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OpenTrials
Completed

NCT Number: NCT03994380

Use of DNAse in Neutrophilic Asthma

In this pilot protocol, the researchers look to determine benefits from use of nebulized rh-DNase for 4 weeks in patients with neutrophilic asthma.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

National Jewish Health

Denver, Colorado, 80206, United States

About this study

Patients with asthma of a non-Th2 phenotype have few advanced therapeutic options if their asthma remains poorly controlled despite adherence to guideline-based therapy. Currently, no targeted biologic therapies are available for neutrophilic asthma. The role of Recombinant human deoxyriboneuclease (rhDNase) has not been investigated in refractory asthma. rhDNase cleaves extracellular DNA released by neutrophils and other granulocytes, thereby reducing the viscosity of mucus. It is known that patients with asthma have higher levels of extracellular DNA than normals; however, these levels are lower than DNA levels found in the sputum of patients with cystic fibrosis. The benefits of rhDNase in cystic fibrosis have been well described. In these patients, use of daily nebulized rhDNase has shown improvement in lung function and reduction in exacerbations. Very little is known about DNAse use in asthmatics. Case reports have shown benefit when used in acute asthma exacerbations, but there are no data on its use as a therapy for neutrophilic asthma.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • i. Able to read and sign an Informed Consent Form (ICF)
  • ii. At least Age 18
  • iii. Diagnosis of Asthma with previous source documentation of PC 20 ≤ 16 mg/dl measured by FEV1 and/or reversibility with albuterol of ≥12% in FEV1
  • iv. pre-bronchodilator Forced Vital Capacity (FVC) less than 85% predicted AND Serum total MMP9 ≥ 1800 (cut off determined by previous clinical investigation- Medimmune) OR serum IL-8> 20 pg/ml OR Sputum extracellular DNA ≥ 3.8 µg/mL OR Sputum Neutrophils > 40%

Exclusion criteria

  • i. Pregnancy
  • ii. Current smoker, smoking within the past year or pack/year history ≥ 10
  • iii. Respiratory infection within past 6 weeks
  • iv. Antibiotics within the past 4 weeks
  • v. Active lung disease other than asthma
  • vi. Cancer within the past 5 years (excluding basal cell skin cancer)
  • vii. Chronic infection due to HIV, HBV, or HCV
  • viii. Hematologic or autoimmune disease
  • ix. Unable to safely undergo bronchoscopy as determined by primary or study doctor.

Treatment and study plan

RhDNAse Inhalation Solution

Drug

rhDNAse 2.5 mg nebulizer daily for 4 weeks

Primary outcomes

  1. Lung Function

    Time frame: 4 weeks

    FEV1

  2. Symptom Control

    Time frame: 4 weeks

    Asthma Control Test

Sponsors and collaborators

Lead sponsor

National Jewish Health

Other

Registry information

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Jun 21, 2019
Registry last updated
Apr 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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