 days after first vaccination until study conclusion on Day 385
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Secondary outcome [1]
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Number of Subjects Reporting at Least One A/California Influenza Event
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Assessment method [1]
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The influenza virus presence was confirmed by quantitative reverse transcription polymerase chain reaction assay (RT-qPCR).
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Timepoint [1]
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From 42 days after first vaccination until study conclusion on Day 385
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Secondary outcome [2]
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Number of Subjects Reporting at Least One A/California Influenza Event
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Assessment method [2]
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The influenza virus presence was confirmed by quantitative reverse transcription polymerase chain reaction assay (RT-qPCR).
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Timepoint [2]
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From Day 0 until study conclusion on Day 385
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Secondary outcome [3]
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Number of Subjects Reporting at Least One Culture Confirmed A/California Influenza Event
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Assessment method [3]
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The influenza virus presence was confirmed by a positive culture.
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Timepoint [3]
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From 14 days after first vaccination until study conclusion on Day 385
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Secondary outcome [4]
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Number of Subjects Reporting at Least One Culture Confirmed A/California Influenza Event
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Assessment method [4]
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The influenza virus presence was confirmed by a positive culture.
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Timepoint [4]
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From 42 days after first vaccination until study conclusion on Day 385
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Secondary outcome [5]
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Number of Subjects Reporting at Least One Culture Confirmed A/California Influenza Event
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Assessment method [5]
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The influenza virus presence was confirmed by a positive culture.
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Timepoint [5]
0
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From Day 0 until study conclusion on Day 385
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Secondary outcome [6]
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Number of Subjects With at Least One Pneumonia Event
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Assessment method [6]
0
0
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Timepoint [6]
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From 14 days after first vaccination until study conclusion on Day 385
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Secondary outcome [7]
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Number of Subjects With at Least One Pneumonia Event
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Assessment method [7]
0
0
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Timepoint [7]
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From 42 days after first vaccination until study conclusion on Day 385
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Secondary outcome [8]
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0
Number of Subjects With at Least One Pneumonia Event
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Assessment method [8]
0
0
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Timepoint [8]
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From Day 0 after first vaccination until study conclusion on Day 385
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Secondary outcome [9]
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Number of Subjects With at Least One Pneumonia Event
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Assessment method [9]
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Pneumonia was confirmed by quantitative reverse transcription polymerase chain reaction assay (RT-qPCR).
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Timepoint [9]
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From 14 days after first vaccination until study conclusion at Day 385
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Secondary outcome [10]
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Number of Subjects With at Least One Pneumonia Event
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Assessment method [10]
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Pneumonia was confirmed by quantitative reverse transcription polymerase chain reaction assay (RT-qPCR).
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Timepoint [10]
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From 42 days after first vaccination until study conclusion at Day 385
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Secondary outcome [11]
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Number of Subjects With at Least One Pneumonia Event
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Assessment method [11]
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Pneumonia was confirmed by quantitative reverse transcription polymerase chain reaction assay (RT-qPCR).
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Timepoint [11]
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From Day 0 after first vaccination until study conclusion at Day 385
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Secondary outcome [12]
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Number of Subjects With Protocol Specified Influenza-like Illness (ILI) Symptoms in All Reported ILI Cases
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Assessment method [12]
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Protocol specified ILI symptoms were: fever, muscle aches all over the body, cough, sore throat, runny or stuffy nose, short of breath, headache, vomiting, diarrhea, chills and fatigue.
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Timepoint [12]
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From Day 0 until study end at Day 385
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Secondary outcome [13]
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Number of Subjects With Protocol Specified Influenza-like Illness (ILI) Symptoms in All Reported ILI Cases
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Assessment method [13]
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Protocol specified ILI symptoms were: fever, muscle aches all over the body, cough, sore throat, runny or stuffy nose, short of breath, headache, vomiting, diarrhea, chills and fatigue. Analysis for the time frame Day 42 till Day 385 was not performed as planned per protocol.
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Timepoint [13]
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From Day 14 until study end at Day 385
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Secondary outcome [14]
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Number of Subjects With Protocol Specified ILI Symptoms in RT-qPCR-confirmed A/California Influenza Cases
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Assessment method [14]
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Protocol specified ILI symptoms were: fever, muscle aches all over the body, cough, sore throat, runny or stuffy nose, short of breath, headache, vomiting, diarrhea, chills and fatigue.
