Diese Seite wurde automatisch übersetzt und die Genauigkeit der Übersetzung wird nicht garantiert. Bitte wende dich an die englische Version für einen Quelltext.

Immunogenicity and Safety Study of FluarixTM Vaccine in Children Who Have Previously Been Vaccinated With PandemrixTM

9. August 2018 aktualisiert von: GlaxoSmithKline

Immunogenicity and Safety Study of GSK Biologicals' Seasonal (2010-2011) Influenza Vaccine FluarixTM in Adolescents Previously Vaccinated With GSK Biologicals' H1N1 Vaccine PandemrixTM

This study is designed to assess the immunogenicity, reactogenicity and safety following vaccination with GSK Biologicals' FluarixTM vaccine in children who have previously been vaccinated with one dose of PandemrixTM at the age of 10-17 years.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Tatsächlich)

77

Phase

  • Phase 4

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

  • Finnland
      • Tampere, Finnland, 33100
        • GSK Investigational Site

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

10 Jahre bis 18 Jahre (Kind, Erwachsene)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Subjects having previously been immunized with only one single dose of Pandemrix at the age of 10-17 years inclusive.
  • Subjects having received Pandemrix at least six months prior to study enrolment.
  • Subjects who the investigator believes that subject and/or parent(s)/Legally Acceptable Representative(s) [LAR(s)] can and will comply with the requirements of the protocol
  • Written informed consent obtained from the subject/ the parent(s)/LAR(s) of the subject.
  • Healthy subjects as established by medical history and clinical examination before entering into the study.
  • Subjects or Parent(s)/LAR(s) with access to a consistent means of telephone contact, land line or mobile, but NOT a pay phone or other multiple-user device

Exclusion Criteria:

  • Active participation in other clinical trials.
  • 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.
  • Planned administration of any vaccine 30 days prior and 30 days after any study vaccine administration.
  • 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.
  • Acute disease and/or fever at the time of enrolment:
  • Acute or chronic, clinically-significant pulmonary, cardiovascular, hepatic or renal functional abnormality, as determined by medical history and physical examination.
  • Administration of immunoglobulins and/or any blood products within the three months prior to the enrolment in this study, or planned use during the study.
  • Any confirmed or suspected immunosuppressive or immunodeficient condition based on medical history and physical examination
  • Any known or suspected allergy to any constituent of influenza vaccines; a history of anaphylactic-type reaction to any constituent of influenza vaccines; or a history of severe adverse reaction to a previous influenza vaccine.
  • History of seizures or progressive neurological disease.
  • Subjects having received an H1N1v pandemic vaccine other than Pandemrix or having received the 2010/2011 seasonal influenza vaccine.
  • If the subject is female and if she is of childbearing potential, she must practice adequate contraception for 30 days prior to vaccination, have a negative pregnancy test and continue such precautions for two months after completion of the vaccination series.
  • Child in care.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Verhütung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Fluarix Group
Subjects previously vaccinated with Pandemrix vaccine received 1 dose of Fluarix vaccine. All vaccines were administered in the deltoid region of the non-dominant arm on Day 0.
Biologisch: FluarixTM
One Intramuscular injection
Aktiver Komparator: Havrix Group
Subjects previously vaccinated with Pandemrix vaccine received 1 first dose of Havrix vaccine (subjects aged above 15 years) or Havrix-Junior vaccine (subjects aged 15 years and below). A second dose was given outside the study setting, at Month 6. All vaccines were administered in the deltoid region of the non-dominant arm on Day 0.
Biologisch: HavrixTM Junior (in subjects of 15 years old or below) or HavrixTM (in subjects above 15 years old)
Two Intramuscular injections

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Geometric Mean Antibody Titres for Haemagglutination Inhibition (HI) Antibodies Against Fluarix Vaccine Containing H1N1 Strain.
Zeitfenster: At Day 0 and Day 28

Fluarix vaccine strain was Flu A/California/7/2009 (H1N1).

Day 28 data were presented only for the Fluarix Group.

Titres were expressed as geometric mean antibody titre.
At Day 0 and Day 28
Number of Seropositive Subjects for Haemagglutination Inhibition (HI) Antibodies Against Fluarix Vaccine Containing H1N1 Strain.
Zeitfenster: At Day 0 and Day 28

Fluarix vaccine strain was Flu A/California/7/2009 (H1N1).

Seropositivity was assessed for subjects with an antibody titre assay cut-off value equal to or above 1:10.

Day 28 data was presented only for the Fluarix Group.
At Day 0 and Day 28
Number of Seroconverted Subjects for Haemagglutination Inhibition (HI) Antibodies Against Fluarix Vaccine Containing H1N1 Strain.
Zeitfenster: At Day 28

Fluarix vaccine strain was Flu A/California/7/2009 (H1N1).

