FLUAD® vs. Fluzone® High-Dose Study

Duke University

Status and phase

Completed

Phase 4

Conditions

Adverse Drug Event

Quality of Life

Injection Site Reaction

Side Effect of Drug

Pain

Treatments

Biological: Fluzone® High-Dose

Biological: FLUAD®

Study type

Interventional

Funder types

Other

Other U.S. Federal agency

Identifiers

NCT03183908

Pro00083845

Details and patient eligibility

About

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.

Full description

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.

Enrollment

757 patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

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.