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Study to Evaluate the Immunogenicity and Safety of an Investigational Influenza (H1N1 Influenza Virus) Vaccine in Adults, Using Two Different Manufacturing Processes

21. august 2018 opdateret af: GlaxoSmithKline

Immunological Non-inferiority Between Two Process-manufactured Influenza Vaccines in Adults Aged 18 to 60 Years

The objective of this study is to evaluate the immunogenicity and safety of one or two doses of GSK Biologicals' investigational influenza vaccine GSK2340272A, manufactured using two different processes, in adults aged 18 to 60 years.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

300

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Sachsen
      • Dresden, Sachsen, Tyskland, 01307
        • GSK Investigational Site
      • Dresden, Sachsen, Tyskland, 01067
        • GSK Investigational Site
      • Freiberg, Sachsen, Tyskland, 09599
        • GSK Investigational Site
      • Leipzig, Sachsen, Tyskland, 04103
        • GSK Investigational Site

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 60 år (Voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • All subjects must satisfy ALL the following criteria at study entry:
  • A male or female aged 18 to 60 years of age at the time of the first vaccination.
  • Subjects who the investigator believes that they can and will comply with the requirements of the protocol.
  • Written informed consent obtained from the subject.
  • Satisfactory baseline medical assessment by history and physical examination.
  • Access to a consistent means of telephone contact, which may be either in the home or at the workplace, land line or mobile, but NOT a pay phone or multiple-user device.
  • 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 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 (drug or vaccine) other than the study vaccine within 30 days preceding the first dose of the study vaccine or planned use during the study period.
  • Presence of evidence of substance abuse or of neurological or psychiatric diagnoses which, although stable, are deemed by the investigator to render the potential subject unable/unlikely to provide accurate safety reports.
  • Presence of an axillary temperature >= 37.5°C (99.5°F), or acute symptoms greater than "mild" severity on the scheduled date of first vaccination.
  • Clinically or virologically confirmed influenza infection within 6 months preceding the study start.
  • Diagnosed with cancer, or treatment for cancer, within 3 years.
  • Any confirmed or suspected immunosuppressive or immunodeficient condition including history of human immunodeficiency virus (HIV) infection.
  • Chronic administration of immunosuppressants or other immune modifying drugs within 6 months of study enrolment or planned administration during the study period.
  • Receipt of any immunoglobulins and/or any blood products within 3 months of study enrolment or planned administration of any of these products during the study period.
  • Any significant disorder of coagulation or treatment with coumarin derivatives, other vitamin K antagonists or heparin. Persons receiving individual doses of low molecular weight heparin outside of 24 hours prior to vaccination are eligible. Persons receiving prophylactic antiplatelet medications, e.g., low-dose acetylsalicylic acid, and without a clinically-apparent bleeding tendency, are eligible.
  • Any contraindication to intramuscular administration of the influenza vaccines.
  • An acute evolving neurological disorder or history of Guillain-Barré syndrome.
  • Administration of any vaccines within 30 days before vaccination.
  • 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.
  • Pregnant or lactating female
  • Female planning to become pregnant or planning to discontinue contraceptive precautions.
  • Any conditions which, in the opinion of the investigator, prevents the subjects from participating in the study.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Tredobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: GSK2340272A New 1D Group
Healthy male or female adults, between and including 18 to 60 years of age, who received one dose of the New process-manufactured (New 1D) GSK2340272A vaccine, administered intramuscularly in the deltoid region of the non-dominant arm at Day 0.
One intramuscular injection of initial process-manufactured GSK2340272A vaccine
Two intramuscular injections of initial process-manufactured GSK2340272A vaccine
One intramuscular injection of new process-manufactured GSK2340272A vaccine
Two intramuscular injections of new process-manufactured GSK2340272A vaccine
Eksperimentel: GSK2340272A New 2D Group
Healthy male or female adults, between and including 18 to 60 years of age, who received two doses of the New process-manufactured (New 2D) GSK2340272A vaccine, administered intramuscularly in the deltoid region of the non-dominant arm at Day 0 and of the dominant arm at Day 21.
One intramuscular injection of initial process-manufactured GSK2340272A vaccine
Two intramuscular injections of initial process-manufactured GSK2340272A vaccine
One intramuscular injection of new process-manufactured GSK2340272A vaccine
Two intramuscular injections of new process-manufactured GSK2340272A vaccine
Eksperimentel: GSK2340272A INI 1D Group
Healthy male or female adults, between and including 18 to 60 years of age, who received one dose of the Initial process-manufactured (INI 1D) GSK2340272A vaccine, administered intramuscularly in the deltoid region of the non-dominant arm at Day 0.
One intramuscular injection of initial process-manufactured GSK2340272A vaccine
Two intramuscular injections of initial process-manufactured GSK2340272A vaccine
One intramuscular injection of new process-manufactured GSK2340272A vaccine
Two intramuscular injections of new process-manufactured GSK2340272A vaccine
Eksperimentel: GSK2340272A INI 2D Group
Healthy male or female adults, between and including 18 to 60 years of age, who received two doses of the Initial process-manufactured (INI 2D) GSK2340272A vaccine, administered intramuscularly in the deltoid region of the non-dominant arm at Day 0 and of the dominant arm at Day 21.
One intramuscular injection of initial process-manufactured GSK2340272A vaccine
Two intramuscular injections of initial process-manufactured GSK2340272A vaccine
One intramuscular injection of new process-manufactured GSK2340272A vaccine
Two intramuscular injections of new process-manufactured GSK2340272A vaccine

