pSivida Corp Announces First Quarter 2014 Financial Results Release Date and
Conference Call Information
WATERTOWN, Mass. -- November 5, 2013
pSivida Corp. (NASDAQ: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 first quarter of fiscal
year 2014 will be released after the market close on Tuesday, November 12,
2013, 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) 312-7507 from the U.S.
and Canada, or (631) 813-4828 from international locations. A live webcast
will be available on the Investor Relations section of the corporate website
A replay of the call will be available beginning November 12, 2013 at
approximately 7:30 p.m. ET and ending on November 19, 2013. 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: 97230646. A
replay of the webcast will also be available on the corporate website during
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™, including Tethadur™. The injectable, sustained
release micro-insert ILUVIEN® for the treatment of chronic Diabetic Macula
Edema (DME) considered insufficiently responsive to available therapies,
licensed to Alimera Sciences, Inc., is marketed in the U.K. and Germany and
has also received marketing authorization in Austria, France, Portugal, and
Spain and is awaiting authorization in Italy. pSivida has instituted the first
of two planned pivotal Phase III clinical trials for Medidur™ for the
treatment of posterior uveitis, a chronic back-of-the-eye disease. An
investigator-sponsored clinical trial is ongoing for an injectable,
bioerodible micro-insert to treat glaucoma and ocular hypertension, a product
candidate on which Pfizer Inc. has an option. pSivida's FDA-approved
Retisert®, licensed to Bausch & Lomb Incorporated, provides long-term,
sustained drug delivery to treat posterior uveitis.
Follow pSivida on social media:
The President's Blog: http://www.thechairmansblog.com/paul-ashton
For more information on pSivida, visit www.psivida.com.
Martin E. Janis & Company, Inc.
Tel: +1 (312) 943 1123
Vice President, Investor Relations
+61 (0) 41 228 1780
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