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A Study to Evaluate the Safety, Reactogenicity and Immunogenicity of GSK Biologicals' Non-typeable Haemophilus Influenzae (NTHi) Investigational Vaccine (GSK2838497A) in Current and Former Smokers

12 mai 2017 mis à jour par: GlaxoSmithKline

An Observer-blind Study to Evaluate the Safety, Reactogenicity and Immunogenicity of GSK Biologicals' Non-typeable Haemophilus Influenzae (NTHi) Investigational Vaccine (GSK2838497A) in Current and Former Smokers

The purpose of this study is to assess the safety, reactogenicity and immunogenicity of 8 different formulations of investigational NTHI vaccine in current and former smokers, 50-70 years of age.

Aperçu de l'étude

Description détaillée

This Protocol Posting has been updated following Protocol Amendment 1, dated 10 October 2012, leading to a change in an inclusion criterion.

Type d'étude

Interventionnel

Inscription (Réel)

272

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Antwerpen, Belgique, 2060
        • GSK Investigational Site
      • Gent, Belgique, 9000
        • GSK Investigational Site
      • Wilrijk, Belgique, 2610
        • GSK Investigational Site

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

50 ans à 70 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Subjects who, in the opinion of the investigator, can and will comply with the requirements of the protocol.
  • A male or female between, and including, 50 and 70 years of age at the time of the first vaccination.
  • Written informed consent obtained from the subject.
  • Subjects without medical history, clinical finding or laboratory finding which in the opinion of the investigator could pose a safety concern or interfere with the protocol.
  • Current or former smokers.
  • A smoking history of at least 10 pack-years.
  • 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 other than the study vaccines within 30 days preceding the first dose of study vaccine, or planned use during the study period.
  • 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 vaccine/product.
  • Planned administration/ administration of a vaccine not foreseen by the study protocol in the period starting 30 days before the first dose and ending 30 days after the last dose of vaccine, with the exception of any influenza vaccine which may be administered ≥ 15 days preceding or following any study vaccine dose.
  • Previous vaccination with any vaccine containing NTHi-antigens.
  • Chronic administration of immunosuppressants or other immune-modifying drugs within six months prior to the first vaccine dose. Topical steroids are allowed.
  • Administration of immunoglobulins and/or any blood products within the 3 months preceding the first dose of study vaccine or planned administration during the study period.
  • Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination.
  • History of or current autoimmune disease.
  • Post-bronchodilator Forced Expiratory Volume in 1 second (FEV1) < 80% of predicted normal value.
  • Diagnosed with a respiratory disorder. Please note that subjects with mild pulmonary obstruction can be enrolled.
  • Laboratory evidence of clinically significant haematological abnormalities at Screening.
  • Acute disease and/or fever at the time of enrolment.
  • Current alcoholism and/or drug abuse.
  • Has significant disease, in the opinion of the investigator, likely to interfere with the study and/or likely to cause death within the study duration.
  • History of or current condition preventing intramuscular injection as bleeding or coagulation disorder.
  • Has contraindication for spirometry testing.
  • Malignancies within previous 5 years and lymphoproliferative disorders.
  • Pregnant or lactating female.
  • Female planning to become pregnant or planning to discontinue contraceptive precautions.
  • Any other condition that the investigator judges may interfere with study findings.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Tripler

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Group A
Subjects in this group will receive formulation 1 of NTHi vaccine.
Intramuscular vaccination in the deltoid region of the non-dominant arm according to protocol schedule.
Expérimental: Group B
Subjects in this group will receive formulation 2 of NTHi vaccine.
Intramuscular vaccination in the deltoid region of the non-dominant arm according to protocol schedule.
Expérimental: Group C
Subjects in this group will receive formulation 3 of NTHi vaccine.
Intramuscular vaccination in the deltoid region of the non-dominant arm according to protocol schedule.
Expérimental: Group D
Subjects in this group will receive formulation 4 of NTHi vaccine.
Intramuscular vaccination in the deltoid region of the non-dominant arm according to protocol schedule.
Expérimental: Group E
Subjects in this group will receive formulation 5 of NTHi vaccine and a placebo.
Intramuscular vaccination in the deltoid region of the non-dominant arm according to protocol schedule.
Expérimental: Group F
Subjects in this group will receive formulation 6 of NTHi vaccine and a placebo.
Intramuscular vaccination in the deltoid region of the non-dominant arm according to protocol schedule.
Expérimental: Group G
Subjects in this group will receive formulation 7 of NTHi vaccine and a placebo.
Intramuscular vaccination in the deltoid region of the non-dominant arm according to protocol schedule.
Expérimental: Group H
Subjects in this group will receive formulation 8 of NTHi vaccine and a placebo.
Intramuscular vaccination in the deltoid region of the non-dominant arm according to protocol schedule.
Comparateur placebo: Group Placebo 1
Subjects in this group will receive placebo.
Intramuscular vaccination in the deltoid region of the non-dominant arm according to protocol schedule.
Comparateur placebo: Group Placebo 2
Subjects in this group will receive placebo.
Intramuscular vaccination in the deltoid region of the non-dominant arm according to protocol schedule.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Occurrence of each solicited local and general adverse event (AE), in all subjects, in all groups.
Délai: During a 7-day follow-up period (from day 0 to day 6) after each vaccination.
During a 7-day follow-up period (from day 0 to day 6) after each vaccination.
Occurrence of any unsolicited AE, in all subjects, in all groups.
Délai: During a 30-day follow-up period (from day 0 to day 29) after each vaccination.
During a 30-day follow-up period (from day 0 to day 29) after each vaccination.
Occurrence of haematological and biochemical laboratory abnormalities, in all subjects, in all groups.
Délai: Prior to each vaccination.
Prior to each vaccination.
Occurrence of haematological and biochemical laboratory abnormalities, in all subjects, in all groups.
Délai: 7 days after each vaccination.
7 days after each vaccination.
Occurrence of haematological and biochemical laboratory abnormalities, in all subjects, in all groups.
Délai: At study conclusion (Day 420).
At study conclusion (Day 420).
Occurrence of any serious adverse event (SAE), in all subjects, in all groups.
Délai: From first vaccination (Day 0) to study conclusion (Day 420).
From first vaccination (Day 0) to study conclusion (Day 420).
Occurrence of any potential immune-mediated disease (pIMD) in all subjects, in all groups.
Délai: From first vaccination (Day 0) to study conclusion (Day 420).
From first vaccination (Day 0) to study conclusion (Day 420).

Mesures de résultats secondaires

Mesure des résultats
Délai
Humoral immune response to the components of the NTHi vaccine formulations, in all subjects, in all groups, in terms of antibody concentrations.
Délai: Prior to each vaccination, 30 days after each vaccination, and at study conclusion (Day 420).
Prior to each vaccination, 30 days after each vaccination, and at study conclusion (Day 420).
Cell-mediated immune (CMI) responses to components of the NTHi vaccine formulations, in a sub-cohort of subjects, in all groups.
Délai: Prior to each vaccination, 30 days after each vaccination, and at study conclusion (Day 420).
Prior to each vaccination, 30 days after each vaccination, and at study conclusion (Day 420).

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

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Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

31 août 2012

Achèvement primaire (Réel)

30 janvier 2014

Achèvement de l'étude (Réel)

30 janvier 2014

Dates d'inscription aux études

Première soumission

23 août 2012

Première soumission répondant aux critères de contrôle qualité

30 août 2012

Première publication (Estimation)

5 septembre 2012

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

15 mai 2017

Dernière mise à jour soumise répondant aux critères de contrôle qualité

12 mai 2017

Dernière vérification

1 mai 2017

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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