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Number of Subjects Who Were Seroprotected for Haemagglutination Inhibition (HI) Antibodies Against the Flu A/California/7/2009 (H1N1) Virus Strain
Tidsramme: At Day 21
A seroprotected subject was defined as a vaccinated subject with a serum HI titer greater than or equal to (≥) 1:10, that usually is accepted as indicating protection.
At Day 21
Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against 2 Strains of Influenza Disease
Tidsramme: At Day 21
Titers are presented as geometric mean titers (GMTs). The flu strain assessed was Flu A/CAL/7/09. The reference seropositivity cut-off value was ≥ 1:10.
At Day 21

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Antal forsøgspersoner med alvorlige bivirkninger (SAE)
Tidsramme: I hele undersøgelsesperioden (fra dag 0 op til dag 364)
SAE'er, der vurderes, omfatter medicinske hændelser, der resulterer i dødsfald, er livstruende, kræver hospitalsindlæggelse eller forlængelse af hospitalsindlæggelse eller resulterer i invaliditet/invaliditet.
I hele undersøgelsesperioden (fra dag 0 op til dag 364)
Antal emner med alle, grad 3 og relaterede uopfordrede bivirkninger (AE'er)
Tidsramme: Inden for 21 dage efter den første vaccination og 63 dage efter den anden vaccination (dag 0 - dag 20 og dag 21 - dag 84)
En uopfordret bivirkning dækker enhver uønsket medicinsk hændelse i et klinisk forsøgsobjekt, der er midlertidigt forbundet med brugen af ​​et lægemiddel, uanset om det anses for at være relateret til lægemidlet og rapporteret ud over dem, der blev anmodet om under den kliniske undersøgelse, og ethvert anmodet symptom med indtræden udenfor den angivne periode for opfølgning for ønskede symptomer. Enhver blev defineret som forekomsten af ​​enhver uopfordret AE uanset intensitetsgrad eller relation til vaccination. Grad 3 AE = en AE, der forhindrede normale hverdagsaktiviteter. Relateret = AE vurderet af investigator som relateret til vaccinationen.
Inden for 21 dage efter den første vaccination og 63 dage efter den anden vaccination (dag 0 - dag 20 og dag 21 - dag 84)
Antal emner med alle og grad 3 anmodede lokale symptomer
Tidsramme: I løbet af den 7-dages (dage 0-6) post-vaccinationsperiode efter hver dosis og på tværs af doser
Vurderede opfordrede lokale symptomer var smerter, rødme og hævelse. Enhver = forekomst af symptom uanset intensitetsgrad. Grad 3 smerte = signifikant smerte i hvile; forhindret normale aktiviteter vurderet ved manglende evne til at deltage/gøre arbejde eller skole. Grad 3 rødme/hævelse = rødme/hævelse, der spreder sig ud over 100 millimeter (mm) af injektionsstedet.
I løbet af den 7-dages (dage 0-6) post-vaccinationsperiode efter hver dosis og på tværs af doser
Antal SCR-individer for HI-antistoffer
Tidsramme: På dag 182 og 364
Serokonversion blev defineret som: For initialt seronegative forsøgspersoner [antistoftiter under (<) 1:10 efter vaccination], antistoftiter større end eller lig med (≥) 1:40 efter vaccination; For initialt seropositive forsøgspersoner (antistoftiter ≥ 1:10 før vaccination), antistoftiter efter vaccination ≥ 4 gange antistoftiteren før vaccination. Den vurderede Flu-stamme var A/California/7/2009 (H1N1)v-lignende influenza (Flu A/CAL/7/09).
På dag 182 og 364
Antal forsøgspersoner, der blev serobeskyttet for HI-antistoffer mod influenza A/California/7/2009 (H1N1) virusstamme
Tidsramme: På dag 0, 21 og 42
Et serobeskyttet individ blev defineret som et vaccineret individ med en serum HI-titer større end eller lig med (≥) 1:40, hvilket sædvanligvis accepteres som indikerende beskyttelse.
På dag 0, 21 og 42
Antal forsøgspersoner, der blev serobeskyttet for HI-antistoffer mod influenza A/California/7/2009 (H1N1) virusstamme
Tidsramme: På dag 182 og 364
Et serobeskyttet individ blev defineret som et vaccineret individ med en serum HI-titer større end eller lig med (≥) 1:40, hvilket sædvanligvis accepteres som indikerende beskyttelse.
På dag 182 og 364
Geometrisk middelfoldningsstigning (GMFR) for HI-antistoffer mod influenza A/CAL/7/09-stamme af influenzasygdom
Tidsramme: På dag 21 og 42
GMFR blev defineret som foldstigningen i serum HI geometriske middeltitre (GMT'er) efter vaccination sammenlignet med prævaccination. Den vurderede influenzastamme var Flu A/CAL/7/09.
På dag 21 og 42
