Safety and Immunogenicity of Adjuvanted Versus High-Dose Inactivated Influenza Vaccines in Older Adults
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 757
- 试验地点
- 8
- 主要终点
- Number of Participants With Adverse Events of Clinical Interest, Population 2
研究概览
简要总结
The overall aim of the study is to compare safety and immunogenicity of inactivated influenza vaccine (IIV), adjuvanted (FLUAD®) versus High-Dose inactivated influenza (Fluzone® High-Dose) vaccine in persons ≥65 years (20% aged ≥80 years). A prospective, randomized, blinded clinical trial that will be conducted during the 2017/2018 and 2018/2019 influenza seasons. During each season, approximately 220 older adults will be enrolled at Duke University Medical Center and 140 older adults at Boston University Medical Center. Eligible subjects will be randomized to receive either adjuvanted influenza vaccine or High-Dose influenza vaccine. All subjects will receive vaccine and provide a blood draw at Visit 1, and then return for a second blood draw without vaccination about 4 weeks later to assess for influenza antibody titers. A subset of 100 subjects at Duke will provide a third blood draw 6 months post-vaccination to assess for waning of influenza antibody titers. Subjects will record the occurrence of local and systemic reactions (including fever, pain, tenderness, swelling, redness, general systemic systems), unsolicited adverse events, medical care utilization, and changes in medications over 8 days following vaccination. In addition, serious adverse events and events of clinical interest will be assessed through 42 days post-vaccination. Health-related quality of life will be assessed pre-vaccination (Day 1) and on Days 3 and 9 post-vaccination.
详细描述
Full Analysis Population 1: Defined as all subjects who are randomized, vaccinated, and provide at least one day of complete data on the symptom diary.
Full Analysis Population 2: Defined as all subjects who are randomized and vaccinated.
Immunogenicity Population: Defined as subjects who received vaccine, provided baseline and Visit 4 blood draws of acceptable volume and quality within the protocol-defined time frame with no protocol violations affecting immunogenicity.
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
- Triple (Participant, Investigator, Outcomes Assessor)
盲法说明
Subject, study coordinators, and investigators will be blinded to the type of flu vaccine administered. Only the vaccinator will be unblinded.
入排标准
- 年龄范围
- 65 Years 至 —（Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Persons aged ≥65 years, living in the community
- •Intention of receiving IIV vaccine based on ACIP-CDC guidelines
- •Willing to provide written informed consent prior to initiation of any study procedures
- •Able to speak English
- •Able and willing to complete baseline assessments and questionnaires, and to allow information to be collected from their electronic medical record
- •Able and willing to complete post-vaccine assessments and questionnaires independently or with assistance
- •Able and willing to have blood drawn for the study
- •Able and willing to return in about one month for a follow-up visit including completing questionnaires and having another blood test
- •Access to and ability to use a phone, independently or with assistance
- •Adequate vision and motor skills to complete the diary form independently or with assistance.
- •Not living in a skilled nursing facility/nursing home/long term acute care facility
排除标准
- •IIV receipt during the current influenza season prior to study enrollment
- •Enrolled in this study during the 2017-18 (Year 1) influenza season
- •Note: Year 1 study participants will only be enrolled in Year 2 if they are participating in the sub-study on repeat vaccination
- •Has immunosuppression as a result of an underlying illness or treatment, or use of anti-cancer chemotherapy or radiation therapy within the preceding 12 months.
- •Has an active neoplastic disease (excluding non-melanoma skin cancer or prostate cancer that is stable in the absence of therapy) or a history of any hematologic malignancy*
- •*Participants with a history of malignancy may be included if, after previous treatment by surgical excision, chemotherapy or radiation therapy, the participant has been observed for a period that in the investigator's estimation provides a reasonable assurance of sustained cure (not less than 12 months)
- •Thrombocytopenia, bleeding disorder, or anticoagulant use contraindicating intramuscular injection
- •History of febrile illness (> 100.0°F or 37.8°C) within the past 24 hours prior to IIV administration (temporary deferral)
- •Contraindication to IIV receipt including history of severe allergic reaction after a previous dose of any influenza vaccine; or to a vaccine component*, including egg protein; or a latex allergy
- •*Formaldehyde, Octylphenol ethoxylate, neomycin, kanamycin, barium, cetyltrimethlyammonium bromide (CTAB)
- •Any history of Guillain-Barré syndrome
- •Mild to severe dementia as determined by the Mini-Cog tool and the Rowland Universal Dementia Assessment Scale (RUDAS)
- •Substance use that could interfere with study compliance
- •Receipt of any inactivated licensed vaccine within 2 weeks, or live attenuated licensed vaccine within 4 weeks prior to enrollment in this study, or planning receipt of any vaccines during the 42-days post-vaccination period (including pneumococcal vaccines)
- •Anyone who is already enrolled or plans to enroll in another clinical trial with an investigational product within 28 days of vaccine receipt. Co-enrollment in observational or behavioral intervention studies are allowed at any time while enrollment in a clinical trial involving an investigational product (other than vaccine) may occur after 30 days following vaccine receipt.
