Clinical Trials in China / NCT07828327
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Real-World Effectiveness of Depemokimab in Allergic Bronchopulmonary Aspergillosis With Severe Eosinophilic Asthma
NCT07828327 · tracked via the Priya Life Science China tracker
Condition(s) studied
Allergic Bronchopulmonary AspergillosisABPASevere Eosinophilic Asthma
Investigational drug(s) / intervention(s)
Depemokimab: 100 mg (1mL) Subcutaneous Solution
Study summary
An open-label study will evaluate effects of Depemokimab in the treatment of severe eosinophilic asthma in patients with allergic bronchopulmonary aspergillosis
Eligibility
Inclusion Criteria:
* Female and Male patients aged 18-75 years
* Diagnosis of Allergic Bronchopulmonary Aspergillosis (according to the ISHAM Working Group Diagnostic Criteria)
* Severe asthma requiring treatment with high dose ICS plus a long acting beta-agonist (LABA) or long-acting muscarinic antagonists (LAMA)), or maintenance OCS (daily or every other day OCS requirement in order to maintain asthma control)
Exclusion Criteria:
* History of allergy or hypersensitivity reaction to Depemokimab or any of its components.
* Currently pregnant, breastfeeding, or lactating women.
* Concurrent enrollment in another interventional or post-authorization safety study, unless it is observational.
Primary outcome measure(s)
- Number of steroid requiring exacerbations — 26 weeks
Number of asthma exacerbations requiring the initiation of (or temporary increase in) systemic corticosteroids in severe eosinophilic asthma complicated by ABPA
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Department of Respiratory, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, #16766, Jingshi Road, Jinan City, Shandong Province, China | Jinan | Shandong |
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Recruiting
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07828327 on ClinicalTrials.gov ↗ ← All trials in China