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Immunogenicity & Safety Study of Fluviral® (2010 - 2011 Season) in Adults Aged 18 to 60 Years and Over 60 Years

2018年5月9日 更新者:GlaxoSmithKline

Immunogenicity and Safety Study of GSK Biologicals' (GSK1536489A) Trivalent Split Virion Influenza Vaccine Fluviral® (2010 - 2011 Season) in Adults Aged 18 to 60 Years and Over 60 Years.

This study is designed to test the safety and immunogenicity of Fluviral® (2010 - 2011 Season) in adults aged 18 to 60 years and over 60 years.

研究概览

地位

完全的

条件

干预/治疗

研究类型

介入性

注册 (实际的)

120

阶段

  • 第三阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Quebec
      • Sherbrooke、Quebec、加拿大、J1H 1Z1
        • GSK Investigational Site

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Subjects who the investigator believes that they can and will comply with the requirements of the protocol.
  • Written informed consent obtained from the subject
  • Male and female adults, 18 to 60 years of age and over 60 years of age.
  • Satisfactory baseline medical assessment by history and physical examination
  • Comprehension of the study requirements, ability to comprehend and comply with procedures for collection of safety data, expressed availability for the required study period, and ability and willingness to attend scheduled visits.
  • 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:

  • Participation in previous year's (2009) Fluviral registration study
  • Administration of any influenza vaccine within 6 months preceding the study start (35 or more subjects in the >60 year old age stratum will be recruited from among those who did NOT receive any inactivated influenza vaccine in 2009-2010 season, i.e. seasonal TIV or pandemic H1N1v).
  • Administration of any other vaccine(s) within 30 days prior to study enrollment or during the study period. Subjects who receive such treatment after enrollment will be followed per protocol and included in the safety analysis, but excluded from the according-to-protocol cohort.
  • Clinically or virologically confirmed influenza infection within 1 year preceding the study start.
  • Use of any investigational or non-registered product (drug or vaccine) other than the study vaccine within 30 days preceding the dose of study vaccine, or planned use during the study period.
  • Acute disease at the time of enrollment. (Acute disease is defined as the presence of a moderate or severe illness with or without fever). All vaccines can be administered to persons with a minor illness such as diarrhea, mild upper respiratory infection with or without low-grade febrile illness, i.e. oral temperature <38.0°C.
  • Significant acute or chronic, uncontrolled medical or psychiatric illness. "Uncontrolled" is defined as:

    • Requiring institution of new medical or surgical treatment within one (1) month prior to study enrollment, or
    • Requiring the re-institution of a previously discontinued medication or medical treatment within one month prior to study enrollment, or
    • Requiring a change in medication dosage in the one month prior to study enrollment due to uncontrolled symptoms or drug toxicity (elective dosage adjustments in stable subjects are acceptable), or
    • Hospitalization or an event fulfilling the definition of a SAE within one month prior to study enrollment.
  • Any confirmed or suspected immunosuppressive condition including:

    • History of human immunodeficiency virus (HIV) infection,
    • Cancer or treatment for cancer, within 3 years of study enrollment. Persons with a history of cancer who are disease-free without treatment for 3 years or more are eligible.
  • History of renal impairment.
  • History of hepatic dysfunction due to hepatitis B, C or toxins including alcohol.
  • Complicated insulin-dependent diabetes mellitus.
  • Unstable cardiopulmonary disease requiring chronic medical therapy or associated with functional impairment.
  • Presence of blood dyscrasias, including hemoglobinopathies and myelo- or lymphoproliferative disorder.
  • Receipt of systemic glucocorticoids (prednisone >= 20 mg/day for more than 14 consecutive days) within 1 month of study enrollment, or any cytotoxic or immunosuppressive drugs within six months of study enrollment. Inhaled and topical steroids are allowed.
  • A history of any demyelinating disease including Multiple Sclerosis and Guillain-Barré syndrome.
  • Presence of an active neurological disorder.
  • History of chronic alcohol consumption and/or drug abuse.
  • Any significant disorder of coagulation that increases the risk of intramuscular injections or treatment with coumadin derivatives or heparin. Persons receiving prophylactic antiplatelet medications, e.g. low-dose aspirin, and without a clinically-apparent bleeding tendency are eligible.
  • Administration of immunoglobulins and/or any blood products within the three months preceding the administration of the study vaccine or planned during the study.
  • Any known or suspected allergy to any constituent of Fluviral (egg protein, thimerosal) and/or a history of anaphylactic type reaction to consumption of eggs, and/or reactions to products containing mercury (such as thimerosal).
  • A history of severe adverse reaction to a previous influenza vaccination.
  • Pregnant and/or lactating/nursing female.
  • Any condition which, in the opinion of the investigator, prevents the subject from participation in the study.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Fluviral A Group
Subjects aged between 18 and 60 years who received one dose of Fluviral vaccine at Day 0, administered intramuscularly in the deltoid region of the non-dominant arm.
Intramuscular injection, one dose
实验性的:Fluviral B Group
Subjects over 60 years of age who received one dose of Fluviral vaccine at Day 0, administered intramuscularly in the deltoid region of the non-dominant arm.
Intramuscular injection, one dose

