SAN MATEO, Calif., Oct. 29 /PRNewswire-FirstCall/ -- NeurogesX, Inc. (Nasdaq: NGSX), a biopharmaceutical company focused on developing and commercializing novel pain management therapies, today announced it will report results for its third quarter 2008 on Thursday, November 6, 2008, after the market closes.
A conference call to review the results and discuss corporate and clinical initiatives for the remainder of 2008 and into 2009 will begin at 4:30 p.m. ET (1:30 p.m. PT) on November 6, 2008 and will be hosted by Anthony DiTonno, President and Chief Executive Officer, and Stephen Ghiglieri, Chief Financial Officer.
To participate in the conference call, please dial 1-877-407-0789 (USA) or 1-201-689-8562 (International). In addition, a dial-up replay of the conference call will be available beginning November 6, 2008 at 8:00 p.m. ET (5:00 p.m. PT) and ending on November 16, 2008. The replay telephone number is 1-877-660-6853 (USA) or 1-201-612-7415 (International), Account Number: 3055, Conference ID Number: 301804.
A live web cast of the call will also be available from the Investor Relations section on the corporate web site at http://www.neurogesx.com. A web cast replay can be accessed on the corporate web site beginning November 6, 2008 at the same time as the conference call and will remain on the site for one month ending December 6, 2008.
About NeurogesX, Inc.
NeurogesX (Nasdaq: NGSX) is a biopharmaceutical company focused on developing and commercializing novel pain management therapies. Its initial focus is on chronic peripheral neuropathic pain, including postherpetic neuralgia (PHN), painful HIV-distal sensory polyneuropathy (HIV-DSP) and painful diabetic neuropathy (PDN). NeurogesX' late stage product portfolio is led by its product candidate NGX-4010, a dermal patch designed to manage pain associated with peripheral neuropathic pain conditions, that the Company believes offers significant advantages over other pain therapies. NeurogesX submitted a new drug application (NDA) for NGX-4010 with the U.S. Food and Drug Administration (FDA) in October 2008 for PHN, which is subject to acceptance by the FDA. Additionally, a marketing authorization application (MAA) for NGX-4010 seeking approval for peripheral neuropathic pain is currently under review by the European Medicines Agency (EMEA). NeurogesX' second most advanced product candidate, NGX-1998, is a topically applied, liquid formulation containing a high concentration of capsaicin designed to treat pain associated with neuropathic pain conditions. NGX-1998 is currently in a Phase 1 clinical trial. The objective of the development program for NGX-1998 is to determine its ability to provide protracted pain relief from a single treatment. As a liquid, NGX-1998 is expected to be suitable for areas of the skin where dermal patches may be difficult or impractical to apply, such as the hairline. NGX-1998 is being developed with the goal of it becoming a product that has the potential to be used by a broad spectrum of the physician population. NGX-1998 was previously studied in two Phase 1 studies in healthy volunteers conducted under an exploratory investigational new drug application.
Safe Harbor Statement
This press release contains forward-looking statements for purposes of
the Private Securities Litigation Reform Act of 1995 (the "Act"). NeurogesX
disclaims any intent or obligation to update these forward-looking
statements, and claims the protection of the Safe Harbor for
forward-looking statements contained in the Act. Examples of such
statements include, but are not limited to, possible approval of NeurogesX'
product candidates by the FDA or EMEA, the potential markets for NeurogesX'
product candidates and the expected benefits of NeurogesX' product
candidates; the suitability of NGX-1998 for certain treatments and
potential usage by broader physician populations. Such statements are based
on management's current expectations, but actual results may differ
materially due to various risks and uncertainties, including, but not
limited to, NeurogesX' product candidates may have unexpected adverse side
effects or inadequate therapeutic efficacy; positive results in clinical
trials may not be sufficient to obtain FDA or European regulatory approval;
any regulatory approvals which are received may be limited to certain
indications; physician or patient reluctance to use NGX-4010 or NGX-1998,
if approved, or the inability of physicians to obtain sufficient
reimbursement for such procedures; potential alternative therapies;
maintaining adequate patent or trade secret protection without violating
the intellectual property rights of others; and other difficulties or
delays in, clinical development, obtaining regulatory approval, market
acceptance and commercialization of NeurogesX' product candidates and the
advantages of NeurogesX' product candidates over other pain therapies. For
further information regarding these and other risks related to NeurogesX'
business, investors should consult NeurogesX' filings with the Securities
and Exchange Commission.
Chief Financial Officer
The Ruth Group
Stephanie Carrington / Sara Ephraim (investors)
(646) 536-7017 / 7002
Jason Rando (media)
|SOURCE NeurogesX, Inc.|
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