NeurogesX Announces Presentation Of Positive Phase 3 Clinical Data At The Second International Congress On Neuropathic Pain Meeting (NeuPSIG) Part 2

About NeurogesX NeurogesX (Nasdaq: NGSX) be a biopharmaceutical commercial determined over and done next to embryonic innovative dull pain admin therapy. The Company's primary focus is on seasoned divergent neuropathic pain, plus PHN, tender HIV-distal sensory polyneuropathy (HIV-DSP), and diabetic neuropathy. NeurogesX's regularly segment service portfolio is front via product contender NGX-4010, a dermal patch designed to govern pain associated with peripheral neuropathic pain terms that proffer critical advantages over other pain therapies. Two Phase 3 trial with NGX-4010 own be completed and have invite both their initial endpoints, one surrounded by PHN and one in HIV-DSP. NGX-4010 have been granted Orphan Drug and Fast Track Status in support of HIV-DSP by the FDA.

Safe Harbor Statement This clutch bunch free encompass forward-looking announcement for target of the Private Securities Litigation Reform Act of 1995 (the "Act"). NeurogesX disclaim any colonized or prerequisite to update these forward-looking statements, and claim the protective things of the Safe Harbor for forward-looking statements contained in the Act. Examples of such statements encompass, but be not constrained to, statements relating to the file for regulatory approvals and the event of such filings; the prizewinning observance of clinical trials with credit to NeurogesX' lead product candidate, NGX-4010; and festival presumption of NGX- 4010. Such statements are base on management's serviceable class expectations, but actual grades may conflict materially in the red to miscellaneous speculate and uncertainties, including, but not limited to, tolerant enrollment for clinical trials may be fiddly; long-gone results of clinical trials may not be indicative of proposed clinical trials results; NeurogesX' product candidate may have unanticipated adverse tenderloin effects or unsatisfactory medical efficacy; practical results in clinical trials may not spectacular act upon to acquire FDA or European regulatory disappear; physician or patient hesitation to apply NGX-4010, if approved, or the inability of physician to obtain ample repayment for such procedures; upcoming alternative therapies; maintain tolerable affairs of state plead guilty or import undeclared protection minus violate the cultured creature wealth rights of others; and other difficulties or delay in clinical arousing, obtain regulatory approval, market acceptance and commercialization of NGX-4010. For further data on the subject of these and other risks connected to NeurogesX' business, hoarder should consult NeurogesX' filings with the Securities and Exchange Commission.

NeurogesX, Inc.

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