Ranibizumab joins laser surgery as diabetic macular edema treatment
August 16th 2012The FDA has approved once-monthly, 0.3-mg ranibizumab injection (Lucentis, Genentech) for treatment of diabetic macular edema (DME), making it the first and only drug approved by the agency for the condition. The standard of care for DME for the past 25 years has been laser surgery.
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Uveitis insert gets OK for phase III trials
August 1st 2012The FDA has cleared pSivida Corp.’s Investigational New Drug application to treat posterior uveitis with an injectable sustained-release fluocinolone acetonide micro-insert, which releases fluocinolone acetonide at a consistent rate over a period of approximately 36 months.
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Fluocinolone acetonide implant gets German marketing approval
August 1st 2012An intravitreal implant that delivers sub-microgram levels of fluocinolone acetonide for up to 36 months (Iluvien, Alimera Sciences Inc.), has been granted marketing authorization by the Federal Ministry of Health of Germany (Bundesministerium fur Gesundheit, BfArM) for the treatment of vision impairment associated with chronic diabetic macular edema considered insufficiently responsive to available therapies.
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ASCRS task force looks at ways ophthalmologists, optometrists can collaborate
August 1st 2012The formation of a new organization to represent all eye-care practitioners is one of the possibilities being considered by a task force examining ways that ophthalmologists and optometrists can collaborate to provide patient care.
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FDA panel recommends ocriplasmin for vitreomacular adhesion
August 1st 2012Ocriplasmin (ThromboGenics) should be approved for the treatment of symptomatic vitreomacular adhesion (VMA), according to a unanimous recommendation to the FDA by its Dermatologic and Ophthalmic Drugs Advisory Committee.
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