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NCT02957656 · ClinicalTrials.gov registry record · Phase 1

Safety and Immunogenicity of Priming With Live Attenuated A/H7N9 Influenza Virus Vaccine Followed By Inactivated A/H7N9 Influenza Virus Vaccine With AS03 Adjuvant

A Phase 1 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
Phase 1
Development phase
53
Enrollment target

NCT02957656 is a Phase 1 study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 53 participants.

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The verdict

NCT02957656, a Phase 1 study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
Phase 1
Development phase
53 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety and immunogenicity of one dose of H7N9 pandemic live attenuated influenza vaccine (H7N9 pLAIV) followed by AS03-adjuvanted H7N9 pandemic inactivated influenza vaccine (H7N9 pIIV).

Interventions

  • BIOLOGICAL H7N9 pIIV
  • BIOLOGICAL H7N9 pLAIV
  • BIOLOGICAL AS03 adjuvant

Trial Details

FieldValue
Enrollment Target 53 participants
Start Date 2016-12
Phase Phase 1

What the Registry Record Tells You About NCT02957656

The ClinicalTrials.gov registry entry for NCT02957656 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 53 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which H7N9 pIIV is the first listed.

NCT02957656 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02957656 about?

NCT02957656 is a clinical study titled "Safety and Immunogenicity of Priming With Live Attenuated A/H7N9 Influenza Virus Vaccine Followed By Inactivated A/H7N9 Influenza Virus Vaccine With AS03 Adjuvant". The purpose of this study is to evaluate the safety and immunogenicity of one dose of H7N9 pandemic live attenuated influenza vaccine (H7N9 pLAIV) followed by AS03-adjuvanted H7N9 pandemic inactivated influenza vaccine (H7N9 pIIV).

What is the current status of trial NCT02957656?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 53 participants. The study started on 2016-12.

What interventions are being tested in trial NCT02957656?

The interventions under investigation include: H7N9 pIIV (BIOLOGICAL), H7N9 pLAIV (BIOLOGICAL), AS03 adjuvant (BIOLOGICAL).

Who is sponsoring clinical trial NCT02957656?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.