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Dornase alfa
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Dornase alfa
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Clinical data | |
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Trade names | Pulmozyme |
AHFS/Drugs.com | Monograph |
MedlinePlus | a694002 |
License data |
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Pregnancy category |
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Routes of administration |
Inhalation |
ATC code | |
Legal status | |
Legal status | |
Identifiers | |
CAS Number | |
DrugBank |
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ChemSpider |
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UNII | |
KEGG | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.029.685 |
Chemical and physical data | |
Formula | C1321H1999N339O396S9 |
Molar mass | 29254.04 g·mol−1 |
NY (what is this?) (verify) |
Dornase alfa, sold under the brand name Pulmozyme, is used for the treatment of cystic fibrosis. It is a recombinant human deoxyribonuclease I (rhDNase), an enzyme which selectively cleaves DNA. Dornase alfa hydrolyzes the DNA present in sputum/mucus and reduces viscosity in the lungs, promoting improved clearance of secretions. It is produced in Chinese hamster ovary cells.
Medical uses
Dornase alfa is indicated for the management of people with cystic fibrosis to improve pulmonary function.
Society and culture
Legal status
Dornase alfa is an orphan drug.
Research
Dornase alfa has been shown to improve lung function in non-cystic fibrosis pre-term infants atelectasis.