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NCT03283319 · ClinicalTrials.gov registry record · Phase 2

Panblok H7 Vaccine Adjuvanted With AS03 or MF59

A Phase 2 study, sponsored by Biomedical Advanced Research and Development Authority.

Completed
Registry status
Phase 2
Development phase
366
Enrollment target

NCT03283319: Completed Phase 2 study, sponsored by Biomedical Advanced Research and Development Authority.

NCT03283319 is a Phase 2 study that has completed, run by Biomedical Advanced Research and Development Authority. The registered enrollment target is 366 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (175% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03283319, a Phase 2 study, has completed, sponsored by Biomedical Advanced Research and Development Authority.

COMPLETED
Registry status
Phase 2
Development phase
366 participants
Enrollment target

Study Summary

The main purpose of this study is to assess the safety and ability of a Panblok H7 influenza vaccine adjuvanted with AS03 or MF59 to generate an immune response after 2 doses separated by 28 days. Three different antigen dose levels of Panblok H7 will be tested.

Primary Outcome

Count of participants who experienced at least one of the following during at least one of the time frames specified: Solicited local reactions at the injection site: erythema/redness, induration/swelling, and pain

Interventions

  • BIOLOGICAL MF59
  • BIOLOGICAL 3.75 ug Panblok H7
  • BIOLOGICAL 7.5 ug Panblok H7
  • BIOLOGICAL 15 ug Panblok H7
  • BIOLOGICAL AS03

Trial Details

FieldValue
Enrollment Target 366 participants
Start Date 2017-09-20
Est. Completion 2018-11-09
Phase Phase 2

What the finished NCT03283319 record still lists

NCT03283319 is an interventional study that assigns participants to a tested intervention. The registered 366 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (175% higher).

The record links to 0 conditions, and to 5 interventions - of which MF59 is the first listed.

NCT03283319 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03283319 about?

NCT03283319 is a clinical study titled "Panblok H7 Vaccine Adjuvanted With AS03 or MF59". The main purpose of this study is to assess the safety and ability of a Panblok H7 influenza vaccine adjuvanted with AS03 or MF59 to generate an immune response after 2 doses separated by 28 days. Three different antigen dose levels of Panblok H7 will be tested.

What is the current status of trial NCT03283319?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 366 participants. The study started on 2017-09-20. Estimated completion is 2018-11-09.

What interventions are being tested in trial NCT03283319?

The interventions under investigation include: MF59 (BIOLOGICAL), 3.75 ug Panblok H7 (BIOLOGICAL), 7.5 ug Panblok H7 (BIOLOGICAL), 15 ug Panblok H7 (BIOLOGICAL), AS03 (BIOLOGICAL).

Who is sponsoring clinical trial NCT03283319?

This trial is sponsored by Biomedical Advanced Research and Development Authority, which has 10 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03283319's enrollment target sits among peer trials

366 121st of 2000 higher than 1,880 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03283319, the US trial registry maintained by the National Library of Medicine. NCT03283319 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.