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Timepoint [14]
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From Day 0 until study end at Day 385
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Secondary outcome [15]
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Number of Subjects With Protocol Specified ILI Symptoms in RT-qPCR-confirmed A/California Influenza Cases
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Assessment method [15]
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Protocol specified ILI symptoms were: fever, muscle aches all over the body, cough, sore throat, runny or stuffy nose, short of breath, headache, vomiting, diarrhea, chills and fatigue. Analysis for the time frame Day 42 till Day 385 was not performed as planned per protocol.
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Timepoint [15]
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From Day 14 until study end at Day 385
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Secondary outcome [16]
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Number of Subjects With Any and Grade 3 Solicited Local Symptoms
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Assessment method [16]
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Assessed solicited local symptoms were pain, redness and swelling. Any = occurrence of the symptom regardless of intensity grade. Grade 3 pain = pain that prevented normal activity. Grade 3 redness/swelling = redness/swelling spreading beyond 100 millimeters (mm) of injection site.
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Timepoint [16]
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During the 7-day follow-up period (Day 0 - Day 6) after each dose and across doses
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Secondary outcome [17]
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Number of Subjects With Any, Grade 3 and Related Solicited General Symptoms in Children Aged 6 Months to Less Than 6 Years
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Assessment method [17]
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Assessed solicited general symptoms were drowsiness, irritability, loss of appetite and temperature \[defined as axillary temperature equal to or above (=) 38.0 degrees Celsius (°C)\]. Any = occurrence of the symptom regardless of intensity grade. Grade 3 drowsiness = drowsiness which prevented normal everyday activity. Grade 3 irritability = crying that could not be comforted/ prevented normal activity. Grade 3 loss of appetite = not eating at all. Grade 3 temperature = fever = 39.0 °C. Related = symptom assessed by the investigator as related to the vaccination.
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Timepoint [17]
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During the 7-day follow-up period (Day 0 - Day 6) after each dose and across doses
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Secondary outcome [18]
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Number of Subjects With Any, Grade 3 and Related Solicited General Symptoms in Children Aged Between 6 to 10 Years
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Assessment method [18]
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Assessed solicited general symptoms were fatigue, gastrointestinal symptoms (gastro.sympt.), headache, joint pain at other location, muscle aches, shivering, sweating and temperature \[defined as axillary temperature equal to or above (=) 38.0 degrees Celsius (°C)\]. Any = Incidence of a particular symptom regardless of intensity grade or relationship to study vaccination. Grade 3 = symptom which prevented normal everyday activity. Grade 3 temperature = fever = 39.0 °C. Related = symptom assessed by the investigator as related to the vaccination.
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Timepoint [18]
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0
During the 7-day follow-up period (Day 0 - Day 6) after each dose and across doses
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Secondary outcome [19]
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Number of Subjects Reporting Any Potential Immune-mediated Diseases (pIMDs)
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Assessment method [19]
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Potential immune-mediated diseases (pIMDs) are a subset of AEs that include autoimmune diseases and other inflammatory and/or neurologic disorders of interest which may or may not have an autoimmune aetiology.
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Timepoint [19]
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Up to Day 385
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Secondary outcome [20]
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Number of Subjects With Any Medically-attended Adverse Events (MAEs)
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Assessment method [20]
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MAEs were defined as events for which the subject received medical attention defined as hospitalization, an emergency room visit, or a visit to or from medical personnel (medical doctor) for any reason. Any MAE(s) = Occurrence of any MAE(s) regardless of intensity grade or relation to vaccination.
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Timepoint [20]
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Up to Day 385
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Secondary outcome [21]
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Number of Subjects With Any Unsolicited Adverse Events (AEs)
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Assessment method [21]
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An unsolicited AE covers any untoward medical occurrence in a clinical investigation subject temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product and reported in addition to those solicited during the clinical study and any solicited symptom with onset outside the specified period of follow-up for solicited symptoms. Any was defined as the occurrence of any unsolicited AE regardless of intensity grade or relation to vaccination.
