Real-World asthma biologic use under the microscope in china
NCT ID NCT06605885
First seen Jun 27, 2026 · Last updated Aug 13, 2026 · Updated 2 times
Summary
This study follows 202 Chinese asthma patients who are already prescribed biologic medications. Researchers will track how consistently patients take their biologics over 52 weeks and describe treatment patterns. No new drug is being tested; the goal is to gather real-world data on biologic use and outcomes.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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202 people
The number who actually took part.
- Started
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Nov 2024
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- 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
Approximately 200 asthma patients will be enrolled in this study distributed among 50 sites in China.
- 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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Accepted
You do not need to have the condition being studied to take part.
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: 1. Chinese, Female or Male 2. Age: no limitation 3. Physician-confirmed asthma diagnosis with documented evidence of diagnosis or evidence of variable expiratory airflow limitation (e.g., from bronchodilator reversibility testing or other tests). 4. Participants or their legal guardians must be able to provide informed consent. 5. Prescription of asthma biologics at enrolment. Exclusion Criteria: 6. Participation in an interventional study within the last 3 months. 7. Any significant disease or disorder which, in the opinion of the investigator, may either put the patient at risk because of participation in the study with the usage of biologics, or may influence the results of the study, or the patient's ability to participate in the study
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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
Hohhot, China, China
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Research Site
Beijing, China
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Research Site
Changsha, China
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Research Site
Chengdu, China
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Research Site
Foshan, China
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Research Site
Fuzhou, China
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Research Site
Guangzhou, China
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Research Site
Hangzhou, China
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Research Site
Hefei, China
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Research Site
Jinan, China
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Research Site
Kunming, China
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Research Site
Nanchang, China
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Research Site
Nanjing, China
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Research Site
Ningbo, China
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Research Site
Qingdao, China
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Research Site
Quanzhou, China
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Research Site
Shanghai, China
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Research Site
Shenyang, China
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Research Site
Shenzhen, China
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Research Site
Shijiazhuang, China
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Research Site
Suining, China
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Research Site
Taiyuan, China
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Research Site
Tianjin, China
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Research Site
Ürümqi, China
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Research Site
Wenzhou, China
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Research Site
Wuhan, China
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Research Site
Wuxi, China
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Research Site
Xi'an, China
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Research Site
Zhengzhou, China
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Research Site
Zhuhai, China
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