pSivida CEO to Speak at Glaucoma & Retinopathies 2010 Conference in London
Press Release Source: pSivida Corp. On Tuesday June 15, 2010, 10:00 am
WATERTOWN, Mass.--(BUSINESS WIRE)--pSivida Corp. (NASDAQ:PSDV - News)(ASX:PVA - News), a leader in the development of sustained release back of the eye drug delivery systems for difficult-to-treat conditions, today announced that its president and CEO, Dr. Paul Ashton, will be a speaker at the upcoming Glaucoma & Retinopathies 2010 conference. The conference will take place in London June 21 and 22.
Dr. Ashton will join speakers from companies that include Pfizer, GlaxoSmithKline, Allergan, Bausch & Lomb, NicOx, Neurotech, Quark Pharmaceuticals, Fovea Pharmaceuticals (Sanofi Group) and academics from University of Iceland, University of Oxford and University College London to discuss the growing area of research and clinical developments in the field.
Dr. Ashton’s presentation will focus on neuroprotection as a therapeutic target for Diabetic retinopathy and glaucoma. pSivida recently announced that two poster presentations made at ARVO reported successful pre-clinical results with the use of pSivida’s Durasert™ technology in this area.
Conference planners note that as the population ages and the incidence of diabetes rises, glaucoma and retinal disease markets may double by 2020. According to Visiongain (2010), World Ophthalmic Pharmaceutical Market 2010-2025, it is expected that these markets will remain the largest and fastest-growing areas of the ophthalmic pharmaceuticals market, with combined worldwide revenues of $20 billion by 2025. (Visiongain sponsors this annual conference).
pSivida is the first company to develop an FDA approved sustained release drug delivery system implanted in the back of the eye to deliver tiny amounts of drug on a sustained basis directly to where it would be most effective for treatment. It has developed and licensed two of the only three FDA-approved sustained release drug delivery systems (Vitrasert® and Retisert®) marketed today for treatment of back-of-the-eye conditions. It has also developed a next generation system which is licensed for use with a corticosteroid to Alimera Sciences. Alimera has announced it intends to file an NDA with the FDA this month for this system, known as Iluvien®, as a treatment for diabetic macular edema. pSivida continues to improve its technologies and focus on eye conditions with large markets and inadequate treatments that have the potential to be effectively treated using its delivery systems. pSivida’s patented technologies may also translate to other areas of the body where precise amounts of drug are required to be delivered directly to an area for optimal therapeutic benefit.
About pSivida Corp.
pSivida Corp is a world leader in the development of tiny, sustained release, drug delivery products that are administered by implantation, insertion or injection. The Company uses these systems to develop treatments for serious, unmet, medical needs. The Company’s lead development product, Iluvien, delivers fluocinolone acetonide (FA) for the treatment of DME. DME affects approximately one million people in the US and is one of the leading causes of vision loss. Currently, there are no FDA approved drugs for this disease. Iluvien, formerly known as Medidur™ FA for DME, is licensed to Alimera Sciences, which is conducting fully-recruited Phase III clinical trials and has announced that it intends to file an NDA with the FDA in the second quarter of 2010. pSivida also has two products approved by the FDA: Retisert® for the treatment of posterior uveitis and Vitrasert® for the treatment of AIDS-related cytomegalovirus (CMV) retinitis. pSivida has licensed both of these products and the technologies underlying them to Bausch & Lomb Incorporated. pSivida has a worldwide collaborative research and license agreement with Pfizer under which Pfizer may develop additional ophthalmic products. In addition pSivida has a multiple of other products in development.
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