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Seasonal Influenza

Part of Orthomyxoviridae Infections

5 published articles · Updated continuously

Clinical Trial Landscape

Clinical Trials for Seasonal Influenza

14 trials tracked for Seasonal Influenza: 6 in phase 3 or 4 and 1 with published results. The most-cited published study has 84 citations.

14Trials tracked
6Phase 3 & 4
0Recruiting
1With published results
Phase distribution
Phase 4 1 Phase 3 5 Phase 2 7 Phase 1 1
  1. Phase 3 Study of mRNA-1010 Seasonal Influenza Vaccine in Adults Completed · 84 cited
  2. Phase 4 Safety of a Influenza Vaccine Produced Either in Mammalian Cell Culture or in Embryonated Hen Eggs in Adults and Elderly With and Without Underlying Medical Conditions, and Immunogenicity in a Subset of Subjects With Underlying Medical Conditions Completed
  3. Phase 3 A Study of mRNA-1010 Seasonal Influenza Vaccine in Adults Completed
  4. Phase 3 A Study of mRNA-1010 Seasonal Influenza Vaccine in Adults 50 Years Old and Older Completed
  5. Phase 3 Safety and Immunogenicity of Trivalent Subunit Inactivated Flu Vaccine Administered to Healthy Children and Adolescents 3 to 17 Years of Age Completed
  6. Phase 3 Safety Study of IV Peramivir in Hospitalized Subjects With Confirmed or Suspected Influenza Completed
Show 8 more trials
  1. Phase 2 A Study of mRNA-1011.1, mRNA-1011.2, and mRNA-1012.1 Candidate Seasonal Influenza Vaccines in Healthy Adults Completed
  2. Phase 2 Humoral and Cell Mediated Immunity and Safety of MF59C.1-adjuvanted Subunit Influenza Vaccine or a Conventional Subunit Influenza Vaccine in Previously Unvaccinated Healthy Subjects Completed
  3. Phase 2 A Study of mRNA-1020 and mRNA-1030 Seasonal Influenza Vaccines in Healthy Adults Completed
  4. Phase 2 A Study of mRNA-1010 Seasonal Influenza Vaccine in Healthy Adults Completed
  5. Phase 2 Safety and Immunogenicity of a Surface Antigen, Inactivated, Adjuvanted With MF59C.1, Seasonal Influenza Vaccine, Formulation 2009-2010 Completed
  6. Phase 2 Study to Evaluate Safety and Immunogenicity of Sub-unit Adjuvanted Influenza Vaccine Administered to Elderly Subjects, Formulation 2010-2011 Completed
  7. Phase 2 Study to Evaluate Safety and Immunogenicity of Sub-unit Adjuvanted Influenza Vaccine Administered to Elderly Subjects, Formulation 2011-2012 Completed
  8. Phase 1 First-in-Human Clinical Trial of a Mosaic Quadrivalent Influenza Vaccine Compared With a Licensed Inactivated Seasonal QIV in Healthy Adults Completed

Showing the 14 most-cited and recently-updated of 14 trials. Browse the full registry →

Trial data sourced from ClinicalTrials.gov. Counts describe the research landscape and are not a treatment recommendation. Informational only — not medical advice.

What the trials found For clinicians

Seasonal Influenza: what the trials found

Several established trials evaluated the immunogenicity and efficacy of mRNA-1010, a seasonal influenza vaccine. In a phase 3 trial (N=8411), mRNA-1010 induced seroconversion rates ranging from 34.9% to 64.4% across strains, with 92.0% to 96.7% of participants achieving HAI titers ≥1:40 2. Another large phase 3 trial (N=22502) reported seroconversion rates of 29.4% to 52.0% and HAI titers ≥1:40 in 85.5% to 94.8% of participants 3. A third phase 3 trial (N=6102) showed seroconversion rates of 32.4% to 80.1% and HAI titers ≥1:40 in 80.7% to 97.6% 4. However, in the efficacy analysis, mRNA-1010 did not significantly reduce the first episode of RT-PCR-confirmed influenza-like illness (ILI) caused by any seasonal influenza strain (142 vs 140 events; p=0.1715) 3. In a phase 1/2 trial (N=885), seroconversion rates with mRNA-1010 ranged from 4.9% to 90.2% depending on dose and strain 9.

A cell-derived influenza vaccine (cTIV) was compared to traditional TIV in a phase 4 trial (N=1398). Among subjects with underlying medical conditions, the percentages achieving HAI titers ≥40 after one vaccination ranged from 40% to 98% for cTIV and TIV, with seroconversion rates of 56% to 72% 1. A phase 3 trial (N=3116) of TIV reported seroconversion rates of 78% to 95% and HAI titers ≥40 in 48% to 97% of subjects 6. For the antiviral peramivir, a phase 3 trial (N=234) showed a change from baseline in influenza virus titer at 48 hours of -1.66 vs -1.47 5.

Recent results — preliminary, needs further review

  • A phase 2 trial (N=698) of mRNA-1011.1 reported geometric mean fold rises (GMFR) of anti-HA antibodies at day 29 ranging from 2.7 to 3.7 across strains, with seroconversion rates of 35.9% to 49.4% 7.
  • Another phase 2 trial (N=572) of mRNA-1030 showed GMFRs of 5.29 to 9.93 and seroconversion rates of 56.7% to 75.4% 8.
  • Several small phase 2 trials (N=63-84) evaluated MF59-adjuvanted subunit influenza vaccines. One trial (N=84) reported seroconversion rates of 53% to 100% and HI titers >1:40 in 57% to 100% 10. Three other trials (N=63-64) using FLUAD showed seroconversion or significant increase in SRH area ranging from 26% to 69% 11, 43% to 46% 12, and 27% to 61% 13.
  • A phase 1 trial (N=63) of an Adjuplex-adjuvanted vaccine (VRC-GENADJ0110-AP-NV) reported local and systemic reactogenicity within 7 days, with 0-12 participants reporting local symptoms and 1-13 reporting systemic symptoms across dose groups 14.

For the clinician treating this condition

  • mRNA-1010 induces robust antibody responses (seroconversion and HAI titers ≥1:40) across multiple phase 3 trials, but did not demonstrate significant efficacy against RT-PCR-confirmed ILI in one large trial 234.
  • Cell-derived and traditional TIV vaccines show comparable immunogenicity in subjects with underlying medical conditions and in general populations 16.
  • Peramivir reduces influenza virus titers at 48 hours compared to baseline 5.

AI synthesis of 14 cited trials, updated Jun 29, 2026. Informational only — not medical advice; trial data sourced from ClinicalTrials.gov. How we use AI.

HCP Mode — summaries include clinical detail, trial data, and statistical outcomes.
Patient Mode — summaries use plain language, avoiding clinical jargon.

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Questions about Seasonal Influenza

Can I get the RSV and seasonal influenza vaccines at the same time?

Yes, you can get the RSV and seasonal influenza vaccines at the same time. Research shows this is safe and does not reduce the effectiveness of the flu shot.

Full answer →