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Timepoint [21]
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From Day 0 to Day 42
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Secondary outcome [22]
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Number of Subjects With Serious Adverse Events (SAEs)
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Assessment method [22]
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Serious adverse events (SAEs) assessed include medical occurrences that result in death, are life threatening, require hospitalization or prolongation of hospitalization or result in disability/incapacity.
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Timepoint [22]
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Up to Day 385
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Secondary outcome [23]
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Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [23]
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Titers are presented as geometric mean titers (GMTs).
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Timepoint [23]
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At Days 0 and 42
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Secondary outcome [24]
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Number of Seropositive Subjects for Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [24]
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A seropositive subject was defined as a subject whose HI titers were greater than or equal to (=) 1:10.
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Timepoint [24]
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At Days 0 and 42
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Secondary outcome [25]
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Number of Seroconverted (SCR) Subjects for Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [25]
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Seroconversion was defined as: for initially seronegative subjects, antibody titer = 1:40 after vaccination; and for initially seropositive subjects, antibody titer after vaccination = 4 fold the pre-vaccination antibody titer.
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Timepoint [25]
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At Day 42
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Secondary outcome [26]
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Number of Seroprotected (SPR) Subjects Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [26]
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A seroprotected subject was defined as a vaccinated subject with serum Hemagglutination Inhibition (HI) titer = 1:40.
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Timepoint [26]
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At Days 0 and 42
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Secondary outcome [27]
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Seroconversion Factor for Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [27]
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The seroconversion factor (SCF) was defined as the fold increase in serum Hemagglutination Inhibition (HI) geometric mean titers (GMTs) post-vaccination compared to Day 0.
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Timepoint [27]
0
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At Day 42
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Secondary outcome [28]
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Geometric Mean Antibody Titer Ratio Adjusted for Baseline Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 (H1N1)
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Assessment method [28]
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The geometric mean titer ratio (GMT ratio) was defined as the ratio of geometric mean of the post-vaccination reciprocal HI titer between groups. The analysis was not performed for Day 182 and Day 385 as planned per protocol.
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Timepoint [28]
0
0
At Day 42
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Secondary outcome [29]
0
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Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 (H1N1)
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Assessment method [29]
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Titers are presented as geometric mean titers (GMTs).
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Timepoint [29]
0
0
At Days 0 and 182
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Secondary outcome [30]
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Number of Seropositive Subjects for Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [30]
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A seropositive subject was defined as a subject whose HI titers were greater than or equal to (=) 1:10.
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Timepoint [30]
0
0
At Days 0 and 182
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Secondary outcome [31]
0
0
Number of Seroconverted (SCR) Subjects for Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [31]
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Seroconversion was defined as: for initially seronegative subjects, antibody titer = 1:40 after vaccination; and for initially seropositive subjects, antibody titer after vaccination = 4 fold the pre-vaccination antibody titer.
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Timepoint [31]
0
0
At Day 182
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Secondary outcome [32]
0
0
Number of Seroprotected (SPR) Subjects Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [32]
0
0
A seroprotected subject was defined as a vaccinated subject with serum Hemagglutination Inhibition (HI) titer = 1:40.
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Timepoint [32]
0
0
At Days 0 and 182
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Secondary outcome [33]
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Seroconversion Factor for Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [33]
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The seroconversion factor (SCF) was defined as the fold increase in serum Hemagglutination Inhibition (HI) geometric mean titers (GMTs) post vaccination compared to Day 0.
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Timepoint [33]
0
0
At Day 182
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Secondary outcome [34]
0
0
Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [34]
0
0
Titers are presented as geometric mean titers (GMTs).
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Timepoint [34]
0
0
At Days 0 and 385
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Secondary outcome [35]
0
0
Number of Seropositive Subjects for Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [35]
0
0
A seropositive subject was defined as a subject whose HI titers was greater than or equal to (=) 1:10.
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Timepoint [35]
0
0
At Days 0 and 385
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Secondary outcome [36]
0
0
Number of Seroconverted (SCR) Subjects for Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [36]
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0
Seroconversion was defined as: for initially seronegative subjects, antibody titer = 1:40 after vaccination; and for initially seropositive subjects, antibody titer after vaccination = 4 fold the pre-vaccination antibody titer.