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Geometric Mean Titers (GMTs) of Haemagglutination Inhibition (HI) Antibodies Against Fluviral Vaccine Strains.
大体时间:At Day 0 before vaccination
The Fluviral vaccine strains were A/California (H1N1), A/Victoria (H3N2) and B/Brisbane
At Day 0 before vaccination
Geometric Mean Titers (GMTs) of Haemagglutination Inhibition (HI) Antibodies Against Fluviral Vaccine Strains.
大体时间:At Day 21 after vaccination
The Fluviral vaccine strains were A/California (H1N1), A/Victoria (H3N2) and B/Brisbane
At Day 21 after vaccination
Number of Seroprotected Subjects for Antibodies Against Fluviral Vaccine Strains.
大体时间:At Day 0 before vaccination
A Seroprotected subject was defined as a subject with a serum haemagglutination inhibition (HI) antibody titer greater than or equal to 1:40.
At Day 0 before vaccination
Number of Seroprotected Subjects for Antibodies Against Fluviral Vaccine Strains.
大体时间:At Day 21 after vaccination
A Seroprotected subject was defined as a subject with a serum haemagglutination inhibition (HI) antibody titer greater than or equal to 1:40.
At Day 21 after vaccination
Number of Seroconverted Subjects for Antibodies Against Fluviral Vaccine Strains.
大体时间:At Day 21 after vaccination
A subject seroconverted for haemagglutination inhibition (HI) antibodies was defined as a subject with either a prevaccination (Day 0) HI antibody titer below 1:10 and a post-vaccination titer greater than or equal to 1:40 or a prevaccination titer greater than or equal to 1:10 and at least a 4-fold increase in post-vaccination titer.
At Day 21 after vaccination
Seroconversion Factor for Antibodies Against Fluviral Vaccine Strains.
大体时间:At Day 21 after vaccination
Seroconversion Factor (SCF) is defined as the fold increase in serum HI antibody GMTs post-vaccination (Day 21) compared to prevaccination (Day 0).
At Day 21 after vaccination

次要结果测量

结果测量
措施说明
大体时间
Number of Subjects With Solicited Local and General Symptoms After Administration of Fluviral.
大体时间:During a 4-days (Day 0-3) follow-up period after vaccination.
Solicited local symptoms assessed were pain, redness and swelling at the injection site. Solicited general symptoms assessed were bronchospasm, chills, cough, fatigue, headache, joint pain at other location, muscle aches, red eyes, sore throat, swelling of the face and temperature (defined as orally temperature equal or above 38.0 degrees Celcius)
During a 4-days (Day 0-3) follow-up period after vaccination.
Number of Subjects With Any, Grade 3 and Related Unsolicited Adverse Events (AEs)
大体时间:Within the 21-day post-vaccination period

Unsolicited adverse events (AE) covers any AE reported in addition to those solicited during the clinical study and any solicited symptoms with onset outside the specified period of follow-up for solicited symptoms.

Any = occurrence of any adverse event regardless of intensity grade or relationship to vaccination.

Grade 3 = an unsolicited AE that prevented normal everyday activity. Related = event assessed by the investigator as causally related to the vaccination.

Within the 21-day post-vaccination period
Number of Subjects Reporting Unsolicited Adverse Events (AEs).
大体时间:Within the 21-day post-vaccination period
Unsolicited AE covers any AE 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.
Within the 21-day post-vaccination period
Number of Subjects With Serious Adverse Events (SAEs)
大体时间:During the entire study period
SAEs assessed include medical occurences that results in death, are life threatening, require hospitalization or prolongation of hospitalization, result in disability/incapacity or are a congenital anomaly/birth defect in the offspring of a study subject.
During the entire study period

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2010年7月9日

初级完成 (实际的)

2010年7月31日

研究完成 (实际的)

2010年7月31日

研究注册日期

首次提交

2010年6月29日

首先提交符合 QC 标准的

2010年6月29日

首次发布 (估计)

2010年6月30日

研究记录更新

最后更新发布 (实际的)

2018年6月8日

上次提交的符合 QC 标准的更新

2018年5月9日

最后验证

2016年9月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

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

研究数据/文件

  1. 研究协议
    信息标识符:110628
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  2. 个人参与者数据集
    信息标识符:110628
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  3. 统计分析计划
    信息标识符:110628
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  4. 知情同意书
    信息标识符:110628
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  5. 临床研究报告
    信息标识符:110628
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  6. 数据集规范
    信息标识符:110628
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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