OxectaTreatment for Pain
Update: Oxecta (oxycodone) Now FDA Approved - June 17, 2011
Update on FDA Advisory Committee Meeting For Acurox
Acura Pharmaceuticals and King Pharmaceuticals Provide Update on FDA Advisory Committee Meeting For Acurox
PALATINE, Ill. and BRISTOL, Tenn., April 22 /PRNewswire-FirstCall/ -- Acura Pharmaceuticals, Inc. today announced that the U.S. Food and Drug Administration's (FDA) Anesthetic and Life Support Drugs and Drug Safety and Risk Management Committees voted that they do not have enough evidence to support the approval of the New Drug Application (NDA) for Acurox (oxycodone HCl and niacin) Tablets for the treatment of moderate to severe pain, considering the deterrent effects of niacin as well as the potential deterrent effects of the other features specific to Acurox. The addition of niacin to Acurox was central to the deliberations. The FDA is not bound by the Advisory Committees' recommendation, but may take its advice into consideration when evaluating the NDA for Acurox Tablets. Acura and King will work with the FDA to determine the next steps for the Acurox development program.
Acurox is an investigational immediate-release product containing two active ingredients and essential functional inactive ingredients. Each Acurox tablet contains oxycodone HCl as the sole active analgesic ingredient. Niacin, the second active ingredient, is intended to minimize the potential for oral abuse of oxycodone HCl. The functional excipients are intended to provide limits and impediments to the abuse of Acurox Tablets by snorting and intravenous methods. Both oxycodone HCl and niacin are FDA-approved drugs with extensive clinical experience and well-characterized safety profiles.
About Acura Pharmaceuticals, Inc.
Acura Pharmaceuticals, Inc., is a specialty pharmaceutical company engaged in research, development and manufacture of product candidates intended to provide abuse-deterrent features and benefits utilizing the Company's proprietary Aversion Technology, Impede(TM) Technology, and other novel technologies. Acura entered into a License, Development and Commercialization Agreement with King Pharmaceuticals, Inc., in October 2009 pursuant to which Acura and King are now jointly developing Acurox Tablets and three additional opioid analgesic product candidates utilizing Aversion Technology.
About King Pharmaceuticals, Inc.
King, headquartered in Bristol, Tennessee, is a vertically integrated branded pharmaceutical company. King, an S&P 500 Index company, seeks to capitalize on opportunities in the pharmaceutical industry through the development, including through in-licensing arrangements and acquisitions, of novel branded prescription pharmaceutical products and technologies that complement the Company's focus in specialty-driven markets, particularly neuroscience and hospital. King's wholly owned subsidiary, Alpharma Inc., is also a leader in the development, registration, manufacture, and marketing of pharmaceutical products for food-producing animals.
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 (the "Act"). When used in this press release, the words "estimate," "project," "anticipate," "expect," "intend," "believe," and similar expressions are intended to identify forward-looking statements. Examples of forward-looking statements in this press release include statements concerning the Companies' expectations regarding working with the FDA. Acura Pharmaceuticals, Inc. and King Pharmaceuticals, Inc. disclaim any intent or obligation to update these forward-looking statements, and claim the protection of the Safe Harbor for forward-looking statements contained in the Act. Such forward-looking statements involve known and unknown risks, uncertainties and other factors which may cause actual results, performance or achievements to be materially different from any future results, performance, or achievements expressed or implied by such forward-looking statements. Important factors that may cause actual results to differ materially from the forward-looking statements are discussed in the "Risk Factors" section and other sections of each of the Companies' Annual Reports on Form 10-K for the fiscal year ended December 31, 2009, each of which is on file with the U.S. Securities and Exchange Commission.
IMPEDE is a trademark and ACUROX and AVERSION are registered trademarks of Acura Pharmaceuticals, Inc.
Source: King Pharmaceuticals, Inc.; Acura Pharmaceuticals, Inc.
Posted: April 2010
- Pfizer and Acura Announce FDA Approval of Oxecta (Oxycodone HCl, USP) CII - June 20, 2011
- King Pharmaceuticals and Acura Pharmaceuticals Announce Submission of New Drug Application for Acurox Tablets - December 20, 2010
- King Pharmaceuticals and Acura Pharmaceuticals Announce Plans to Submit an NDA for Acurox Tablets without Niacin - May 4, 2010
- Acura Pharmaceuticals and King Pharmaceuticals Provide Update on Acurox NDA - September 3, 2009
- Acura and King Receive FDA Complete Response Letter Regarding Acurox - July 2, 2009
- Acurox Tablets New Drug Application Accepted for Filing With a Priority Review Classification - March 3, 2009
- New Drug Application Submitted For Acurox Tablets - January 2, 2009