Chemistry:Difluprednate

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Short description: Corticosteroid drug
Difluprednate
Difluprednate.svg
Difluprednate 3D.png
Clinical data
Trade namesDurezol
AHFS/Drugs.comMonograph
MedlinePlusa609025
License data
Routes of
administration
Eye drops
ATC code
Legal status
Legal status
Identifiers
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC27H34F2O7
Molar mass508.559 g·mol−1
3D model (JSmol)
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Difluprednate, sold under the brand name Durezol, is a corticosteroid used for the treatment of post-operative ocular inflammation and pain.[1]

It was approved for medical use in the United States in June 2008.[1][2][3] It is available as a generic medication.[4]

Medical uses

Difluprednate is indicated for the treatment of inflammation and pain associated with ocular surgery; and the treatment of endogenous anterior uveitis.[1]

Clinical trials

Difluprednate ophthalmic emulsion 0.05% is also being studied in other ocular inflammatory diseases, including a phase 3 study evaluating difluprednate for the treatment of anterior uveitis[5][6]

References

  1. 1.0 1.1 1.2 1.3 "Durezol emulsion". 11 July 2022. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d07b65d5-f8e3-4594-a7fb-108218746cec. 
  2. "Drug Approval Package: Durezol (Difluprednate) NDA #022212". 25 July 2008. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2008/022212s000TOC.cfm. 
  3. "Sirion Therapeutics Announces FDA Approval of Durezol for Treatment of Postoperative Ocular Inflammation and Pain" (Press release). Sirion Therapeutics, Inc. 2008-06-24. Retrieved 2008-06-30.
  4. "Competitive Generic Therapy Approvals". 29 June 2023. https://www.fda.gov/drugs/generic-drugs/competitive-generic-therapy-approvals. 
  5. Clinical trial number NCT00501579 for "Study of Difluprednate in the Treatment of Uveitis" at ClinicalTrials.gov
  6. "Difluprednate 0.05% versus prednisolone acetate 1% for endogenous anterior uveitis: a phase III, multicenter, randomized study". Investigative Ophthalmology & Visual Science 55 (5): 2993–3002. May 2014. doi:10.1167/iovs.13-12660. PMID 24677110.