跳至主要内容
临床试验/NCT04137887
NCT04137887终止3 期

Relative Effectiveness of a High-Dose Quadrivalent Influenza Vaccine Versus a Standard-Dose Quadrivalent Influenza Vaccine in Subjects 65 Years of Age and Older

Sanofi Pasteur, a Sanofi Company1 个研究点 分布在 1 个国家目标入组 33,096 人开始时间: 2019年11月4日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
终止
入组人数
33,096
试验地点
1
主要终点
Number of Participants With Hospitalizations Due to Cardiovascular or Respiratory Diseases

研究概览

简要总结

Primary Objective:

To demonstrate the superior relative effectiveness of QIV-HD as compared to QIV-SD among persons 65 years of age and older for the prevention of cardiovascular and/or respiratory hospitalizations.

Secondary Objective:

  • To assess the clinical relative effectiveness of QIV-HD as compared to QIV-SD in prevention of:
  • inpatient hospitalization for selected circulatory and respiratory causes
  • death, either all-cause or cardiovascular or respiratory causes
  • inpatient hospitalization (using primary and secondary discharge diagnoses)
  • inpatient hospitalization (using admission diagnoses)
  • hospital emergency room visits
  • primary care visits to physician or
  • major acute cardiovascular events (MACE)
  • To assess the characteristics of inpatient hospitalization or hospital emergency room visits or primary care visits to physician by QIV-HD and QIV-SD groups.
  • To describe the clinical relative effectiveness of QIV-HD as compared to QIV-SD:
  • by age group and by group with specific comorbidities
  • for different periods of observation
  • To describe all serious adverse events (SAEs) (including adverse event of special interest [AESIs]) for all subjects in both QIV-HD and QIV-SD groups.

详细描述

Study duration per participant was 1 day of screening and vaccination. The study was planned to be conducted over a period of 3 influenza seasons beginning in 2019-2020. The vaccination period was from October to December.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

Modified double-blind: the participants, the outcome assessors in the hospitals and outpatient care, the Investigators, and the Sponsor will remain blinded to the vaccine assignment in order to avoid any bias in reporting and evaluating illnesses or SAEs. An unblinded qualified trial staff member will administer the appropriate vaccine.

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Group 1: QIV-HD

Experimental

Participants received a single injection of 0.7 milliliters (mL) high dose quadrivalent influenza vaccine (QIV-HD), intramuscularly (IM) at Day 0.

干预措施: Quadrivalent Influenza Vaccine (split virion, inactivated) High-Dose (QIV-HD) (Biological)

Group 2: QIV-SD

Active Comparator

Participants received a single injection of 0.5 mL standard-dose quadrivalent influenza vaccine (QIV-SD), IM at Day 0.

干预措施: Standard-Dose Inactivated Influenza Vaccine Quadrivalent, Northern Hemisphere strains (QIV-SD) (Biological)

结局指标

主要结局

Number of Participants With Hospitalizations Due to Cardiovascular or Respiratory Diseases

时间窗: From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination)

Number of participants with hospitalizations due to any cardiovascular or respiratory diseases on the basis of International Classification of Diseases, Tenth Revision (ICD-10) codes as per health care professional (HCP) assessment were collected using Finnish health registers and reported in this outcome measure (OM). ICD-10 codes for respiratory system diseases: J00-J06 (acute upper respiratory infections), J09-J18 (influenza \& pneumonia), J20-J22 (other acute lower respiratory infections), J40-J47 (chronic lower respiratory diseases), J80-J81 (other respiratory diseases affecting interstitium), J85-J86 (suppurative \& necrotic conditions of lower respiratory tract); codes for circulatory diseases: I11 (hypertensive diseases), I20-I25 (ischemic heart diseases), I26-I27 (pulmonary heart disease \& diseases of pulmonary circulation), I30, I31, I33, I38-I42, I46-I50 (other forms of heart disease), I63-I67 (cerebrovascular diseases) \& I74 (diseases of arteries, arterioles \& capillaries).

