pSivida Corp. Announces Fourth Quarter and Fiscal Year 2012 Financial Results Release Date and Confe

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pSivida Corp. Announces Fourth Quarter and Fiscal Year 2012 Financial Results Release Date and Conference Call Information

WATERTOWN, Mass.--(BUSINESS WIRE)-- pSivida Corp. (NAS: PSDV) (ASX:PVA), a leader in developing sustained release, drug delivery products for treatment of back-of-the-eye diseases, today announced that its financial results for the fourth quarter and fiscal year 2012 will be released after the market close on Monday, September 24, 2012, followed the same day by a conference call and live webcast scheduled for 4:30 p.m. ET.

The conference call may be accessed by dialing (877) 303-6316 from the U.S. and Canada, or (650) 521-5176 from international locations. A live webcast will be available on the Investor Relations section of the corporate website at http://www.psivida.com.


A replay of the call will be available beginning September 24, 2012 at approximately 7:30 p.m. ET and ending on October 8, 2012. The replay may be accessed by dialing (855) 859-2056 within the U.S. and Canada or (404) 537-3406 from international locations, Conference ID Number: 32250064. A replay of the webcast will also be available on the corporate website during that time.

About pSivida Corp.

pSivida Corp., headquartered in Watertown, MA, develops tiny, sustained release, drug delivery products designed to deliver drugs at a controlled and steady rate for months or years. pSivida is currently focused on treatment of chronic diseases of the back of the eye utilizing its core technology systems, Durasert™ and BioSilicon™. The injectable, sustained release micro-insert ILUVIEN® for the treatment of chronic Diabetic Macular Edema (DME), licensed to Alimera Sciences, Inc., has received marketing authorization in Austria, France, Germany, Portugal and the U.K. and is awaiting authorization in Italy and Spain. The United States Food and Drug Administration (FDA) has cleared pSivida's Investigational New Drug application (IND) to treat posterior uveitis with the same micro-insert. An investigator-sponsored clinical trial is ongoing for an injectable, bioerodible insert to treat glaucoma and ocular hypertension. pSivida's two FDA-approved products, Retisert® and Vitrasert®, are implants that provide long-term, sustained drug delivery to treat two other chronic diseases of the retina.

For more information on pSivida, visit www.psivida.com.



In US:
Martin E. Janis & Company, Inc.
Beverly Jedynak, President, +1 (312) 943 1123
bjedynak@janispr.com
or
In Australia:
pSivida Corp.
Brian Leedman, Vice President, Investor Relations, +61 (0) 41 228 1780
brianl@psivida.com

KEYWORDS:   Australia  United States  North America  Australia/Oceania  Massachusetts

INDUSTRY KEYWORDS:

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