Perfluorohexyloctane

(Miebo®)

Perfluorohexyloctane

Drug updated on 7/25/2024

Dosage FormOphthalmic solution (topical; 100% perfluorohexyloctane)
Drug ClassSemifluorinated alkanes
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of the signs and symptoms of dry eye disease (DED).

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Summary
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  • Perfluorohexyloctane (Miebo) is indicated for the treatment of the signs and symptoms of dry eye disease (DED).
  • The information is derived from a systematic review and meta-analysis, which analyzed six randomized controlled trials (RCTs).
  • Compared to control interventions, perfluorohexyloctane showed significant improvements in eye dryness score, ocular surface disease index, lipid layer thickness, and total corneal fluorescein staining.
  • Fewer ocular treatment-emergent adverse events were reported with perfluorohexyloctane compared to controls; however, it was slightly less effective in improving tear film break-up time.
  • High patient satisfaction was noted with perfluorohexyloctane tear substitutes according to the systematic review.
  • No specific population types or subgroup considerations were provided; the study appears to have adopted a general population of DED patients.

Product Monograph / Prescribing Information

Document TitleYearSource
Miebo (perfluorohexyloctane) Prescribing Information. 2023Bausch & Lomb Americas Inc., Bridgewater, NJ

Systematic Reviews / Meta-Analyses