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Timepoint [36]
0
0
At Day 385
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Secondary outcome [37]
0
0
Number of Seroprotected (SPR) Subjects Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [37]
0
0
A seroprotected subject was defined as a vaccinated subject with serum Hemagglutination Inhibition (HI) titer = 1:40.
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Timepoint [37]
0
0
At Days 0 and 385
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Secondary outcome [38]
0
0
Seroconversion Factor for Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 (H1N1) Influenza Strain
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Assessment method [38]
0
0
The seroconversion factor (SCF) was defined as the fold increase in serum Hemagglutination Inhibition (HI) geometric mean titers (GMTs) post vaccination compared to Day 0.
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Timepoint [38]
0
0
At Day 385
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Eligibility
Key inclusion criteria
* Male or female children 6 months to less than 10 years of age at the time of the first vaccination. "Less than 10 years of age" implies inclusion of children who have not reached their 10th birthday as of Day 0, the day of first vaccine dose under this protocol.
* Written informed consent obtained from the subject's parent(s)/legally acceptable representative(s) (LAR(s)); written informed assent obtained from the subject if appropriate pre local requirements).
* Stable health status as defined by absence of a health event satisfying the definition of a SAE, or a change in an ongoing drug therapy due to therapeutic failure or symptoms of drug toxicity, within 1 month prior to enrolment.
* Parent(s)/LAR(s) available and accessible for active surveillance contacts.
* Parent(s)/LAR(s) and (if age-appropriate, subjects) who, in the investigator's opinion, can and will comply with the requirements of the protocol as documented by signature on the informed consent document.
* Female subjects of non-childbearing potential (pre-menarche) may be enrolled in the study.
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Minimum age
6
Months
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Maximum age
9
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
* Previous vaccination with an A/California/7/2009 (H1N1)v-like virus vaccine.
* Medical history of physician-confirmed infection with an A/California/7/2009 (H1N1)v-like virus.
* Presence of evidence of substance abuse or of neurological or psychiatric diagnoses which, even if stable, are deemed by the investigator to render the potential subject or parent(s)/LAR(s) unable/unlikely to provide accurate safety reports.
* Presence of a temperature = 38.0ºC (= 100.4ºF) by any route or method, or acute symptoms greater than "mild" severity on the scheduled date of first vaccination. NOTE: The subject may be vaccinated at a later date, provided symptoms have resolved, vaccination occurs within the window specified by the protocol, and all other eligibility criteria continue to be satisfied.
* Diagnosed with cancer, or treatment for cancer, within 3 years.
* Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination (no laboratory testing required).
* Receipt of systemic glucocorticoids within 1 month prior to study enrollment (first dose of study vaccine), or any other cytotoxic or immunosuppressive drug within 6 months of study enrollment. Topical, intra-articular or inhaled glucocorticoids are allowed.
* Receipt of any immunoglobulins and/or any blood products within 6 months of study enrollment or planned administration of any of these products during the study period.
* Any significant disorder of coagulation or treatment with warfarin derivatives or heparin. Persons receiving individual doses of low molecular weight heparin are eligible if no such doses are given in the 24 hours before a study vaccination. Persons receiving prophylactic antiplatelet medications, e.g., low-dose acetylsalicylic acid, and without a clinically-apparent bleeding tendency, are eligible.
* An acute evolving neurological disorder or history of Guillain-Barré syndrome within 6 weeks of receipt of seasonal influenza vaccine.
* Administration of any licensed live attenuated vaccine within 4 weeks before the first vaccination or of any licensed inactivated vaccine within 2 weeks before the first vaccination.
* Planned administration of any vaccine not foreseen by the study protocol between Day 0 and Day 42. Routine childhood vaccinations are exempted if they cannot be delayed, but they must not be administered on the same day as the H1N1 vaccine candidate.
* Planned use of a pandemic monovalent A/California/7/2009 (H1N1)v-like virus vaccine other than the study vaccines during the study period.
* Planned administration of seasonal trivalent influenza vaccine during the 4 month period following Day 0.
* Use of any investigational or non-registered product (drug or vaccine) other than the study vaccine(s) within 30 days before the first dose of study vaccine, or planned use during the study period.
