Wednesday, June 21, 2017| Business, Clinical Trials, Novartis, Psivida, Retina, Uveitis, Wet AMD

EyewireTV — Novartis Wet AMD Candidate Advances; New Leadership Changes

In this week’s EyewireTV, Novartis’ wet AMD candidate RTH258 (brolucizumab 6 mg) meets the primary and secondary endpoints in two phase 3 trials; and a second phase 3 trial of pSivida's Durasert 3-year treatment for posterior uveitis achieves its primary endpoint by demonstrating a significant reduction in the recurrence of posterior uveitis through 6 months. Also, several leadership changes are announced in the ophthalmology industry.

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Wednesday, June 14, 2017

EyewireTV — Eye Care Executives Discuss Recent Changes

In this week’s EyewireTV, eye care executives discuss how recent changes at their companies will improve service and access to technology for physicians and patients.

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Wednesday, June 07, 2017| Bausch+Lomb, Capsulotomy/Capsulorrhexis, Carl Zeiss Meditec, Conjunctivitis, FDA Approval/Clearance, Nicox , Valeant, ZEPTO Precision Pulse Capsulotomy

EyewireTV — Zepto Approved in US; B+L Surgical Products for Sale?

In this week’s EyewireTV, Mynosys Cellular Devices receives FDA 510(k) clearance for the Zepto Capsulotomy System; and the FDA approves Nicox’s allergic conjunctivitis drug Zerviate (cetirizine 0.24%), the first topical ocular formulation of the antihistamine cetirizine. Also, Valeant reportedly is in talks to sell its Bausch + Lomb unit’s surgical products business to Carl Zeiss Meditec.

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Wednesday, May 31, 2017| Aerie Pharmaceuticals, Beaver-Visitec International, BVI, Clinical Trials, FDA Approval/Clearance, Genentech, Glaucoma, Product Releases

EyewireTV — First FDA Approval for GCA; Phase 3 Roclatan Results

In this week’s EyewireTV, Genentech receives FDA approval for Actemra (tocilizumab) for the treatment of giant cell arteritis, marking the first FDA-approved treatment for the disease; and Aerie Pharmaceuticals reports positive phase 3 topline efficacy results for its fixed-dose combination glaucoma product candidate, Roclatan. Also, Beaver-Visitec International announces the US launch of a long-term dissolvable punctal implant—the Extend 180.

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Wednesday, May 24, 2017| American Society of Cataract & Ref Surgeons, ASCRS, Business

EyewireTV — Eye Care Executives Discuss the Future of Ophthalmology

In this week’s EyewireTV, executives at the Ophthalmology Innovation Summit in Los Angeles provide EyewireTV updates on their company’s products and pipeline.

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Wednesday, May 17, 2017| Dry Eye, Fluoroquinolones, Nidek, Retinal detachment, RD

EyewireTV — New Dry Eye Guidance; Fluoroquinolones/Retinal Detachment Link

In this week’s EyewireTV, the Tear Film & Ocular Surface Society (TFOS) presents the conclusions and recommendations of the TFOS Dry Eye Workshop II (DEWS II), which may have an impact on the way dry eye disease is diagnosed and examined; and new FDA communication indicates there is no firm evidence suggesting that fluoroquinolone antibiotics may lead to retinal detachment. Also, Nidek launches the SL-2000 Slit Lamp, which aims to provide a clear view of ocular tissue in nearly natural color.

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Wednesday, May 10, 2017

EyewireTV - Breaking Industry News from the ASCRS Meeting in Los Angeles

In this week’s EyewireTV, Bausch + Lomb introduces the Stellaris Elite vision enhancement system and Vitesse open-port vitrectomy system; and Zeiss fully integrates the latest generation of Barrett IOL power calculation formulas into the IOLMaster 700. Also, Alcon launches two new cataract surgical technologies—the Intrepid Transformer I/A Handpiece and LenSx Laser SoftFit Patient Interface options.

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Wednesday, May 03, 2017| AngioVue OCTA system, Clinical Trials, Dry Eye, Inflammation, Kala Pharmaceuticals, optical coherence tomography angiography, OCT angiography, Optovue, Parion Sciences, Shire

EyewireTV - New OCTA Imaging; Shire Acquires Rights to DED Drug Candidate

In this week’s EyewireTV, Optovue releases the AngioVueHD, an update to the AngioVue system that allows for higher-density OCT angiography imaging; and Kala Pharmaceuticals announces positive topline results from its phase 3 clinical trial of KPI-121 1% for postoperative inflammation and pain. Also, Shire and Parion Sciences enter into an agreement granting Shire exclusive global rights to develop and commercialize dry eye disease drug candidate P-321.

