Fasenra proven safe for Long-Term asthma control in Real-World study
NCT ID NCT03588546
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
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653 people
The number who actually took part.
- Started
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May 2018
- Finished
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Sep 2024
- Lead sponsor
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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
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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.
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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
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Research Site
Aichi, D3250C00057, Japan
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Research Site
Akita, D3250C00057, Japan
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Research Site
Aomori, D3250C00057, Japan
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Research Site
Chiba, D3250C00057, Japan
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Research Site
Ehime, D3250C00057, Japan
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Research Site
Fukuoka, D3250C00057, Japan
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Research Site
Gunma, D3250C00057, Japan
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Research Site
Hiroshima, D3250C00057, Japan
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Research Site
Hokkaido, D3250C00057, Japan
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Research Site
Hyōgo, D3250C00057, Japan
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Research Site
Ibaraki, D3250C00057, Japan
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Research Site
Kagawa, D3250C00057, Japan
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Research Site
Kagoshima, D3250C00057, Japan
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Research Site
Kanagawa, D3250C00057, Japan
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Research Site
Kumamoto, D3250C00057, Japan
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Research Site
Kyoto, D3250C00057, Japan
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Research Site
Mie, D3250C00057, Japan
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Research Site
Miyagi, D3250C00057, Japan
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Research Site
Numakunai, D3250C00057, Japan
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Research Site
Okayama, D3250C00057, Japan
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Research Site
Okinawa, D3250C00057, Japan
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Research Site
Osaka, D3250C00057, Japan
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Research Site
Ōita, D3250C00057, Japan
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Research Site
Saitama, D3250C00057, Japan
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Research Site
Shiga, D3250C00057, Japan
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Research Site
Tochigi, D3250C00057, Japan
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Research Site
Tokyo, D3250C00057, Japan
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Research Site
Yamagata, D3250C00057, Japan
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Research Site
Yamaguchi, D3250C00057, Japan
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