Denufosol
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| Systematic (IUPAC) name | |
|---|---|
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[[(3S,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl] hydrogen phosphate | |
| Clinical data | |
| Legal status |
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| Routes of administration | Inhalation |
| Identifiers | |
| CAS Number |
211448-85-0  |
| ATC code | None |
| PubChem | CID 9875516 |
| ChemSpider | 8051201 |
| UNII |
5PC250KSSH |
| ChEMBL | CHEMBL1767407 |
| Synonyms |
INS37217 2'-Desoxycytidine (5')tetraphospho(5')uridine |
| Chemical data | |
| Formula | C18H27N5O21P4 |
| Molar mass | 773.32 g/mol |
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Denufosol (INN) is an inhaled drug for the treatment of cystic fibrosis, being developed by Inspire Pharmaceuticals and sponsored by the Cystic Fibrosis Foundation. It was tested in two Phase III clinical trials, TIGER-1 and TIGER-2. Initially, in the first Phase III trial, TIGER-1, the compound showed significant results as compared with placebo.[1] In the second Phase III trial, TIGER-2, the compound did not meet the primary endpoint, a significant change in baseline FEV1 (forced expiratory volume in one second) at the week 48 endpoint as compared to placebo.[2] As of 2011, no additional clinical studies are being conducted with the compound.
The drug was also investigated for the treatment of retinal detachment and other retinal diseases, but trials were terminated in 2006.[3]
Application
In Phase III studies, denufosol was orally inhaled by patients with cystic fibrosis three times a day using a jet nebulizer. To be effective, it had to reach the deeper parts of the lung (bronchioles), making it unsuitable for children under five years of age.[4]
Mechanism of action
Cystic fibrosis is characterised by a defect of the chloride channel CFTR (cystic fibrosis transmembrane conductance regulator) on epithelial cells in the lungs. The CFTR regulates the components of sweat, digestive juices, and mucus. Defects lead to a viscous, dehydrated mucus, hindering mucociliary clearance. Denufosol is an agonist at the P2Y2 subtype of purinergic receptors, an alternative chloride channel. Activating this alternate chloride channel theoretically increases ion transport in cystic fibrosis patients which compensates the effects caused by the non-functioning CFTR.[5]
Chemistry
Denufosol consists of two nucleosides (composed of a nucleobase and a sugar each), 2'-desoxycytidine and uridine, linked by four units of phosphoric acid. It is used in form of its tetrasodium salt.
References
- ↑ Accurso, F. J.; Moss, R. B.; Wilmott, R. W.; Anbar, R. D.; Schaberg, A. E.; Durham, T. A.; Ramsey, B. W.; the TIGER-1 Investigator Study Group (2010). "Denufosol Tetrasodium in Patients with Cystic Fibrosis and Normal to Mildly Impaired Lung Function". American Journal of Respiratory and Critical Care Medicine 183 (5): 627–634. doi:10.1164/rccm.201008-1267OC. PMID 21169471.
- ↑ Inspire Announces Results of Second Phase 3 Trial with Denufosol for Cystic Fibrosis
- ↑ Clinical trial number NCT00083967 for "Study of Denufosol (INS37217) in Subjects With Rhegmatogenous Retinal Detachment" at ClinicalTrials.gov
- ↑ H. Spreitzer (14 March 2011). "Neue Wirkstoffe – Denufosol". Österreichische Apothekerzeitung (in German) (6/2011): 10.
- ↑ Kellerman, D.; Rossi Mospan, A.; Engels, J.; Schaberg, A.; Gorden, J.; Smiley, L. (2008). "Denufosol: A review of studies with inhaled P2Y2 agonists that led to Phase 3". Pulmonary Pharmacology & Therapeutics 21 (4): 600–607. doi:10.1016/j.pupt.2007.12.003. PMID 18276176.
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