Allergic Bronchopulmonary Aspergillosis

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Review clinical trials related to Allergic Bronchopulmonary Aspergillosis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Real-World Effectiveness of Benralizumab in Allergic Bronchopulmonary Aspergillosis

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

Participants needed: 20
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Qianfoshan HospitalUpdated: Apr 21, 2026Locations: 2
Eligibility criteria

Clinical important pulmonary disease other than asthma with allergic bronchopulm...

Status: Recruiting

A Cohort Study of the Efficacy and Safety of Biologics in Patients With ABPA

To evaluate the efficacy and safety of biological agents in patients with allergic bronchopulmonary aspergillosis.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Qianfoshan HospitalUpdated: Apr 17, 2026Locations: 1Duration: 2 Years
Eligibility criteria

Meet the diagnostic criteria of allergic bronchopulmonary aspergillosis, accordi... [+4]

The underlying diseases were chronic obstructive pulmonary disease and bronchiec... [+6]

Status: Recruiting

Oral Itraconazole Versus Combination of Systemic Glucorticoids and Oral Itraconazole in CPA-ABPA Overlap Syndrome

While ABPA and CPA represent two distinct manifestations of Aspergillus-related lung disease, there is an overlap of investigations that are currently used for the diagnosis of these entities. In a previous study, the authors have demonstrated that 22% of subjects with CPA fulfilled the obligatory criteria for ABPA. While the preferable therapy in patients with ABPA is systemic glucocorticoids, the primary therapy in CPA is oral triazoles. However, a different management protocol in the "overlap group" with low doses of glucocorticoids and triazoles, needs to be systematically explored. In this study the investigators intend to compare the clinical outcomes in subjects with ABPA-CPA overlap treated either with oral azoles or a combination of systemic glucocorticoids and oral azoles.

Participants needed: 104
Trial details
Age: 15-90Biological sex: AllType: InterventionalSponsor: Post Graduate Institute of Medical Education and Research, ChandigarhUpdated: Apr 7, 2026Locations: 2
Eligibility criteria

Not listed

Status: Recruiting

A Study of the Efficacy and Safety of Bronchoscopic Airway Clearance and Amphotericin B Spraying in Patients With ABPA

To evaluate the efficacy and safety of bronchoscopic airway clearance and amphotericin B spraying in the treatment of allergic bronchopulmonary aspergillosis

Participants needed: 44
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Qianfoshan HospitalUpdated: Jan 23, 2026Locations: 1
Eligibility criteria

Meet the diagnostic criteria of allergic bronchopulmonary aspergillosis, accordi... [+2]

Allergic bronchopulmonary aspergillosis - serotype (i.e., meets the diagnostic c... [+8]

Status: Recruiting

iMagIng pulmonaRy Aspergillosis Using Gallium-68-dEferoxamine

This is a single center open-label feasibility trial involving a single study visit for participants. The purpose of the study is to demonstrate the feasibility of \[68Ga\]Ga-DFO-B PET/CT (gallium-68-deferoxamine) for the visualization of pulmonary Aspergillus infection. The incidence of fungal infections is on the rise and are associated with significant mortality. Diagnosis pulmonary aspergillosis can be can be challenging, often requiring invasive tests such as bronchoscopy and lung tissue biopsies. Molecular imaging, specifically using radiolabeled siderophores like \[68Ga\]Ga-DFO-B, offers a non-invasive and location-specific approach to visualize and evaluate infections. Siderophores, critical for pathogenic microbes like Aspergillus fumigatus, play a role in iron acquisition. Preclinical studies with radiolabeled deferoxamine (DFO-B) demonstrated distinct accumulation at infection sites. Additionally, \[68Ga\]Ga-DFO-B PET/CT may differentiate between Aspergillus infection and cancer, making it a promising non-invasive diagnostic tool for pulmonary aspergillosis.

Participants needed: 10
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Radboud University Medical CenterUpdated: May 22, 2025Locations: 1
Eligibility criteria

The patient is at least 18 years old on the day of inclusion. [+2]

The patient is pregnant or planning on becoming pregnant. [+4]

Status: Recruiting

A Randomized Trial of Prednisolone, Itraconazole, or Their Combination in Allergic Bronchopulmonary Aspergillosis

The investigators hypothesize that a combination of prednisolone and itraconazole would significantly reduce the exacerbation rate at one-year of patients with acute allergic bronchopulmonary aspergillosis (ABPA) compared to itraconazole or prednisolone monotherapy. In this study, 300 subjects aged ≥18 years with acute ABPA will be randomized to treatment with either prednisolone, itraconazole, or prednisolone plus itraconazole, all for four months each. After collecting baseline demographic, immunologic, and imaging data, the investigators will follow the patients every 2 months for the first two visits and then every four months for three visits. The primary outcome will be the proportion of subjects experiencing exacerbation (asthma or ABPA) 12 months after treatment completion.

Participants needed: 300
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Post Graduate Institute of Medical Education and Research, ChandigarhUpdated: Feb 28, 2025Locations: 1
Eligibility criteria

newly diagnosed subjects with uncontrolled asthma or symptoms or radiology sugge... [+1]

occurrence of ≥3 ABPA exacerbations in the last 18 months before enrollment [+10]

Status: Not yet recruiting

Multicenter Registration Study on Allergic Bronchopulmonary Aspergillosis

To understand the current diagnosis and treatment status of ABPA patients, observe their clinical characteristics, prognosis, and treatment outcomes, and identify the relevant factors for poor prognosis in patients.

Participants needed: 300
Trial details
Age: 18-85Biological sex: AllType: ObservationalSponsor: Peking University Third HospitalUpdated: Oct 16, 2024Locations: 1
Eligibility criteria

Not listed