Geometrisk middelfoldningsstigning (GMFR) for HI-antistoffer mod influenza A/CAL/7/09-stamme af influenzasygdom
Tidsramme: På dag 182 og 364
GMFR blev defineret som foldstigningen i serum HI geometriske middeltitre (GMT'er) efter vaccination sammenlignet med prævaccination. Den vurderede influenzastamme var Flu A/CAL/7/09.
På dag 182 og 364
Antal fag med alle, grad 3 og relaterede anmodede generelle symptomer
Tidsramme: I løbet af den 7-dages (dage 0-6) post-vaccinationsperiode efter hver dosis og på tværs af doser
Vurderede anmodede generelle symptomer var træthed, hovedpine, ledsmerter andre steder, muskelsmerter, kulderystelser, svedtendens og feber [defineret som aksillær temperatur lig med eller over (≥) 37,5 grader Celsius (°C)]. Enhver = forekomst af symptom uanset intensitetsgrad eller forhold til vaccination. Grad 3 symptom = generelt symptom, der forhindrede normale hverdagsaktiviteter vurderet ved manglende evne til at deltage/gøre arbejde eller skole, eller krævet indgriben fra en læge/sundhedsplejerske. Grad 3 feber = temperatur > 39,0 °C og ≤ 40 °C. Relateret = symptom vurderet af investigator som relateret til vaccinationen.
I løbet af den 7-dages (dage 0-6) post-vaccinationsperiode efter hver dosis og på tværs af doser
Number of Subjects Who Were Seroprotected for HI Antibodies Against the Flu A/California/7/2009 (H1N1) Virus Strain
Tidsramme: At Days 0 and 42
A seroprotected subject was defined as a vaccinated subject with a serum HI titer greater than or equal to (≥) 1:40, that usually is accepted as indicating protection.
At Days 0 and 42
Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 Strain of Influenza Disease
Tidsramme: At Days 0 and 42
Titers are presented as geometric mean titers (GMTs). The flu strain assessed was Flu A/CAL/7/09. The reference seropositivity cut-off value was ≥ 1:10.
At Days 0 and 42
Number of Subjects Who Were Seroprotected for Haemagglutination Inhibition (HI) Antibodies Against the Flu A/California/7/2009 (H1N1) Virus Strain
Tidsramme: At Days 182 and 364
A seroprotected subject was defined as a vaccinated subject with a serum HI titer greater than or equal to (≥) 1:10, that usually is accepted as indicating protection.
At Days 182 and 364
Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against Flu A/California/7/2009 Strain of Influenza Disease
Tidsramme: At Days 182 and 364
Titers are presented as geometric mean titers (GMTs). The flu strain assessed was Flu A/CAL/7/09. The reference seropositivity cut-off value was ≥ 1:10.
At Days 182 and 364
Number of Seroconverted (SCR) Subjects for HI Antibodies
Tidsramme: At Days 21 and 42
Seroconversion was defined as: For initially seronegative subjects [antibody titer below (<) 1:10 post vaccination], antibody titer greater than or equal to (≥) 1:40 after vaccination; For initially seropositive subjects (antibody titer ≥ 1:10 prior to vaccination), antibody titer after vaccination ≥ 4 fold the pre-vaccination antibody titer. The Flu strain assessed was A/California/7/2009 (H1N1)v-like influenza (Flu A/CAL/7/09).
At Days 21 and 42
Number of Days With Solicited Local Symptoms
Tidsramme: During the 7-day (Days 0-6) post-vaccination period following each dose and overall
The number of days with any solicited local symptoms reported during the solicited post-vaccination period.
During the 7-day (Days 0-6) post-vaccination period following each dose and overall
Number of Days With Solicited General Symptoms
Tidsramme: During the 7-day (Days 0-6) post-vaccination period following each dose and overall
The number of days with any solicited general symptoms reported during the solicited post-vaccination period.
During the 7-day (Days 0-6) post-vaccination period following each dose and overall
Number of Subjects With Potential Immune-mediated Diseases (pIMDs)
Tidsramme: During the entire study period (from Day 0 up to Day 364)
Any pIMD was defined as an AE including autoimmune diseases and other mediated inflammatory disorders and assessed by the investigator as specific to the treatment administration. Related pIMD was defined as an event assessed by the investigator as possibly related to the study vaccination.
During the entire study period (from Day 0 up to Day 364)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

