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Dornase alfa (Pulmozyme)

University of Jena · FDA-approved active Small molecule

Dornase alfa is a recombinant human deoxyribonuclease that cleaves extracellular DNA in airway secretions, reducing mucus viscosity and improving clearance in cystic fibrosis lungs.

Dornase alfa is a recombinant human deoxyribonuclease that cleaves extracellular DNA in airway secretions, reducing mucus viscosity and improving clearance in cystic fibrosis lungs. Used for Cystic fibrosis with FEV1 ≥40% predicted, Improvement of pulmonary function in cystic fibrosis patients.

At a glance

Generic nameDornase alfa (Pulmozyme)
SponsorUniversity of Jena
Drug classRecombinant enzyme
TargetExtracellular DNA (deoxyribonucleic acid)
ModalitySmall molecule
Therapeutic areaPulmonology / Respiratory
PhaseFDA-approved

Mechanism of action

In cystic fibrosis patients, neutrophil-derived DNA accumulates in thick airway secretions, contributing to airway obstruction and chronic infection. Dornase alfa enzymatically degrades this extracellular DNA, reducing sputum viscosity and improving mucociliary clearance. This allows better airflow and reduces bacterial colonization and inflammation in the lungs.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results