Eyenovia enrols first patient for MicroStat programme trials

27th November 2018 (Last Updated November 27th, 2018 00:00)

Eyenovia has enrolled the first patient in the first of two Phase III trials of its MicroStat programme for pharmacologic mydriasis, or dilation of the pupil for examination of eye.

Eyenovia enrols first patient for MicroStat programme trials
Pharmacologic mydriasis is essential for the standard dilated retinal fundoscopic examination. Credit: Nutschig at English Wikipedia.

Eyenovia has enrolled the first patient in a Phase III trial for its MicroStat programme studying pharmacologic mydriasis.

The safety and efficacy of Eyenovia's first-in-class fixed-combination of phenylephrine 2.5% and tropicamide 1% ophthalmic solution will be investigated as part of the MIST-1 and MIST-2 trials.

Pharmacologic mydriasis is essential for the standard dilated retinal fundoscopic examination and is said to be a key part of an estimated 80 million office-based comprehensive and diabetic eye exams performed annually in the US.

The solution will be administered as a micro-dose using the Optejet dispenser.

"We believe that our fixed-combination of phenylephrine and tropicamide has the potential to significantly improve both the patient experience and physician workflow."

Eyenovia CEO and chief medical officer Dr Sean Ianchulev said: “With the enrollment of the first patient in the first pivotal trial of MicroStat for pharmacologic mydriasis, Eyenovia officially transitions into a Phase III company.

“We believe that our fixed-combination of phenylephrine and tropicamide has the potential to significantly improve both the patient experience and physician workflow during eye exams.”

The randomised, double-blind, multi-centre Phase III trials will enrol approximately 65 participants each.

Treatment will be carried out on both eyes of participants on separate days using Eyenovia's fixed combination mydriatic solution and each of the component solutions in the MIST-1 study.

Participants will receive a fixed combination mydriatic solution and a placebo on separate days for the MIST-2 study.

Mean change in baseline pupil diameter at 35 minutes after administration of study treatment will be the primary endpoint for both studies.

Topline results from both trials are expected to be announced in the first half of next year.