The goal of this study is to establish that Flublok Quadrivalent is non-inferior to fully licensed (traditional approval status) quadrivalent inactivated influenza vaccine (IIV4) in protecting against laboratory-confirmed clinical influenza disease in the ≥50 year age population.
The goal of this study is to establish that Flublok Quadrivalent is non-inferior to fully licensed (traditional approval status) quadrivalent inactivated influenza vaccine (IIV4) in protecting against laboratory-confirmed clinical influenza disease in the ≥50 year age population. Real-time Polymerase Chain Reaction (rtPCR) will be used to confirm influenza infection and to type the strains involved, as molecular methodologies have been demonstrated to be more sensitive than other more traditional methodologies, e.g. culture. For rtPCR-positive clinical samples, reserved aliquots will be processed for culture, so that antigenic similarity to the HA present in study vaccines can be tested. In various clinical studies the investigators demonstrated that the immune response against the influenza A viruses is improved as a result of the higher hemagglutinin content. Furthermore, influenza virus disease and hospitalization associated with influenza-related illness in older adults (\> 50 years) was considerably reduced (90%) following vaccination with TIV, even though the circulating influenza A strain was antigenically dissimilar to that in the vaccine. However, more recently Skowronski et al. reported that the low influenza vaccine effectiveness in 2012-2013 was not associated with antigenic drift but was instead related to mutations in the egg-adapted H3N2 vaccine strain. Flublok manufactured using recombinant technology does not contain the mutations responsible for the reported lower effectiveness and may thus offer improved protection when mutations such as those described are induced in the process of adapting the influenza virus to growth in eggs.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
9,003
Intramuscular injection of vaccine
Intramuscular injection of vaccine
Number of Participants With rtPCR-confirmed Influenza-Like Illness
rtPCR-confirmed, protocol-defined Influenza-Like Illness (ILI) caused by any influenza strain that begins at least 14 days post-vaccination
Time frame: 14 days post vaccination through and up to 32 weeks post vaccination
Number of Participants With Culture-confirmed Influenza-Like Illness
Culture-confirmed protocol-defined Influenza-Like Illness (ILI) that begins at least 14 days post-vaccination caused by an influenza strain (identified from the same clinical sample) antigenically matched to those strains represented in the study vaccines. Protocol-defined ILI is defined as at least one of the following respiratory symptoms accompanied by at least one of the following systemic symptoms: Respiratory symptoms: sore throat, cough, sputm production, wheezing, difficulty breathing Systemic symptoms: fever, chills (shivering), tiredness (fatigue), headache, myalgia (muscle ache)
Time frame: 14 days post vaccination through and up to 32 weeks post vaccination
Number of Participants With Culture-confirmed CDC-defined Influenza-Like Illness
Culture-confirmed CDC-defined Influenza-Like Illness (ILI) that begins at least 14 days post-vaccination caused by an influenza strain (identified from the same clinical sample) antigenically matched to those in the study vaccines. CDC-defined ILI is defined as body temperature ≥100°F accompanied by cough and/or sore throat.
Time frame: 14 days post vaccination through and up to 32 weeks post vaccination
Number of Participants With rtPCR-confirmed CDC-defined Influenza-Like Illness
rtPCR-confirmed CDC-defined ILI that begins at least 14 days post-vaccination caused by any influenza strain.
Time frame: 14 days post vaccination through and up to 32 weeks post vaccination
Percentage of Participants With Seroconversion
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Coastal Clinical Research
Mobile, Alabama, United States
Clinical Research Consortium Arizona
Tempe, Arizona, United States
Baptist Health Center for Clinical Research
Little Rock, Arkansas, United States
Northern California Clinical Research Center
Redding, California, United States
Benchmark Research - Sacramento
Sacramento, California, United States
Benchmark Research - San Francisco
San Francisco, California, United States
Lynn Institute of the Rockies
Colorado Springs, Colorado, United States
Clinical Research Consulting
Milford, Connecticut, United States
Clinical Research of South Florida
Coral Gables, Florida, United States
Avail Clinical Research
DeLand, Florida, United States
...and 28 more locations
Seroconversion rates (SCR) for all four antigens in a preselected subset of subjects.
Time frame: Days 0 through 28
Number of Participants With Local Injection Site Reactogenicity
Solicited events of injection site reactogenicity reported during Day 0-7.
Time frame: Days 0 through 7
Number of Participants With Unsolicited Adverse Events
Unsolicited adverse events reported in the 28 days following vaccine administration.
Time frame: Days 0 through 28
Number of Participants With Serious Adverse Events (SAEs) and Medically-attended Adverse Events (MAEs)
Serious adverse events (SAEs) and medically-attended adverse events (MAEs) occurring during the period of follow-up through the influenza season (at least 6 months post-vaccination). A MAE is an event that prompts an unplanned visit to a medical professional for diagnosis and/or treatment.
Time frame: Day 0 through and up to 32 weeks post vaccination
Measure of Post-vaccination HAI GMTs
GMT titers for all four antigens in a preselected subset of subjects.
Time frame: Days 0 through 28
Number of Participants With Systemic Reactogenicity
Solicited events of systemic reactogenicity reported during Day 0-7.
Time frame: Days 0 through 7