A seroconverted subject was a subject who had either a pre-vaccination (Day 0) titre less than (< ) 1:10 and a post-vaccination titre greater than or equal to ( ≥) 1:40 or a pre-vaccination titre ≥ 1:10 and at least a 4-fold increase in post-vaccination titre.

Day 28 data were presented for the Fluarix Group only.
At Day 28
Number of Seroprotected Subjects for Haemagglutination Inhibition (HI) Antibodies Against Fluarix Vaccine Containing H1N1 Strain.
Zeitfenster: At Day 0 and Day 28

Fluarix vaccine strain was Flu A/California/7/2009 (H1N1).

A seroprotected subject was a subject with a serum HI titre ≥ 1:40 that usually is accepted as indicating protection.

Day 28 data were presented for the Fluarix Group only.
At Day 0 and Day 28
Mean Geometric Increase (MGI) for Haemagglutination Inhibition (HI) Antibodies Against Fluarix Vaccine Containing H1N1 Strain.
Zeitfenster: At Day 28

Fluarix vaccine strain was Flu A/California/7/2009 (H1N1).

MGI is defined as the geometric mean of the within-subject ratios of the post-vaccination reciprocal HI titre to the pre-vaccination (Day 0) reciprocal HI titre.

Day 28 data were presented for the Fluarix Group only.
At Day 28

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Geometric Mean Antibody Titres for Haemagglutination Inhibition (HI) Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 0 and Day 28

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Victoria/210/2009 (H3N2) and B/Brisbane/60/2008.

Day 28 data were presented for the Fluarix Group only.

Titres were expressed as geometric mean antibody titres (GMTs).
At Day 0 and Day 28
Geometric Mean Antibody Titres for Haemagglutination Inhibition (HI) Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 0 and at Month 6

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Victoria/210/2009 (H3N2) and B/Brisbane/60/2008.

Only data for the Flu A/California/7/2009 (H1N1) strain were presented for the Havrix Group.

Titres were expressed as geometric mean antibody titres (GMTs).
At Day 0 and at Month 6
Number of Seropositive Subjects for Haemagglutination Inhibition (HI) Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 0 and Day 28

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Victoria/210/2009 (H3N2) and B/Brisbane/60/2008.

Seropositivity was assessed for subjects with an antibody titre assay cut-off value equal to or above 1:10.

Day 28 data were presented for the Fluarix Group only.
At Day 0 and Day 28
Number of Seropositive Subjects for Haemagglutination Inhibition (HI) Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 0 and at Month 6

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Victoria/210/2009 (H3N2) and B/Brisbane/60/2008.

Seropositivity was assessed for subjects with an antibody titre assay cut-off equal to or above 1:10.

Only data for the Flu A/California/7/2009 (H1N1) strain were presented for the Havrix Group.
At Day 0 and at Month 6
Number of Seroconverted Subjects for Haemagglutination Inhibition (HI) Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 28

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Victoria/210/2009 (H3N2) and B/Brisbane/60/2008.

A seroconverted subject was a subject who had either a pre-vaccination (Day 0) titre less than (< ) 1:10 and a post-vaccination titre greater than or equal to ( ≥) 1:40 or a pre-vaccination titre ≥ 1:10 and at least a 4-fold increase in post-vaccination titre.

Day 28 data were presented for the Fluarix Group only.
At Day 28
Number of Seroconverted Subjects for Haemagglutination Inhibition (HI) Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Month 6

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Victoria/210/2009 (H3N2) and B/Brisbane/60/2008.

A seroconverted subject was a subject who had either a pre-vaccination (Day 0) titre < 1:10 and a post-vaccination titre ≥ 1:40 or a pre-vaccination titre ≥ 1:10 and at least a 4-fold increase in post-vaccination titre.

Only data for the Flu A/California/7/2009 (H1N1) strain were presented for the Havrix Group.
At Month 6
Number of Seroprotected Subjects for Haemagglutination Inhibition (HI) Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 0 and Day 28

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Victoria/210/2009 (H3N2) and B/Brisbane/60/2008.

A seroprotected subject was a subject with a serum HI titre ≥ 1:40 that usually is accepted as indicating protection.

Day 28 data were presented for the Fluarix Group only.
At Day 0 and Day 28
Number of Seroprotected Subjects for Haemagglutination Inhibition (HI) Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 0 and Month 6

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Victoria/210/2009 (H3N2) and B/Brisbane/60/2008.

A seroprotected subject was a subject with a serum HI titre ≥ 1:40 that usually is accepted as indicating protection.

