MedPath

Perfluorohexyloctane

Generic Name
Perfluorohexyloctane
Brand Names
Miebo
Drug Type
Small Molecule
Chemical Formula
C14H17F13
CAS Number
133331-77-8
Unique Ingredient Identifier
7VYX4ELWQM
Background

Perfluorohexyloctane is a semifluorinated alkane that contains six perfluorinated carbon atoms and eight hydrogenated carbon atoms. It is an inert, slightly amphiphilic compound. Because it is a completely non-aqueous liquid, microbial growth is not possible; therefore, its drug products do not need to be combined with any preservative.

Perfluorohexyloctane has been used in the field of ophthalmology as a vitreous substitute. It was approved by the FDA on May 18, 2023 for the treatment of dry eye disease.

Indication

Perfluorohexyloctane ophthalmic formulation is indicated for the treatment of the signs and symptoms of dry eye disease.

Associated Conditions
Dry Eye Syndrome (DES)
Associated Therapies
-
pharmaphorum.com
·

Aldeyra spies FDA filing ahead for dry eye drug reproxalap

Aldeyra Therapeutics is advancing with reproxalap for dry eye disease, despite mixed phase 3 trial results. After FDA discussions, it plans a US approval filing. Reproxalap showed rapid symptom improvement but faces competition from existing and emerging treatments like NOV03.
healio.com
·

The kids are alright: Miebo and Xdemvy at year 1

Miebo and Xdemvy, FDA-approved dry eye disease treatments, have significantly impacted DED care, outperforming phase 3 trials with positive patient results and minimal side effects. Miebo, addressing evaporation, sold $162.6M in its first year, while Xdemvy, targeting Demodex blepharitis, achieved $126M in sales, both showing rapid symptom relief and improved patient outcomes.
investing.com
·

Bausch + Lomb acquires glaucoma surgery innovator

Bausch + Lomb acquires Elios Vision, Inc., enhancing its glaucoma treatment portfolio with the ELIOS™ MIGS procedure, a clinically validated, implant-free surgery. The acquisition aims to address the rising glaucoma prevalence, leveraging Bausch + Lomb's global reach for widespread adoption. Despite strong financial performance, analysts express caution over stock valuation.
einpresswire.com
·

Drug Trials Snapshot: MIEBO

MIEBO is an ophthalmic solution for dry eye disease, administered 4 times daily. It was approved based on two clinical trials involving 1,217 patients. The trials showed MIEBO improved corneal surface and dryness symptom scores. Efficacy and side effects were consistent across sex, race, and age groups. Common side effects included blurred vision and headache.
frontiersin.org
·

Perfluorohexyloctane ophthalmic solution for dry eye disease: pooled analysis of two phase

Perfluorohexyloctane ophthalmic solution showed greater reductions in corneal fluorescein staining and eye dryness scores compared to a hypotonic saline control in patients with dry eye disease associated with Meibomian gland dysfunction, across various demographic and disease subgroups.

Treating meibomian gland dysfunction and glaucoma

80% of glaucoma patients on prostaglandin analogs (PGAs) have Grade 2-3 meibomian gland dysfunction (MGD), worsening ocular surface disease (OSD). Benzalkonium chloride (BAK) in chronic drops disrupts tear film stability. Symptoms like redness and tearing can lead to poor medication compliance and glaucoma progression. Innovative non-preserved or non-BAK glaucoma medications, sustained-release drug delivery systems, and non-drug treatments like selective laser trabeculoplasty (SLT) or minimally invasive glaucoma surgeries (MIGS) offer solutions. Preservative-free drops and procedural interventions aim to mitigate MGD and OSD effects.
© Copyright 2025. All Rights Reserved by MedPath