What the trials found
Updated — new results
For clinicians
Influenza: what the trials found
Several influenza vaccine formulations have been evaluated for immunogenicity and safety. A live attenuated influenza vaccine (LAIV) demonstrated a geometric mean fold rise in HAI titers of 1.04, 1.49, and 1.09 1. A trivalent, Vero cell-derived vaccine showed seroconversion rates ranging from 36.8% to 68.3% and seroprotective antibody titers between 26.7% and 74.3% 2. Additionally, a live attenuated influenza vaccine was evaluated in a separate cohort 14, while other specific formulations including TIV [5, 9], Fluzone (various versions) [7, 10, 11, 12], FluBlok [13, 15], and Arepanrix 22 were established through various phases.
Specific clinical outcomes for influenza management include the use of Baloxavir Marboxil, which showed a reduction in participants requiring antibiotics for complications (1.6% vs 0%) and a significant decrease in positive influenza virus titers over time 3. Oseltamivir was evaluated and showed no statistically significant differences in clinical failure, ICU transfer within 24 hours, or re-hospitalization rates 17. High Dose Inactivated Influenza Vaccine (HDIV) demonstrated non-inferiority to Standard Dose Inactivated Influenza Vaccine (SDIV) regarding immunoprotection persistence at 6 months among residents of long-term care settings 16.
Vaccine safety and specific populations were also studied. The Fluzone Quadrivalent vaccine showed seroconversion rates between 78.9% and 88.6% with fever rates around 11-12% 18. FluMist demonstrated comparable Geometric Mean Titer (GMT) ratios between HCWA and SA subjects 19. In patients with asthma, the proportion of participants experiencing exacerbations or increased albuterol use was similar between LAIV4 and IIV4 21.
Arepanrix showed a geometric mean fold rise of 10.2 for HI antibodies against the A/California/7/2009 strain with minimal local symptoms 22.
Recent results — preliminary, needs further review
- Influenza Vaccine 1 demonstrated a Geometric Mean Fold-Rise (GMFR) of antibodies at Day 29 ranging from 1.8 to 3.7, with seroconversion rates between 22.2% and 50.0% 4.
For the clinician treating this condition
- Multiple vaccine platforms (LAIV, TIV, HDIV, FluBlok) are established for influenza prophylaxis, with varying levels of seroprotection and immunogenicity.
- Baloxavir Marboxil is associated with a reduction in the need for antibiotics due to influenza-related complications 3.
- Oseltamivir showed no significant difference in clinical failure or ICU transfer rates in the studied population 17.
- High Dose Inactivated Influenza Vaccine (HDIV) demonstrated non-inferiority to Standard Dose (SDIV) in long-term care settings 16.
AI synthesis of 11 cited trials,
updated Jun 21, 2026.
Informational only — not medical advice; trial data sourced from ClinicalTrials.gov.
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