Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Fasenra proven safe for Long-Term asthma control in Real-World study

NCT ID NCT03588546

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study looked at the long-term safety and effectiveness of Fasenra (benralizumab) in 653 people with severe asthma that wasn't controlled by other treatments. Researchers tracked side effects and asthma control over time. The goal was to confirm that Fasenra works well and is safe for long-term use in everyday medical practice.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Fasenra (benralizumab)
What this could lead to
If successful, this study confirms that Fasenra is safe and effective for long-term asthma control, helping patients manage their condition better.
What could go wrong
This is a post-marketing observational study, not a new treatment test. It may not show major new benefits, and individual results can vary.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

653 people

The number who actually took part.

Started

May 2018

Finished

Sep 2024

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The patients treated with Fasenra for the first time due to "Bronchial asthma (only the patients with intractable bronchial asthma which could not be controlled with the existing therapy).

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: -The evaluable patients treated with Fasenra for the first time due to "Bronchial asthma (only the patients with intractable bronchial asthma which could not be controlled with the existing therapy). Exclusion Criteria: -No past history of hypersensitivity to the components of Fasenra.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Asthma are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Research Site

    Aichi, D3250C00057, Japan

  • Research Site

    Akita, D3250C00057, Japan

  • Research Site

    Aomori, D3250C00057, Japan

  • Research Site

    Chiba, D3250C00057, Japan

  • Research Site

    Ehime, D3250C00057, Japan

  • Research Site

    Fukuoka, D3250C00057, Japan

  • Research Site

    Gunma, D3250C00057, Japan

  • Research Site

    Hiroshima, D3250C00057, Japan

  • Research Site

    Hokkaido, D3250C00057, Japan

  • Research Site

    Hyōgo, D3250C00057, Japan

  • Research Site

    Ibaraki, D3250C00057, Japan

  • Research Site

    Kagawa, D3250C00057, Japan

  • Research Site

    Kagoshima, D3250C00057, Japan

  • Research Site

    Kanagawa, D3250C00057, Japan

  • Research Site

    Kumamoto, D3250C00057, Japan

  • Research Site

    Kyoto, D3250C00057, Japan

  • Research Site

    Mie, D3250C00057, Japan

  • Research Site

    Miyagi, D3250C00057, Japan

  • Research Site

    Numakunai, D3250C00057, Japan

  • Research Site

    Okayama, D3250C00057, Japan

  • Research Site

    Okinawa, D3250C00057, Japan

  • Research Site

    Osaka, D3250C00057, Japan

  • Research Site

    Ōita, D3250C00057, Japan

  • Research Site

    Saitama, D3250C00057, Japan

  • Research Site

    Shiga, D3250C00057, Japan

  • Research Site

    Tochigi, D3250C00057, Japan

  • Research Site

    Tokyo, D3250C00057, Japan

  • Research Site

    Yamagata, D3250C00057, Japan

  • Research Site

    Yamaguchi, D3250C00057, Japan

More trials for these conditions

Other studies related to the condition(s) this trial covers.