Only data for the Flu A/California/7/2009 (H1N1) strain were presented for the Havrix Group.
At Day 0 and Month 6
Mean Geometric Increase (MGI) for Haemagglutination Inhibition (HI) Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 28

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Victoria/210/2009 (H3N2) and B/Brisbane/60/2008.

MGI is defined as the geometric mean of the within-subject ratios of the post-vaccination reciprocal HI titre to the pre-vaccination (Day 0) reciprocal HI titre.

Day 28 data were presented for the Fluarix Group only.
At Day 28
Mean Geometric Increase (MGI) for Haemagglutination Inhibition (HI) Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Month 6

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Victoria/210/2009 (H3N2) and B/Brisbane/60/2008.

MGI is defined as the geometric mean of the within-subject ratios of the post-vaccination reciprocal HI titre to the pre-vaccination (Day 0) reciprocal HI titre.

Only data for the Flu A/California/7/2009 (H1N1) strain were presented for the Havrix Group.
At Month 6
Geometric Mean Antibody Titres for Neutralising Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 0 and at Day 28

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Perth/16/09(H3N2) and B/Brisbane/60/2008.

Day 28 data were presented for the Fluarix Group only.

Titres were expressed as geometric mean antibody titres (GMTs).
At Day 0 and at Day 28
Geometric Mean Antibody Titres for Neutralising Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 0 and at Month 6

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Perth/16/09 (H3N2) and B/Brisbane/60/2008.

Titres were expressed as geometric mean antibody titres (GMTs).
At Day 0 and at Month 6
Number of Seroconverted Subjects for Neutralising Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Day 28

A seroconverted subject for neutralising antibodies was a subject with a minimum 4-fold increase in titre at post-vaccination.

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Perth/16/09 (H3N2) and B/Brisbane/60/2008.

Day 28 data were presented for the Fluarix Group only.
At Day 28
Number of Seroconverted Subjects for Neutralising Antibodies Against All Fluarix Vaccine Strains.
Zeitfenster: At Month 6

A seroconverted subject for neutralising antibodies was a subject with a minimum 4-fold increase in titre at post-vaccination.

Fluarix vaccine strains were Flu A/California/7/2009 (H1N1), A/Perth/16/09 (H3N2) and B/Brisbane/60/2008.

At Month 6, only data for the Flu A/California/7/2009 (H1N1) strain were presented for the Havrix Group.
At Month 6
Number of Subjects Reporting Any and Grade 3 Solicited Local Symptoms.
Zeitfenster: Within 7 days (Day 0 - Day 6) after vaccination
Solicited local symptoms assessed were pain, redness and swelling. Any = occurrence of any solicited local symptom regardless of intensity grade. Grade 3 pain = pain that prevented normal activity. Grade 3 redness/swelling = redness/swelling above 50 millimetres.
Within 7 days (Day 0 - Day 6) after vaccination
Number of Subjects Reporting Any and Grade 3 Solicited General Symptoms.
Zeitfenster: Within 7 days (Day 0 - Day 6) after vaccination

Solicited general symptoms assessed were arthralgia, fatigue, gastrointestinal symptoms, headache, myalgia, shivering, sweating, temperature (temperature = axillary temperature equal to or above 37.5 degrees Celsius).

Any = occurrence of any solicited general symptom regardless of intensity grade or relation to vaccination. Grade 3 symptom = general symptom that prevented normal activity. Grade 3 temperature = axillary temperature above 39.0 degrees Celsius.
Within 7 days (Day 0 - Day 6) after vaccination
Number of Days With Any Solicited Local Symptoms.
Zeitfenster: Within 7 days (Day 0 - Day 6) after vaccination

Solicited local symptoms assessed were pain, redness and swelling.

Inter-quartile range assessed was the 25th percentile and the 75th percentile.
Within 7 days (Day 0 - Day 6) after vaccination
Number of Days With Grade 3 Solicited Local Symptoms.
Zeitfenster: Within 7 days (Day 0 - Day 6) after vaccination

Solicited local symptoms assessed were pain and swelling.

Grade 3 redness/swelling = redness/swelling above 50 millimetres.

Inter-quartile range assessed was the 25th percentile and the 75th percentile.
Within 7 days (Day 0 - Day 6) after vaccination
Number of Days With Any Solicited General Symptoms.
Zeitfenster: Within 7 days (Day 0 - Day 6) after vaccination

Solicited general symptoms assessed were arthralgia, fatigue, gastrointestinal symptoms, headache, myalgia, shivering, sweating, temperature (temperature = axillary temperature equal to or above 37.5 degrees Celsius).