14. oktober 2009

Primær færdiggørelse (Faktiske)

9. november 2010

Studieafslutning (Faktiske)

9. november 2010

Datoer for studieregistrering

Først indsendt

8. oktober 2009

Først indsendt, der opfyldte QC-kriterier

8. oktober 2009

Først opslået (Skøn)

9. oktober 2009

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

31. januar 2019

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

21. august 2018

Sidst verificeret

1. maj 2018

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

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

Studiedata/dokumenter

  1. Klinisk undersøgelsesrapport
    Informations-id: 113809
    Oplysningskommentarer: For additional information about this study please refer to the GSK Clinical Study Register
  2. Formular til informeret samtykke
    Informations-id: 113809
    Oplysningskommentarer: For additional information about this study please refer to the GSK Clinical Study Register
  3. Datasætspecifikation
    Informations-id: 113809
    Oplysningskommentarer: For additional information about this study please refer to the GSK Clinical Study Register
  4. Statistisk analyseplan
    Informations-id: 113809
    Oplysningskommentarer: For additional information about this study please refer to the GSK Clinical Study Register
  5. Individuelt deltagerdatasæt
    Informations-id: 113809
    Oplysningskommentarer: For additional information about this study please refer to the GSK Clinical Study Register
  6. Studieprotokol
    Informations-id: 113809
    Oplysningskommentarer: For additional information about this study please refer to the GSK Clinical Study Register
  7. Annoteret sagsbetænkningsformular
    Informations-id: 113809
    Oplysningskommentarer: For additional information about this study please refer to the GSK Clinical Study Register

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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