* Any known or suspected allergy to any constituent of influenza vaccines (including egg proteins or mercurial preservatives); a history of anaphylactic-type reaction to consumption of eggs; or a history of severe adverse reaction to a previous influenza vaccine.
* Child in care.
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
12/02/2010
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
9/09/2011
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Sample size
Target
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Accrual to date
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Final
6154
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Recruitment in Australia
Recruitment state(s)
QLD,VIC
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Recruitment hospital [1]
0
0
GSK Investigational Site - Kippa Ring
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Recruitment hospital [2]
0
0
GSK Investigational Site - Carlton
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Recruitment postcode(s) [1]
0
0
4021 - Kippa Ring
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Recruitment postcode(s) [2]
0
0
3053 - Carlton
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Recruitment outside Australia
Country [1]
0
0
Brazil
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State/province [1]
0
0
Santa Catarina
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Country [2]
0
0
Brazil
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State/province [2]
0
0
São Paulo
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Country [3]
0
0
Colombia
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State/province [3]
0
0
Cali
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Country [4]
0
0
Costa Rica
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State/province [4]
0
0
San Jose
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Country [5]
0
0
Mexico
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State/province [5]
0
0
Morelos
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Country [6]
0
0
Mexico
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Durango
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Mexico
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Mexico city
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Mexico
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Monterrey
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Philippines
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Dasmariñas, Cavite
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Philippines
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Muntinlupa
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Philippines
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Sampaloc, Manila
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Singapore
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Singapore
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Thailand
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Bangkok
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Thailand
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Khon Kaen
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
GlaxoSmithKline
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Ethics approval
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Summary
Brief summary
The purpose of this study is to characterize the safety and efficacy of GSK Biologicals' H1N1 flu candidate vaccines GSK2340274A and GSK2340273A in children 6 months to less than 10 years of age.
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Trial website
https://clinicaltrials.gov/study/NCT01051661
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Trial related presentations / publications
Nolan T, Roy-Ghanta S, Montellano M, Weckx L, Ulloa-Gutierrez R, Lazcano-Ponce E, Kerdpanich A, Safadi MA, Cruz-Valdez A, Litao S, Lim FS, de Los Santos AM, Weber MA, Tinoco JC, Mezerville MH, Faingezicht I, Kosuwon P, Lopez P, Borja-Tabora C, Li P, Durviaux S, Fries L, Dubin G, Breuer T, Innis BL, Vaughn DW. Relative efficacy of AS03-adjuvanted pandemic influenza A(H1N1) vaccine in children: results of a controlled, randomized efficacy trial. J Infect Dis. 2014 Aug 15;210(4):545-57. doi: 10.1093/infdis/jiu173. Epub 2014 Mar 20. Taylor S, Lopez P, Weckx L, Borja-Tabora C, Ulloa-Gutierrez R, Lazcano-Ponce E, Kerdpanich A, Angel Rodriguez Weber M, Mascarenas de Los Santos A, Tinoco JC, Safadi MA, Lim FS, Hernandez-de Mezerville M, Faingezicht I, Cruz-Valdez A, Feng Y, Li P, Durviaux S, Haars G, Roy-Ghanta S, Vaughn DW, Nolan T. Respiratory viruses and influenza-like illness: Epidemiology and outcomes in children aged 6 months to 10 years in a multi-country population sample. J Infect. 2017 Jan;74(1):29-41. doi: 10.1016/j.jinf.2016.09.003. Epub 2016 Sep 22.
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Public notes
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Contacts
Principal investigator
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GSK Clinical Trials
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GlaxoSmithKline
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Contact person for scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
IPD for this study will be made available via the Clinical Study Data Request site.
Supporting document/s available: Study protocol, Statistical analysis plan (SAP), Informed consent form (ICF), Clinical study report (CSR)
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When will data be available (start and end dates)?
IPD is available via the Clinical Study Data Request site (click on the link provided below)
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Available to whom?
Access is provided after a research proposal is submitted and has received approval from the Independent Review Panel and after a Data Sharing Agreement is in place. Access is provided for an initial period of 12 months but an extension can be granted, when justified, for up to another 12 months.
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Available for what types of analyses?
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How or where can data be obtained?
IPD available at link: http://clinicalstudydatarequest.com
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results are available at
https://clinicaltrials.gov/study/NCT01051661