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Pooled Analysis of Methodologically Harmonized Pragmatic Randomized Trials of High-Dose vs. Standard-Dose Influenza Vaccine Against Severe Clinical Outcomes

Pooled Analysis of Methodologically Harmonized Pragmatic Randomized Trials of High-Dose vs. Standard-Dose Influenza Vaccine Against Severe Clinical Outcomes

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06506812
Acronym
FLUNITY-HD
Enrollment
466320
Registered
2024-07-18
Start date
2025-05-31
Completion date
2025-08-31
Last updated
2025-09-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Influenza

Keywords

Influenza, Vaccination, Pragmatic, Registry, Pneumonia, Respiratory, Cardiovascular, Meta-analysis

Brief summary

This prespecified analysis will pool the datasets from two pragmatic randomized trials evaluating the relative vaccine effectiveness of high-dose vs. standard-dose influenza vaccine against severe clinical outcomes: the DANFLU-2 (A Pragmatic Randomized Trial to Evaluate the Effectiveness of High-Dose Quadrivalent Influenza Vaccine vs. Standard-Dose Quadrivalent Influenza Vaccine in Older Adults) trial and the GALFLU (Pragmatic Randomized Trial to Evaluate the Effectiveness of High-Dose Quadrivalent Influenza Vaccine vs. Standard-Dose Quadrivalent Influenza Vaccine in Adults Aged 65 to 79 Years in Galicia, Spain) trial. The purpose of the pooled analysis is to ensure adequate statistical power for evaluating relative vaccine effectiveness against severe clinical outcomes and to increase generalizability of the results by combining data from two countries.

Interventions

For this arm, the high-dose quadrivalent influenza vaccine Efluelda®/Fluzone® High-Dose Quadrivalent will be used.

Any standard-dose quadrivalent influenza vaccine administered in the governmental influenza vaccine programs may be used.

Sponsors

Sanofi
CollaboratorINDUSTRY
Hospital Clinico Universitario de Santiago
CollaboratorOTHER
Tor Biering-Sørensen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pragmatic trials conducted to estimate the relative vaccine effectiveness of high-dose influenza vaccine compared with standard-dose influenza vaccine using the DANFLU-2 protocol or a protocol developed based on the DANFLU-2 protocol

Exclusion criteria

* Low data quality * Influenza circulation threshold was not met in any of the study seasons * Severe under-enrollment in all seasons

Design outcomes

Primary

MeasureTime frame
Hospitalization for influenza or pneumonia≥14 days after vaccination up to 8 months

Secondary

MeasureTime frame
Laboratory-confirmed influenza hospitalization≥14 days after vaccination up to 8 months
All-cause hospitalization≥14 days after vaccination up to 8 months
Hospitalization for any cardio-respiratory disease≥14 days after vaccination up to 8 months
Hospitalization for influenza≥14 days after vaccination up to 8 months
Hospitalization for pneumonia≥14 days after vaccination up to 8 months
All-cause mortality≥14 days after vaccination up to 8 months

Other

MeasureTime frame
Hospitalization for myocardial infarction≥14 days after vaccination up to 8 months
Hospitalization for heart failure≥14 days after vaccination up to 8 months
Major adverse cardiovascular events (MACE) defined as a composite of hospitalization for acute myocardial infarction, hospitalization for stroke, and cardiovascular death≥14 days after vaccination up to 8 months
MACE defined as a composite of hospitalization for acute myocardial infarction, hospitalization for stroke, hospitalization for heart failure, and cardiovascular death (alternate definition #1)≥14 days after vaccination up to 8 months
MACE defined as a composite of hospitalization for acute myocardial infarction, hospitalization for stroke, and all-cause death (alternate definition #2)≥14 days after vaccination up to 8 months
Hospitalization requiring mechanical ventilation≥14 days after vaccination up to 8 months
Laboratory-confirmed influenza≥14 days after vaccination up to 8 months
Laboratory-confirmed pneumococcal pneumonia≥14 days after vaccination up to 8 months
Laboratory-confirmed COVID-19≥14 days after vaccination up to 8 months
Cardio-respiratory mortality≥14 days after vaccination up to 8 months
Respiratory mortality≥14 days after vaccination up to 8 months
Cardiovascular mortality≥14 days after vaccination up to 8 months
In-hospital mortality≥14 days after vaccination up to 8 months
Intensive care unit admission≥14 days after vaccination up to 8 months
Any hospital contact associated with laboratory-confirmed influenza≥14 days after vaccination up to 8 months
Any exacerbation of pre-existing chronic obstructive pulmonary disease≥14 days after vaccination up to 8 months
Any exacerbation of pre-existing chronic obstructive pulmonary disease (alternate definition)≥14 days after vaccination up to 8 months
Severe exacerbation of pre-existing chronic obstructive pulmonary disease≥14 days after vaccination up to 8 months
Severe exacerbation of pre-existing chronic obstructive pulmonary disease (alternate definition)≥14 days after vaccination up to 8 months
Hospitalization for atrial fibrillation≥14 days after vaccination up to 8 months
Any exacerbation of pre-existing asthma (alternate definition)≥14 days after vaccination up to 8 months
Severe exacerbation of pre-existing asthma≥14 days after vaccination up to 8 months
Severe exacerbation of pre-existing asthma (alternate definition)≥14 days after vaccination up to 8 months
Exacerbation of pre-existing heart failure≥14 days after vaccination up to 8 months
Exacerbation of pre-existing heart failure (alternate definition)≥14 days after vaccination up to 8 months
Hospitalization for pericarditis≥14 days after vaccination up to 8 months
Hospitalization for myocarditis≥14 days after vaccination up to 8 months
New-onset dementia≥14 days after vaccination up to 8 months
Any exacerbation of pre-existing asthma≥14 days after vaccination up to 8 months
Hospitalization for stroke≥14 days after vaccination up to 8 months
Hospitalization for influenza or pneumonia (alternate definition)≥14 days after vaccination up to 8 months
Hospitalization for pneumonia (alternate definition)≥14 days after vaccination up to 8 months
Hospitalization for influenza (alternate definition)≥14 days after vaccination up to 8 months
Hospitalization for any respiratory disease≥14 days after vaccination up to 8 months
Hospitalization for any cardiovascular disease≥14 days after vaccination up to 8 months

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026