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January 16, 2015
Volume 20, Number 03
Argus II approved in Canada
Health Canada has granted regulatory approval for the Argus II (Second Sight Medical Products, Sylmar, Calif.) to treat individuals with severe to profound outer retinal degeneration, Second Sight said in a press release. Argus II is the first approved retinal prosthesis in the world. The system induces visual perception in blind individuals by providing electrical pulses to stimulate the retina's remaining cells, resulting in a perception of light patterns in the brain, according to the company.
Catalys system now mobile
ForTec Medical (Streetsboro, Ohio) will bring femtosecond laser technology to practices via a mobile platform, the company announced. ForTec will bring the Catalys system (Abbott Medical Optics, Abbott Park, Ill.) to practices throughout the U.S., the company said.
RetroSense raises $6 million
RetroSense Therapeutics (Ann Arbor, Mich.) has secured $6 million in Series A financing to further investigate the use of gene therapy and optogenetics to restore vision loss, the company said in a press release. The company will use the money to complete its Investigational New Drug (IND) filing with the U.S. Food and Drug Administration for RST-001, a first-in-class gene therapy for the treatment of retinitis pigmentosa.
Allegro, Hanmi ink deal

Allegro Ophthalmics (San Juan Capistrano, Calif.) has licensed its integrin peptide therapy to Hanmi Pharmaceutical (Seoul, Korea), the companies announced in a joint press release.

Luminate (ALG-1001), a first-in-class integrin peptide therapy, is currently in phase 2 studies in the U.S., the Republic of Korea, and China for the treatment of vitreoretinal diseases. Under terms of the deal, Hanmi will pay upfront license fees, sales milestone payments, and running royalties, and will make a $20 million "strategic investment" in Allegro in exchange for license rights in Korea and China.
AAO president begins term
Russell N. Van Gelder, MD, has begun his term as president of the American Academy of Ophthalmology (San Francisco). Dr. Van Gelder is currently the chairman of the University of Washington Department of Ophthalmology in Seattle, director of the school's Medicine Eye Institute, and holds the Boyd K. Bucey Memorial Endowed chair.
Ohr names Jason Slakter, MD, to board
Ohr Pharmaceutical (New York) has named Jason Slakter, MD, chief medical officer to the company's board of directors, Ohr announced. Dr. Slakter is clinical professor of ophthalmology at New York University School of Medicine and has a clinical practice at the Vitreous-Retina-Macula Consultants of New York.
Imprimis to launch LessDrops

Imprimis Pharmaceutical (San Diego) will introduce proprietary triamcinolone acetonide and moxifloxacin hydrochloride (Tri-Moxi) and prednisolone acetate and moxifloxacin hydrochloride (Pred-Moxi) combination eye drop formulations for patients following laser refractive surgery, including LASIK and photorefractive keratectomy (PRK) surgery, cataract, and other ocular surgeries, according to a company news release.

Marketed as LessDrops, the formulations are optimized for isotonicity and may be eligible for reimbursement, Imprimis said.
Correction
An IND was submitted in January 2014 by Kala Pharmaceuticals (Waltham, Mass.), not January 2015, as published. Currently, Kala is awaiting trial results that will be published at a later date.

RESEARCH BRIEFS

  • Although vitamin D and D3 are biomarkers for time spent outdoors, there is no evidence they are associated with future myopia in children, according to a recent study. Jeremy A. Guggenheim and colleagues analyzed data from the Avon Longitudinal Study of Parents and Children (ALSPAC), a population-based birth cohort, to determine if vitamin D levels played a role in future myopia. They conducted survival analyses on 3,677 children until the children reached 15 years of age. Amount of time spent outside was measured at ages 8 and 9. Serum vitamin D2 and D3 levels were measured at age 10. More time spent outdoors resulted in higher vitamin D and D3 levels, but not vitamin D2 levels (P=0.23). There was no statistical evidence to support that the children's serum vitamin D3 levels were associated with future myopia. This study is published in Investigative Ophthalmology & Visual Science.
  • Corneal collagen crosslinking (CXL) proved effective in treating and achieving long-term stabilization of progressive keratoconus, reducing the need for corneal transplantation, according to Frederik Raiskup, MD, and colleagues. They conducted a retrospective interventional case series to analyze the 10-year results of 24 patients (34 eyes; mean age, 28.4 years±20.1 months) who underwent CXL for keratoconus between 2000 and 2004. Corneal collagen crosslinking was performed by applying riboflavin and ultraviolet-A. Corrected distance visual acuity (CDVA), corneal topography, and endothelial cell counts (ECC) were recorded preoperatively and 10 years later. The mean apical keratometry value was 61.5 D preoperatively and 55.3 D 10 years later, a statistically significant decrease (P<.001). Pre- and postoperative CDVA were also statistically significantly different (P=.002). The mean CDVA improved postoperatively by 0.14 logMAR (P=.002). The ECC remained unchanged. This study is published in the Journal of Cataract & Refractive Surgery.
  • The incidence of ocular hypertension after penetrating keratoplasty (PKP) is high, affecting almost half the patients undergoing the procedure, according to a study. Faik Oruçoglu, MD, and colleagues retrospectively reviewed hospital charts of 146 eyes that had undergone PKP between 2001 and 2003. After surgery, 70 eyes (47.9%) had at least 1 period of ocular hypertension, with a mean intraocular pressure (IOP) of 27.15±5.66 mm Hg. Ocular hypertension appeared after a mean postoperative period of 70.3±15.8 days, and continued for an average period of 15.6±2.0 days. In 35 eyes (23.9%), a second episode of IOP elevation was noted 212.2±46.8 days after the surgery. Logistic regression analysis revealed that preexisting glaucoma (P=0.009) and an additional surgical procedure combined with PKP (P=0.007) were the main factors predicting ocular hypertension after PKP. In 11 eyes (7.53%) the topical pressure-lowering therapy failed, and they required glaucoma filtering surgery. The study is published in the Journal of Glaucoma.

NEW PRODUCT BRIEFS

  • NovaBay Pharmaceuticals (Emeryville, Calif.) has rebranded its daily surfactant lid cleaner iLid Cleanser as Avenova, the company said.


EyeWorld Weekly Update is edited by Stacy Majewicz and Michelle Dalton.

 

EyeWorld Weekly Update (ISSN 1089-0319), a digital publication of the American Society of Cataract and Refractive Surgery and the American Society of Ophthalmic Administrators, is published every Friday, distributed by email, and posted live on Friday.

 

 

Medical Editors: David F. Chang, MD, chief medical editor; Bonnie An Henderson, MD, cataract editor; Clara C. Chan, MD, cornea editor; Reay H. Brown, MD, glaucoma editor; Eric D. Donnenfeld, MD, refractive editor; and John A. Vukich, MD, international editor

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