- •Hearing loss determined by the investigators to prevent successful communication over the phone
- •Any condition which, in the opinion of the investigators, may pose a health risk to the subject or interfere with the evaluation of the study objectives.
- •Anyone who is a relative or subordinate of any research study personnel.
结局指标
主要结局
Number of Participants With Adverse Events of Clinical Interest, Population 2
时间窗: 42 days post-vaccination and compared between the two groups.
The frequency and descriptions of adverse events of clinical interest observed in the two treatment groups.
Number of Participants With Injection-Site Pain in Arm That Was Vaccinated, Population 1
时间窗: Days 1 through 8 post-vaccination
Comparison of the proportion of subjects reporting moderate/severe injection site pain within the first week post-vaccination in both treatment groups.
Observed Serious Adverse Events in Both Treatment Groups, Population 2
时间窗: 42 days post-vaccination and compared between the two groups.
The frequency and descriptions of serious adverse events observed in the two treatment groups. No analytical analysis was completed.
Number of Participants With H3N2 HAI Seroconversion
时间窗: 29 days post-vaccination
H3N2 hemagglutination inhibition assay (HAI) seroconversion: The proportion of subjects achieving H3N2 seroconversion at day 29 (an HAI titer \> 1:40 at day 29 if the baseline titer is \< 1:10 or a four-fold rise in HAI titer if the baseline titer is \> 1:10) in the respective season's vaccine
次要结局
- Seroprotection - 65 and Older(Day 29 (28 days post-vaccination))
- Number of Participants With Local Reactions in Arm That Was Vaccinated - Full Study, Population 1(Days 1 through 8 post-vaccination)
- Seroprotection - Ages 65-79(Day 29 (28 days post-vaccination))
- Number of Participants With Systemic Reactions - Full Study Population, Population 1(Days 1 through 8 post-vaccination)
- Quality of Life - EQ-5D-5L - Ages 65 - 79(Pre-vaccination (Day 1), 2 days post-vaccination (Day 3))
- Quality of Life - EQ VAS -Full Population(Pre-vaccination (Day 1), 2 days post-vaccination (Day 3))
- Number of Participants With Local Reactions in Arm That Was Vaccinated - Ages 65 - 79, Population 1(Days 1 through 8 post-vaccination)
- Number of Participants With System Reactions - Ages 65 - 79, Population 1(Days 1 through 8 post-vaccination)
- Quality of Life - EQ VAS - Ages 65 - 79(Pre-vaccination (Day 1), 2 days post-vaccination (Day 3))
- Seroconversion - 65 and Older(Day 29 (28 days post-vaccination))
- Number of Participants With Local Reactions in Arm That Was Vaccinated - Ages 80 +, Population 1(Days 1 through 8 post-vaccination)
- Number of Participants With System Reactions - Ages 80 +, Population 1(Days 1 through 8 post-vaccination)
- Quality of Life - Late Life Function & Disability Instrument - Full Population(Pre-vaccination (Day 1), 2 days post-vaccination (Day 3))
- Quality of Life - EQ-5D-5L - Ages 80 +(Pre-vaccination (Day 1), 2 days post-vaccination (Day 3))
- Geometric Mean HAI Titer - Ages 65-79(Day 29 (28 days post-vaccination))
- Quality of Life - Late Life Function & Disability Instrument - Ages 65 - 79(Pre-vaccination (Day 1), 2 days post-vaccination (Day 3))
- Quality of Life - Late Life Function & Disability Instrument - Ages 80 +(Pre-vaccination (Day 1), 2 days post-vaccination (Day 3))
- Quality of Life - EQ-5D-5L -Full Population(Pre-vaccination (Day 1), 2 days post-vaccination (Day 3))
- Quality of Life - EQ VAS - Ages 80 +(Pre-vaccination (Day 1), 2 days post-vaccination (Day 3))
- Geometric Mean HAI Titer - 65 and Older(Day 29 (28 days post-vaccination))
- Seroconversion - Ages 65-79(Day 29 (28 days post-vaccination))
- Seroconversion - Ages 80 and Older(Day 29 (28 days post-vaccination))
- Seroprotection - Ages 80 and Older(Day 29 (28 days post-vaccination))
- Geometric Mean HAI Titer - Ages 80 and Older(Day 29 (28 days post-vaccination))