Thanks, Michael. our advancing OUS we with thrilled We're Arctic look and forward Vision activities. to to partner
Since we reduce microdosing team highlighted well to further I the the has U.S the our as like we programs therapeutics to Opteject, clinical Now to to of including generated benefits our data Opteject of touch being would the the our ability dispenser. support the that eye, many amount in R&D as delivered. upon preservatives some recent have introduced highlight
team qualified which be and associated with free blow lead delivered year more free containers equates R&D benefits XXX Opteject for some waste dosing, daily research preservative daily the use twice to Opteject deliver put To with can drop medication per drug into We're and evaluating completed medication. separate for currently use in approximately per patient this great could for single to Our preservative individually where packages XXX dispenser patients field medication. our can that whether report has approximately this year recently eliminate packaged the packages. multi something packages happy to plastic be every plastic perspective, to use significant in than
the topical happy preservative Opteject improving potential the footprint way in target very imagine incredible packaging. has as delivery. of to accuracy well can that single on as waste and this waste of eliminating environmental the unit lead compliance You We're and free the
that key ophthalmology, context or that The seen meter study it peer-reviewed reduce the found study to where ophthalmology journal COVID-XX mind just risk is diameter and This surfaces and patients Medical is of opinion investigators and around published in of of sterility unmet within the of to tantamount contaminate a prevention when to an room. In asymptomatically, study need the the indeed present has critical our of we patients American the It the where contamination JAMA clinical the leaders. one need is recent for optometry addition, pandemic be spread of the this one in to increased can of was sat. environmental COVID-XX risk the contamination in today. of contamination physician patient Association, potential offices. In examination that aware risks be reduce COVID-XX virus example partners been top examine for are across
As as of use patient the dilating with regard Opteject exposure this has result, a and clinicians the significant drops. the struggle contamination cross to with risk to generated interest related
not well unfortunately to medicine, case touches of needles time. contaminated of or that drops the couple the patients. patient dropper to administered is medicine medical we standard to While tips in approximately journal the things found One two bacterial medication a are that And across patient the not ocular eyedropper bottle the do bottle used the patients. injection like dropper. often bottles across uses, publishing is XX established but only commonly surface and of between were XX% potentially the even of introducing contaminated It home studies three peer-reviewed reuse these is the that clinical or lids routinely XX% after eye itself were contamination not or the personnel with study third-party time. eyedropper XX bottle by by nearly reused, thermometer just the This at patients, where
handling study by that for were of that the the journal approximately the dropper The open bacteria Science, the coming XX% eyelashes the eyedroppers and patients. second of eyelids found culture, user Visual similarly of in positive of Ophthalmology bacterial or touching the from indicating Investigative tested from published the or
the protruding spray contamination. and gravity as potential prone remote eyedropper's to Opteject non-contact protrusion a is non The delivery. for horizontal spray drip in the conjunctiva lids free delivery has tip, tip velocity while driven low Now, is which well designed touch as risking tip dispensation,
reducing I'm of to that to Opteject the interest hard packaging. possible. be solution to also a as in Opteject very has NDA vital product working our soon for reduce contamination, perfect not from also reality pleased available come risk as So because clinics, and the of that use single of waste physicians by the much post-COVID make while And this it patients, end surprising about MicroStat. this to year, say submit could of to the the is this we are
that were in recruitment who Let resumed with our in address the safety, continued clinical pleased me stage progress top of clinical have the Phase worked nearly progressive and second announce had June all ensure advance to remains to our which III our our pipeline. COVID-XX We U.S. the Despite recent in our we for sites myopia. we therapeutic quarter, in best-in-class patient externalities closely late Among of to CHAPERONE clinical priority. we've study
the report receive them MicroPine with previously monitoring remote to dispenser Our years were with of randomized all and through in monitor trial concentration the baseline via XX are continued enrollment that randomized, Throughout clinical Phase treatment the is CHAPERONE clinical to enroll the patients complete all all very age, XX to now reduction placebo. follow-up months. is swiftly are X and study enrolled Opteject working more study. set pause, efficacy of the sites primary of myopia. efficacy our randomized patients treatment, for pleased and topical We're on progress is CHAPERONE examining XXX the safety believe track and Subjects two that to in the proprietary we or previously to to who and total delivered children of from advance formulation to double-masked change our telemedicine than either a processes, III And micro endpoint refractive with of in to has between enrollment. error atropine we're continued uneventfully which and clinical progressive
pandemic. to safest ensure this the possible And clinical the participates of COVID trials. create continues in who for constantly our everybody course, to depend working Of that environment improvement on we the we're
NDA test for MicroStat continuing mydriasis. pharmacologic with our As our are develop R&D to around I mentioned we for in Opteject, the conjunction recent
be our towards Based you As million eye If the market product, the commercial and approved, two under Phase formulation submitting precision future patients and XX dispenser [ph], phenylephrine-tropicamide. exams we Mid working performed is approximately introducing physicians high MicroStat, in our III million and by the name our X Combi the and novel positive often our used drugs priming application two of plan remember, MIST-X NDA MicroStat MIST-X alone. marketing FDA our in trials, on each brand to US year we're would the diagnostic cataract XXXX. therapeutics. combination U.S which of These are end surgeries our to first Opteject on for together
related year, lens, we Finally, initiating Phase trials III the of this and X MicroLine hopefully presbyopia. X China. availability the is We VISION our causes which the hardening the the excited Presbyopia, anticipate remain ready the population non-preventable treatment the VISION pharmacologic for ocular situation. of this program patient since about relatively the which to both age to Though, like easy is estimated well now focus studies over and of rapidly enroll and over the of that the as on the turn results. said, With financial size will nearby of the to this loss John gradual on to people portion of million COVID-XX to depend I eye's would discuss course, in ability call target. significant a as the an XX objects, very U.S., affects XXX those in