ClinicalTrials.gg
Not yet recruitingNCT07828327Updated Sep 24, 2026

Real-World Effectiveness of Depemokimab in Allergic Bronchopulmonary Aspergillosis With Severe Eosinophilic Asthma

An interventional study of Depemokimab in Allergic Bronchopulmonary Aspergillosis, ABPA and Severe Eosinophilic Asthma, sponsored by Qianfoshan Hospital. Not yet recruiting at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-09-24.

Sponsored by Qianfoshan Hospital · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
01

Study summary

An open-label study will evaluate effects of Depemokimab in the treatment of severe eosinophilic asthma in patients with allergic bronchopulmonary aspergillosis

Read the detailed description

Subjects who have been identified to have severe eosinophilic asthma with ABPA will be consented and enrolled in the study to receive Depemokimab injections (100 mg subcutaneous) administered every 6 months.

02

Conditions studied

  • Allergic Bronchopulmonary Aspergillosis
  • ABPA
  • Severe Eosinophilic Asthma

Keywords

  • ABPA
  • Depemokimab
03

In context

Aspergillosis, Allergic Bronchopulmonary

42 studies on the registry are indexed under Aspergillosis, Allergic Bronchopulmonary; 13 are open to participants now.

This study's planned enrollment of 10 is below the median of 58 across 25 interventional studies indexed under Aspergillosis, Allergic Bronchopulmonary.

Browse Aspergillosis, Allergic Bronchopulmonary studies →

Lead sponsor

Qianfoshan Hospital is the lead sponsor of 144 studies on the registry; 75 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • History of allergy or 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.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Experimental
    Depemokimab treatment

    Depemokimab treatment will be given by injections administered every 6 months.

    Drug: Depemokimab

Interventions

06

What researchers measure

Primary outcomes

  1. Number of steroid requiring exacerbations

    Number of asthma exacerbations requiring the initiation of (or temporary increase in) systemic corticosteroids in severe eosinophilic asthma complicated by ABPA

    Time frame: 26 weeks

Secondary outcomes

  1. Patient-Reported Quality of Life as assessed by Saint George Respiratory Questionnaire

    The change from baseline score in Saint George Respiratory Questionnaire. The Saint George Respiratory Questionnaire (SGRQ) total score ranges from 0 to 100. Higher scores indicate a worse outcome (greater health impairment/poorer quality of life)

    Time frame: 26 weeks

  2. Asthma Control as assessed by Asthma Control Questionnaire 6

    The change from baseline score in Asthma Control Questionnaire 6. ACQ-6 scores range from 0 to 6, where higher scores represent poorer asthma control. A score ≤0.75 indicates well-controlled asthma, while a score ≥1.5 indicates uncontrolled asthma.

    Time frame: 26 weeks

  3. Lung Function (FEV1)

    The FEV1 change from baseline to End of Treatment

    Time frame: 26 weeks

07

Study locations

1 site
  • 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 250014, China
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07828327
Responsible party
Qian Qi (Prof., Qianfoshan Hospital) — Principal investigator
First posted
Sep 18, 2026
Start date
Nov 1, 2026 (estimated)
Primary completion
Feb 28, 2027 (estimated)
Completion
Aug 31, 2027 (estimated)
Last update
Sep 24, 2026

Study contacts

Qian Qi
Contact
qiqianqlh@163.com
+8613706380314

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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Studies of the drug tested here: Depemokimab

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