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Trial · NCT05874713

Study to Evaluate Safety and Immunogenicity of Different Priming and Booster Regimens With Adjuvanted H5N8 and/or H5N6 Influenza Vaccine in Adults

NCT05874713, Phase 2, Completed, Seqirus

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Study to Evaluate Safety and Immunogenicity of Different Priming and Booster Regimens With Adjuvanted H5N8 and/or H5N6 Influenza Vaccine in Adults. Trials, record NCT05874713. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05874713

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Study to Evaluate Safety and Immunogenicity of Different Priming and Booster Regimens With Adjuvanted H5N8 and/or H5N6 Influenza Vaccine in Adults
NCT number
NCT05874713
Status
Completed
Phases
Phase 2
Enrollment
480 participants, actual
Lead sponsor
Seqirus
Conditions
Influenza, Human, Infections, Respiratory Tract Infections, Virus Diseases, Infection Viral
Interventions
aH5N8c on Day 1, aH5N6c on Day 1, aH5N8c on Day 22, aH5N6c on Day 22, aH5N8c on Day 202
First posted
2023-05-25
Last updated
2024-12-13

Source ClinicalTrials.gov

Registered outcomes53

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryGeometric mean titer (GMT) of hemagglutination inhibition (HI) antibodies against H5N8 strain - Day 1Day 1GMT (HI) prevaccination
PrimaryGMT of HI antibodies against H5N8 strain - Day 22Day 22GMT (HI) 3 weeks post first priming vaccination
PrimaryGMT of HI antibodies against H5N8 strain - Day 43Day 43GMT (HI) 3 weeks post second priming vaccination
PrimaryGMT of HI antibodies against H5N8 strain - Day 202Day 202GMT (HI) pre booster vaccination
PrimaryGMT of HI antibodies against H5N8 strain - Day 209Day 209GMT (HI) 1 week post booster vaccination
PrimaryGMT of HI antibodies against H5N8 strain - Day 223Day 223GMT (HI) 3 weeks post booster vaccination
PrimaryGMT of HI antibodies against H5N6 strain - Day 1Day 1GMT (HI) prevaccination
PrimaryGMT of HI antibodies against H5N6 strain - Day 22Day 22GMT (HI) 3 weeks post first priming vaccination
PrimaryGMT of HI antibodies against H5N6 strain - Day 43Day 43GMT (HI) 3 weeks post second priming vaccination
PrimaryGMT of HI antibodies against H5N6 strain - Day 202Day 202GMT (HI) pre booster vaccination

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT05874713

GET https://conductscience.org/api/trials/v1/NCT05874713/registered?page=2