DSP Visulex

Clinical Validation of Noninvasive Ocular Therapeutics Administration

Aciont recently has completed a phase 1/2, multicenter, double-masked, active controlled, clinical study under a US IND filing for the treatment of noninfectious, anterior uveitis with Visulex-P combined with a proprietary formulation of dexamethasone sodium phosphate (DSP-Visulex). This clinical study examined the DSP-Visulex treatment in patients with noninfectious anterior uveitis over a period of 4 weeks. The study shows that 4 to 5 doses of DSP-Visulex therapy provides similar efficacy as the standard treatment for this indication (i.e., 112 eye drops of prednisolone acetate). Although some side effects were reported, DSP-Visulex was determined to be safe and well tolerated in this study.  Our findings will be presented at the ARVO 2018 Annual Meeting in Honolulu, HI.

Our Recent Work

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Aciont Presented at the AAO OIS in New Orleans

John Higuchi presented Aciont's DSP Visulex technology preclinical and clinical results to date at the American Academy of Ophthalmology business conference.

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Visulex-P Passive Ocular Application Treatment

This video demonstrates the activation of the DSP-Visulex proprietary drug solution with the Visulex-P drug applicator.