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Phase 4 N=577 Randomized Single-blind Basic Science

Immunogenicity Trial of Recombinant Influenza Vaccine Among HCP in Israel

Influenza

Enrolled (actual)
577
Serious AEs
0.0%
Results posted
Nov 2023
Primary outcome: Primary: Post-vaccination Geometric Mean Titer Against Influenza Virus A/H1N1 — 173.1; 83.9 titers

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Flublok™ Quadrivalent by Sanofi, Inc. (Biological); VaxigripTetra™ by Sanofi, Inc. (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Centers for Disease Control and Prevention
Primary completion
Jan 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Post-vaccination Geometric Mean Titer Against Influenza Virus A/H1N1
173.1; 83.9
PRIMARY
Geometric Mean Titer Ratio (GMR) Against Influenza Virus A/H1N1
4.0; 1.9
PRIMARY
Post-vaccination Geometric Mean Titer Against Egg-grown Influenza Virus A/H3N2
241.9; 175.7
PRIMARY
Geometric Mean Titer Ratio (GMR) Against Egg-grown Influenza Virus A/H3N2
4.1; 2.4
PRIMARY
Post-vaccination GMT Against Cell-grown Influenza Virus A/H3N2
185.3; 86.7
PRIMARY
Geometric Mean Titer Ratio (GMR) Against Cell-grown Influenza Virus A/H3N2
6.1; 2.6
PRIMARY
Post-vaccination Geometric Mean Titer Against Influenza B(Victoria)
89.5; 76.0
PRIMARY
Geometric Mean Titer Ratio (GMR) Against Influenza B(Victoria)
1.9; 1.5
PRIMARY
Post-vaccination Geometric Mean Titer Against Influenza B(Yamagata)
191.1; 108.3
PRIMARY
Geometric Mean Titer Ratio (GMR) Against Influenza B(Yamagata)
2.7; 1.5

Summary

This randomized, open-label, active-controlled trial will assess humoral immune responses to a single dose of 2019-20 recombinant hemagglutinin quadrivalent influenza vaccines (RIV4) compared with standard egg-based unadjuvanted quadrivalent influenza vaccines (IIV4) among healthcare personnel (HCP) vaccinated during the previous 2018-19 season with IIV4. The trial will be conducted at two hospital sites in Israel during the 2019-20 influenza season among HCP who were enrolled in the Study of Healthcare Personnel with Influenza and other Respiratory Viruses in Israel (SHIRI).

Eligibility Criteria

Inclusion Criteria

  • Aged ≥18
  • Current member of Clalit Health Services
  • Consent to randomized receipt of influenza vaccination with either RIV4 or IIV4, or, if already vaccinated in the current year outside of the study, consent to receive a post-vaccination blood draw
  • Participated in the SHIRI study and received influenza vaccination during the 2018-19 influenza season (Group 1)
  • Participated in any year of the SHIRI study, not vaccinated in 2018-2019, but vaccinated in at least one study year (Group 1 supplemental)
  • Participated in the SHIRI study during all three years, regardless of vaccination status (Group 1 supplemental)
  • Participated in any year of the SHIRI study and had PCR-confirmed influenza virus infection during any of the three study years (Group 2)

Exclusion Criteria

  • Already received an influenza vaccine during the current influenza season
  • Not willing or able to get the flu vaccines being used in this study;
  • Previous hypersensitivity reaction to the study vaccines, or any vaccine, as reported by the subject
  • Received any non-influenza vaccine (e.g., Hepatitis B or other vaccine recommended for HCP) in the 4 weeks prior to the first study visit or plans to receive a vaccine in the 4 weeks following the first study visit
  • Currently participating in a study that involves an experimental agent (vaccine, drug, biologic, device, blood product, or medication), or has received an experimental agent within 1 month prior to enrollment in this study, or expects to receive an experimental agent during participation in this study.
  • Any condition or employment status that the potential participant or local study site principle investigator (PI) believes may interfere with successful completion of the study prior to December 2019, including being currently pregnant.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04523324). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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