ReviewDrug design, development and therapy2026
Water-Free Cyclosporine 0.1% in Dry Eye Disease: Formulation Rationale, Clinical Evidence, and Unresolved Questions.
Review in Drug design, development and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Dry eye disease (DED) is a chronic, multifactorial ocular surface disorder driven by interacting mechanisms including inflammation, tear-film instability, hyperosmolar stress, and neurosensory dysfunction. Although topical cyclosporine is an established anti-inflammatory treatment for DED, conventional formulations may be limited by poor aqueous solubility, variable ocular penetration, delayed onset of effect, and instillation discomfort. Water-free cyclosporine ophthalmic solution 0.1% was developed to address these challenges by dissolving cyclosporine in a preservative-free semifluorinated alkane vehicle, perfluorobutylpentane (F4H5), with ethanol as a formulation aid, avoiding oils, surfactants, and aqueous excipients. This review summarizes the pharmacologic rationale, preclinical evidence, clinical trial programme, safety profile, and current therapeutic role of water-free cyclosporine 0.1% in DED. Across available studies, including Phase 2, ESSENCE-1, ESSENCE-2, and a Phase 3 trial in China, treatment consistently improved objective ocular surface signs, particularly total corneal fluorescein staining, with separation from vehicle observed as early as 2 weeks in pivotal trials. In pooled ESSENCE-1 and ESSENCE-2 analyses including 1162 patients, more than 50% of treated patients achieved a clinically relevant ≥3-grade improvement in total corneal fluorescein staining after 2 weeks. A 1-year open-label extension further suggested sustained efficacy and acceptable long-term safety. In contrast, superiority over vehicle for symptom endpoints at early primary time points has been less consistent, likely reflecting symptom-sign discordance in DED, short controlled follow-up, population heterogeneity, and the lubricating properties of the vehicle. Overall, water-free cyclosporine 0.1% represents a credible addition to anti-inflammatory therapy for moderate-to-severe DED, especially when rapid improvement in corneal staining and good drop tolerability are priorities. However, the evidence base remains largely vehicle-controlled and industry-linked, with limited head-to-head comparison against other immunomodulators.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.