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2021 Canadian ECP Myopia Study results now available

2021 Myopia Report available

The 2021 Myopia study final report of Canadian ECPs attitudes is now available

The purpose of the Canadian Myopia Management ECP study is to characterize the attitudes toward myopia management and use of the various therapies. 

The initial study, conducted in 2019, revealed the extent to which Canadian ECPs were engaged in myopia control and the extent to which the various clinical treatment options were used.

The study also measured the perception of efficacy for each of the major therapeutic categories.

In the last 18 months,  several new myopia treatment options have been made available in the Canadian market and there has been a significant increase in related marketing activity and practitioner education. 

“This important study indicates how new treatment options are impacting perceptions of efficacy and overall attitudes toward the condition. Also interesting to note, is the significant impact that education has had within the practitioner community over the 18 months since our last report”, said Bill Scott, President, Optical Research, ECP & PAA of the Jobson Optical Group. 

The 2021 study, which is now available, reveals notable changes in usages of the different treatments and changes in perception of efficacy.  

The 2021 report also includes the onset age of treatment by therapeutic type, and the extent to which axial measurement equipment is utilized as a diagnostic tool. 

The 2019 study revealed a significant proportion of ECPs were skeptical of the clinical significance of myopia as a serious eye disease. The current 2021 report updates these perceptions against the background of extensive practitioner education over the past 18 months and more specific treatment options available.

Final Survey report is now available

The 2021 report draws out salient attitudinal differences compared to 2019.

Final Report now available
The online study was jointly conducted by Jobson Research and VuePoint IDS. 

Organizations wishing to purchase the study report may do so by contacting:
David Pietrobon (dpietrobon@vuepoint.ca)   Phone:   226.780.6871 x 5111
Bill Scott (Bscott@jobson.com)    Phone:   646.831.8873

FYidoctors Doubles Retail Offering in Hometown Grande Prairie

FYidoctors announces the addition of its second location in Grande Prairie, Alberta. The newly constructed clinic, which is located on Westgate Drive, marks a significant milestone for the organization, whose entrepreneurial success story began 13 years ago in the growing community. The inaugural location remains its largest clinic in Canada. 

“We’re incredibly proud to announce the opening of our second clinic in Grande Prairie, a region long regarded as a foundational part of our history,” said Dr. Alan Ulsifer, CEO and Chairman of FYidoctors. “Our roots are here, and we couldn’t be more thankful to the community that contributed to the success of FYidoctors.”

The new location adds clinic leads Dr. Michael Litchfield and Dr. Joel Heath, both of whom are active members in the Grande Prairie community, having first worked at the FYidoctors location on 99th Street.

“We’re pleased to announce the new addition, which helps meet the growth and vision care needs of Grande Prairie and its surrounding communities,” said Dr. Heath. “As an organization who prides itself in taking a doctor-led, comprehensive approach to vision care, we’re thrilled to add a second location, and to provide new and existing patients with the most current eye care technology available, with the added care and benefits available through FYidoctors,” added Dr. Litchfield.

As part of the grand opening celebrations, on October 1st, 2021, the FYidoctors Westgate clinic hosted an official ribbon-cutting ceremony alongside the Grande Prairie & District Chamber of Commerce.
 

Click HERE for the full press release.

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CRAVING MIDO: Ready to Restart and to Transform the Wonder into a New Beginning

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Starting today, on the MIDO website www.mido.com, visitors to the international eyewear show ‒ buyers, designers, entrepreneurs, opticians, ophthalmologists and eyewear supply chain professionals ‒ can register for the forthcoming edition of the show, set to take place February 12-14, 2022.

The premier global B2B eyewear show is coming back, with in-person participation in complete safety at Fiera Milano Rho, for a not-to-be-missed industry event.
New trends, materials, sustainability, innovation and the future will be the foremost topics of interest.  

The 2022 edition will be distinctive and unforgettable: There will be encounters with distinguished guests, awards, honors and previews in the pursuit of “craving a new beginning”. The event will also be complemented by the MIDO 2022 I DIGITAL EDITION, the digital platform launched in June 2021 that helps boost a beneficial connection between the physical and digital worlds.

The craving for renewal and creativity begins with the new 2022 campaign ‒ dynamic, interactive and in real time, complete with augmented reality, employed for the first time by an eyewear trade show ‒ based on the “CRAVING MIDO” claim. It is divided into 4 volumes. Just scan the QR code to view the star players and their stories.

