|Nov 18, 2008
|Elite Pharmaceuticals, Inc. Hosts Quarterly Conference Call
|Northvale, New Jersey, Tuesday, November 18, 2008: Elite Pharmaceuticals, Inc. (AMEX: ELI) will host a conference call for investors and other interested parties on Wednesday, November 19th, 2008 at 11:00 a.m. ET to provide a corporate update. Topics to be discussed will include the quarterly results for period ended September 30th as well as comments on the recently completed FDA Advisory Committee meetings on opioid abuse resistant products. Company executives will also conduct a question and answer session following their remarks.
To access the conference call:Domestic callers: (800) 346-7359
International callers: (973) 528-0008
Conference Entry Code: 678890
A digital telephone replay will be available until December 3nd, 2008 following the conclusion of the call by dialing:
Domestic callers: (800) 332-6854
International callers: (973) 528-0005
Conference entry code: 678890
About Elite Pharmaceuticals, Inc.
Elite Pharmaceuticals, Inc. develops oral sustained and controlled release products. The Company's strategy includes assisting partner companies in the life cycle management of products to improve off-patent drug products and developing generic versions of controlled release drug products with high barriers to entry. Two of the company’s products, Lodrane 24® and Lodrane 24D®, are marketed by a partner, ECR Pharmaceuticals, for allergy treatment. The company’s lead pipeline products are novel sustained release oral formulations of oxycodone for the treatment of chronic pain, which address two of the limitations of existing oral opioids: the provision of consistent relief of baseline pain levels and deterrence of potential abuse. Both products, ELI-216, a once-daily abuse resistant oxycodone, and ELI-154, a once-daily oxycodone, are in late-stage development. Elite, with partners, also has an ANDA filed with the FDA for a generic equivalent of a narcotic analgesic drug product and a generic gastrointestinal drug product in clinical development. Elite operates a GMP and DEA registered facility for research, development, and manufacturing located in Northvale, NJ.
For Elite Pharmaceuticals, Inc.
Dianne Will, Investor Relations, 518-398-6222
This news release contains forward-looking statements, including those related to the preliminary nature of the clinical program results and the potential for further product development, that involve known and unknown risks, delays, uncertainties and other factors not under the control of the Company, which may cause actual results, performance or achievements of the companies to be materially different from the results, performance or other expectations implied by these forward-looking statements. In particular, because substantial future testing will be required prior to approval, the results described above may not be supported by additional data or by the results of subsequent trials. These risks and other factors, including the timing or results of pending and future clinical trials, regulatory reviews and approvals by the Food and Drug Administration and other regulatory authorities, and intellectual property protections and defenses, are discussed in Elite's filings with the Securities and Exchange Commission such as the 10K, 10Q and 8K reports. The Company undertakes no obligation to update any forward-looking statements.