Inter-quartile range assessed was the 25th percentile and the 75th percentile.
Within 7 days (Day 0 - Day 6) after vaccination
Number of Days With Grade 3 Solicited General Symptoms.
Zeitfenster: Within 7 days (Day 0 - Day 6) after vaccination

Solicited general symptoms assessed were fatigue, gastrointestinal symptoms, headache and myalgia.

Grade 3 symptom = general symptom that prevented normal activity.

Inter-quartile range assessed was the 25th percentile and the 75th percentile.
Within 7 days (Day 0 - Day 6) after vaccination
Number of Subjects Reporting Any, Grade 3 and Related Unsolicited Adverse Events (AEs).
Zeitfenster: Within 28 days (Day 0 - Day 27) after vaccination

An unsolicited adverse event is any adverse event (i.e. any untoward medical occurrence in a patient or clinical investigation subject, temporally associated with use of a medicinal product, whether or not considered related to the medicinal product) 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.

Grade 3 = event that prevented normal, everyday activities. Related = event assessed by the investigator as causally related to the study vaccination.
Within 28 days (Day 0 - Day 27) after vaccination
Number of Subjects Reporting Medically-attended Events (MAEs).
Zeitfenster: Within the 28-day (Days 0-27) post-vaccination period
For each solicited and unsolicited symptom the subject experienced, the subject was asked if they received medical attention defined as hospitalization, an emergency room visit or a visit to or from medical personnel for any reason.
Within the 28-day (Days 0-27) post-vaccination period
Number of Subjects Reporting Medically-attended Events (MAEs).
Zeitfenster: During the entire study period (Up to Month 6)
For each solicited and unsolicited symptom the subject experienced, the subject was asked if they received medical attention defined as hospitalization, an emergency room visit or a visit to or from medical personnel for any reason.
During the entire study period (Up to Month 6)
Number of Subjects Reporting Adverse Events of Specific Interest (AESIs)/Potential Immune Mediated Diseases (pIMDs).
Zeitfenster: During the entire study period (Up to Month 6)
Potential Immune-Mediated Diseases (pIMDs) or Adverse events of specific interest (AESI), are a subset of AEs that include both clearly autoimmune diseases and also other inflammatory and/or neurologic disorders which may or may not have an autoimmune etiology.
During the entire study period (Up to Month 6)
Number of Subjects Reporting Adverse Events of Special Interest.
Zeitfenster: During the entire study period (Up to Month 6)
Adverse events of special interest for safety monitoring includes both convulsion and anaphylaxis.
During the entire study period (Up to Month 6)
Number of Subjects Reporting Serious Adverse Events (SAEs).
Zeitfenster: Within the 28-day (Days 0-27) post-vaccination period
SAEs assessed include medical occurrences that results in death, are life threatening, require hospitalization or prolongation of hospitalization, results in disability/incapacity or are a congenital anomaly/birth defect in the offspring of a study subjects.
Within the 28-day (Days 0-27) post-vaccination period
Number of Subjects Reporting Serious Adverse Events (SAEs).
Zeitfenster: During the entire study period (Up to Month 6)
SAEs assessed include medical occurrences that results in death, are life threatening, require hospitalization or prolongation of hospitalization, results in disability/incapacity or are a congenital anomaly/birth defect in the offspring of a study subjects.
During the entire study period (Up to Month 6)

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

GlaxoSmithKline

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Nützliche Links

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

4. Oktober 2010

Primärer Abschluss (Tatsächlich)

7. Juli 2011

Studienabschluss (Tatsächlich)

7. Juli 2011

Studienanmeldedaten

Zuerst eingereicht

26. August 2010

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

26. August 2010

Zuerst gepostet (Schätzen)

27. August 2010

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

7. September 2018

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

9. August 2018

Zuletzt verifiziert

1. August 2017

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Zusätzliche relevante MeSH-Bedingungen

Andere Studien-ID-Nummern

  • 114452

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

JA

Beschreibung des IPD-Plans

Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.

Studiendaten/Dokumente

  1. Studienprotokoll
    Informationskennung: 114452
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  2. Klinischer Studienbericht
    Informationskennung: 114452
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  3. Statistischer Analyseplan
    Informationskennung: 114452
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  4. Einwilligungserklärung
    Informationskennung: 114452
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  5. Einzelner Teilnehmerdatensatz
    Informationskennung: 114452
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  6. Datensatzspezifikation
    Informationskennung: 114452
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

Klinische Studien zur FluarixTM

Suchen Sie nach ähnlichen Studien

Sponsoren und Mitarbeiter

Krankheiten

Drogeninterventionen

CROs by country

CROs in Bosnia & Herzegovina

Bedingungen

Seltene Krankheiten

Drogeninterventionen

Nahrungsergänzungsmittel

Sponsor / Mitarbeiter

Standorte

Abonnieren