“We crave a restart and we want to do it looking each other in the eyes,” exclaimed President Giovanni Vitaloni. “We want to rebuild, innovate, demonstrate what we are made of – to forge new relationships, strengthen existing ones and get back to making our businesses prosper. First half data on industry performance raised our hopes for the future but we are even more impressed by the robust participation in industry trade shows that are finally popping up in various markets, like DaTE, where the spirit of recovery was in the air,” he concluded.

Click HERE for the full press release.

Bausch + Lomb Announces Statistically Significant Topline Results from Second Phase 3 Trial of NOV03

Bausch + Lomb and Novaliq announced statistically significant topline data from the second Phase 3 (MOJAVE) trial evaluating the investigational drug NOV03 (perfluorohexyloctane) as a first-in-class eye drop with a novel mechanism of action to treat the signs and symptoms of dry eye disease (DED) associated with Meibomian gland dysfunction (MGD). The companies announced statistically significant topline data from the first Phase 3 trial (GOBI trial) in April 2021.

“The findings from this second Phase 3 trial reinforce the results of the first Phase 3 trial and further supports the efficacy and safety profile of NOV03 as a potential important new treatment option for the millions of people living with dry eye disease associated with MGD,” said Joseph C. Papa, chairman and CEO, Bausch Health. “These results mark another important milestone in bringing NOV03 to market as a potential first-in-class treatment, and we anticipate filing a New Drug Application to the U.S. Food and Drug Administration in 2022.”

The MOJAVE trial met both primary sign and symptom endpoints, and also met all of its secondary endpoints, showing statistically significant improvements in each of the signs and symptoms of DED associated with MGD that were evaluated.

“We are extremely pleased by the consistency of the results, which reaffirm the safety and efficacy results for this investigational drug previously demonstrated in a Phase 2 trial and the first Phase 3 trial. This underscores the potential impact NOV03 could have, if approved, in addressing an unmet medical need for the millions of patients with dry eye disease associated with MGD,” said Christian Roesky, Ph.D., CEO, Novaliq.

The clinical development program for NOV03 is expected to conclude with an ongoing multi-center, open-label, single-arm, 12-month safety extension trial (KALAHARI).

Click HERE for the full press release.

Related:

Bausch + Lomb Announces Results from First Phase 3 Trial of NOV03

CooperVision: SightGlass Vision Diffusion Optics Technology Demonstrates Significant Reduction in Myopia Progression

CooperVision’s SightGlass Vision Business has revealed two-year clinical study data for its Diffusion Optics Technology, which is specifically designed to slow the progression of myopia in children. After two years, children who wore their Diffusion Optics Technology-enabled spectacles full time, including not removing them for near vision activities, progressed on average one-half diopter less than those wearing the control spectacles—a reduction of 59%.

The news was presented during a launch event in the Netherlands yesterday, timed with the world’s first commercial launch of the technology. The product will be available from CooperVision to eye care professionals in the Netherlands beginning this month. EssilorLuxottica, which will also introduce the spectacle lenses with Diffusion Optics Technology, participated as well.

The CYPRESS clinical study enrolled, randomized, and dispensed the lenses to 256 eligible children across 14 clinical trial sites in the United States and Canada. At the time of enrollment, subjects were 6 to 10 years old having myopia between -0.75 D and -4.50 D.

After two years of wear, 85% of children wearing the innovative spectacle lenses showed less than one diopter of myopia progression. Moreover, the study also showed that 41% of the children wearing spectacle lenses with Diffusion Optics Technology showed no clinically meaningful progression in refractive error after two years versus only 17% in the control group.

Distance visual acuity with lenses incorporating Diffusion Optics Technology was on average better than 6/6 (20/20) at each visit and similar to single vision spectacle lenses at all visits from dispensing through the 24-month visit. In the trial, children on average wore both the test lenses and standard single vision spectacle lenses more than 12 hours each day over a 24-month period, suggesting that children readily adapted to the Diffusion Optics Technology. The CYPRESS trial is now continuing into its third year.

“Our team has been singularly focused on advancing medical science to not only correct children’s vision, but also to help slow the progression of myopia. Applying our Diffusion Optics Technology to spectacle lenses makes myopia management straightforward to integrate within eye care practices and easy to become part of children’s everyday lives,”8 said Joe Rappon, OD, MS, FAAO, chief medical officer for SightGlass Vision.

Spectacle lenses incorporating SightGlass Vision Diffusion Optics Technology™ already hold a CE Mark declaration to help slow the progression of myopia.

Earlier this year, CooperCompanies and EssilorLuxottica announced their intent to form a joint venture to accelerate the commercialization of technologies from SightGlass Vision.

Click HERE for the full press release.

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