SAN DIEGO, March 18, 2013 (GLOBE NEWSWIRE) -- Apricus Biosciences, Inc. ("Apricus Bio" or the "Company") (Nasdaq:APRI) ( http://www.apricusbio.com ), today provided an update regarding ongoing corporate activities and announced that its Annual Report on Form 10-K for the quarter and year ended December 31, 2012 has been filed with the Securities and Exchange Commission earlier today. As previously announced, the Company will host its fourth quarter and year end 2012 financial results conference call today, March 18, 2013 at 1:00 PM ET.
- Announced new corporate strategy focused on Vitaros® and Femprox®. In January 2013, Apricus Bio announced its corporate goals for 2013, which includes focusing its corporate strategy and resources on commercializing its lead product Vitaros® (alprostadil 0.3% topical cream), for the treatment of erectile dysfunction ("ED"), and on further developing through clinical trials its lead product candidate, Femprox® (alprostadil 0.4% topical cream), for the treatment of female sexual arousal disorder ("FSAD"). Both products utilize Apricus Bio's proprietary NexACT® transdermal delivery platform.
- Ceasing of funding of French Subsidiaries. In March 2013, Apricus Bio announced that, as part of its effort to focus resources on its lead assets, it intends to cease financing its French subsidiaries, Finesco SAS, Scomedica SAS and NexMed Pharma SAS. The strategic decision to cease financing its French subsidiaries follows a decrease in the unit's operating performance resulting from recently enacted pricing policies affecting drug reimbursement in France and the subsequent, related loss of certain contract sales agreements.
- Divestiture of oncology supportive care business. In January 2013, Apricus Bio announced its plans to seek a buyer for its oncology supportive care products, which include the rights to Totect® (dexrazoxane for injection) for the treatment for extravasation from intravenous anthracycline chemotherapy in the U.S. and the Americas, and the U.S. co-promotion rights to Granisol® (granisetron HCl oral solution) for the prevention of nausea and vomiting associated with certain emetogenic cancer therapies and radiation. Each of these products is now commercially available and marketed in the U.S. The planned divestiture will allow Apricus Bio to better align its resources with its stated corporate objectives.
- Commercial Launch of Vitaros® in Canada through Abbott Laboratories. Apricus Bio is actively supporting Abbott with their pre-launch efforts, and continues to expect that a full launch will occur in the first half of 2013.
- European approval decision for Vitaros® in Europe via the Decentralized Procedure ("DCP"). A decision regarding the approval of Vitaros ® in Europe via the DCP with Netherlands as the Reference Member State is expected to occur in the first half of 2013, followed by national phase approvals in each of the major markets of Europe. Marketing of Vitaros ® can then be initiated in each country by Apricus Bio's commercialization partners. In Europe, existing ED products currently generate over $1 billion dollar in sales and Apricus Bio believes a significant portion of the market remains untreated or undertreated.
- Obtain feedback from regulatory agencies and initiate next clinical steps for Femprox®. In 2013, Apricus Bio expects to announce feedback from its meetings with Health Canada and the U.S. FDA, as well as its plan for Femprox ® clinical development going forward.
- Secure additional Vitaros® partnerships. Vitaros ® is now partnered in key markets around the world, including the U.S., Canada, Germany, the United Kingdom, Italy, the Gulf countries, certain other countries in the Middle East and Israel. The Company is looking to secure partnerships in the remaining major global markets.