Number of Participants With Primary Discharge Diagnoses For Any Respiratory and Circulatory Systems Diseases Hospitalizations

时间窗: From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination)

Number of participants with primary discharge diagnoses (final diagnosis given to participant before release from hospital) for any respiratory \& circulatory diseases hospitalizations on the basis of ICD-10 codes per HCP assessment were collected using Finnish health registers and reported in this OM. ICD-10 codes for respiratory system diseases were: J00-J06 (acute upper respiratory infections), J09-J18 (influenza \& pneumonia), J20-J22 (other acute lower respiratory infections), J40-J47 (chronic lower respiratory diseases), J80-J81 (respiratory diseases affecting interstitium), J85-J86 (suppurative \& necrotic conditions of the lower respiratory tract); and codes for circulatory system diseases were: I11 (hypertensive diseases), I20-I25 (ischemic heart diseases), I26-I27 (pulmonary heart disease \& diseases of pulmonary circulation), I30, I31, I33, I38-I42, I46-I50 (other heart disease), I63-I67 (cerebrovascular diseases) and I74 (diseases of arteries, arterioles and capillaries).

次要结局

  • Number of Participants With Primary Discharge Diagnoses for Various Respiratory and Circulatory Diseases(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Participants With Primary and Secondary Admission Diagnoses for Respiratory and Circulatory Diseases(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Participants With Primary and Secondary Discharge Diagnoses for Respiratory and Circulatory Diseases(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Participants With Hospitalizations Due to Cardiovascular or Respiratory Diseases: By Age Groups(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Participants With Hospitalizations Due to Cardiovascular or Respiratory Diseases: Groups With Specific Comorbidities(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Participants With Deaths(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Participants With Hospital Emergency Room Visits(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Participants With Acute Primary Care Visits to Physician(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Percentage of Observed Cardiorespiratory Events During the Assessment Period(14 to 30 days, 31 to 60 days, 61 to 90 days, 91 to 120 days and 121 days or above)
  • Duration of Cardiorespiratory Hospitalization(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Participants With Serious Adverse Events (SAEs), Serious Adverse Reactions (SARs), and Adverse Event of Special Interest (AESIs)(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Participants With Non-fatal SAEs(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Participants With Major Acute Cardiovascular Events (MACE)(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))
  • Number of Occurrences for Cardiorespiratory Diseases During Influenza Epidemic Period(From 14 days post-vaccination up to 31 May 2020 post-vaccination (i.e., up to a duration of 6 months post-vaccination))

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

终止
3 期
Study on a High-Dose Quadrivalent Influenza Vaccine Compared With Standard-Dose Quadrivalent Influenza Vaccine in Children 6 Months Through 35 Months of AgeInfluenza
NCT04544267Sanofi Pasteur, a Sanofi Company100
已完成
3 期
Study to Assess the Immune Response and the Safety Profile of a High-Dose Quadrivalent Influenza Vaccine (QIV-HD) Compared to a Standard-Dose Quadrivalent Influenza Vaccine (QIV-SD) in Japanese Adults 60 Years of Age and OlderInfluenza ImmunizationHealthy Volunteers
NCT04498832Sanofi Pasteur, a Sanofi Company2,100
进行中(未招募)
1 期
Study to Evaluate the Effectiveness of a High-Dose Quadrivalent Influenza Vaccine (QIV-HD) Compared to a Standard-Dose Quadrivalent Influenza Vaccine (QIV-SD) in Adults 65 Years of Age and OlderPrevention of influenza infection in adults from 65 years of age and olderMedDRA version: 20.0Level: PTClassification code 10022000Term: InfluenzaSystem Organ Class: 10021881 - Infections and infestations
EUCTR2019-001401-25-FISanofi Pasteur Inc.121,000
已完成
3 期
Study to Assess the Immune Response and the Safety Profile of a High-Dose Quadrivalent Influenza Vaccine (QIV-HD) Compared to a Standard-Dose Quadrivalent Influenza Vaccine (QIV-SD) in Taiwanese Adults 65 Years of Age and OlderInfluenza (Healthy Volunteers)
NCT04537234Sanofi Pasteur, a Sanofi Company165
已完成
3 期
Study to Assess the Immune Response and the Safety Profile of a High-Dose Quadrivalent Influenza Vaccine (QIV-HD) Compared to a Standard-Dose Quadrivalent Influenza Vaccine (QIV-SD) in Europeans Adults 60 Years of Age and OlderInfluenza ImmunizationHealthy Volunteers
NCT04024228Sanofi Pasteur, a Sanofi Company1,539