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Wednesday, April 26, 2017| Allergan, Clinical Trials, Diabetic Retinopathy, FDA Approval/Clearance, Hydrus™ Microstent, Ivantis, Technology

EyewireTV — FDA Clears TrueTear Neurostimulator; IBM Technology Detects DR

In this week’s EyewireTV, Allergan receives marketing authorization from the FDA for the TrueTear Intranasal Tear Neurostimulator, developed to temporarily increase tear production during neurostimulation in adult patients; and IBM releases the results of new research using deep learning and visual analytics technology to advance early detection of diabetic retinopathy. Also, Ivantis receives FDA clearance to initiate a second investigational device exemption clinical trial of the Hydrus Microstent.

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Tuesday, April 11, 2017| Bausch+Lomb, Dry Eye, FDA Approval/Clearance, Imprimis Pharmaceuticals, Phacoemulsification, Stellaris Vision Enhancement System

EyewireTV — FDA Outpaces Europe in Drug Approvals; New Phaco Platform

In this week’s EyewireTV, a study published online in the New England Journal of Medicine reveals that the FDA outpaced the European Medicines Agency in review times and approval of new drugs between 2011 and 2015; and Bausch + Lomb receives FDA 510(k) clearance for the Stellaris Elite vision enhancement system, the company’s next-generation phaco platform. Also, Imprimis Pharmaceuticals enters into a licensing agreement for the exclusive worldwide rights to Klarity, a patented ophthalmic topical solution and gel technology for patients with dry eye disease.

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Wednesday, April 05, 2017| , Cataracts

EyewireTV - Ocular Melanoma Trial; Hepatitis C Link to Cataracts

In this week’s EyewireTV, the first cases using a new drug candidate (AU-011; Aura Biosciences) for treating ocular melanoma are performed at Wills Eye Hospital in Philadelphia; the National Eye Institute outlines its Audacious Goals Initiative, which provides recommendations for regenerating retinal ganglion cells. Also, a large population-based study suggests hepatitis C infection may increase the risk of cataracts.

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Wednesday, March 29, 2017| AcrySof® IQ ReSTOR Multifocal IOL, Alcon, Allergan, Astigmatism, FDA Approval/Clearance, Intraocular Pressure, IOP, Presbyopia

EyewireTV — New Multifocal Toric IOL; Restasis Multidose Now Available

In this week’s EyewireTV, the FDA approves Alcon’s Acrysof ReSTOR 2.5 D Multifocal Toric IOL with Activefocus, designed to address astigmatism and presbyopia at the same time; and Allergan announces the availability of Restasis Multidose, the first and only FDA-approved preservative-free, prescription eye drop in the United States to be available in a multidose bottle. Also, the Icare HOME tonometer, which allows for 24-hour self-measuring of IOP, receives FDA clearance.

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Wednesday, March 22, 2017| dry age-related macular degeneration, dry AMD, Glaucoma, Glaukos Corporation, Intraocular Pressure, IOP, Microinvasive Glaucoma Surgery (MIGS), Minimally Invasive Micro Sclerostomy (MIMS) , stem cell therapy

EyewireTV — Unregulated Stem Cell Procedures; New Glaucoma Device

In this week’s EyewireTV, the New England Journal of Medicine details an alarming case in which three women with dry AMD suffered severe, permanent eye damage after stem cells were injected into their eyes in an unproven treatment at a clinic in Florida; and Israel-based Sanoculis receives the CE Mark for its minimally invasive micro sclerostomy (MIMS) device for the reduction of IOP in glaucoma patients. Also, the American Medical Association grants Glaukos 5-year extensions to three Category III CPT codes that detail Medicare reimbursements for current and future microinvasive glaucoma surgery (MIGS) devices.

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Wednesday, March 15, 2017

EyewireTV - Footage of the First SMILE Procedures; Ackman Unloads His Valeant Stock

In this week’s EyewireTV, exclusive footage of the first ReLEx SMILE procedures to be performed in the United States following the recent FDA approval; and Pershing Square Capital Management CEO Bill Ackman said that his hedge fund has sold all its shares in Valeant, the parent company of Bausch + Lomb. Also, eSight Corporation launches new electronic glasses that aim to restore up to 20/20 vision to the blind.

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Wednesday, March 08, 2017| FDA Approval/Clearance, Glaucoma, IOL Calculations, IRIDEX, Topcon Medical Systems

EyewireTV — Republicans Aim to Replace Obamacare; Aladdin Biometer FDA Clearance

In this week’s EyewireTV, House Republicans unveil legislation called the American Health Care Act, which aims to repeal and replace the Affordable Care Act; and Topcon Medical Systems receives FDA clearance for the Aladdin Biometer with Corneal Topographer HW3.0, a device designed to save time and add accuracy to IOL calculation measurements. Also, Iridex announces the availability of the G-Probe Illuminate, a new FDA-cleared probe for use with the CYCLO G6 Glaucoma Laser System.

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