Neose Files IND for NE-180 for the Treatment of Anemia

Date : 06/23/2005 @ 4:38PM
Source : PR Newswire
Stock : Neose Technologies - Common Stock (MM) (NTEC)
Quote : 0.32  -0.01 (-3.03%) @ 4:01PM
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Neose Files IND for NE-180 for the Treatment of Anemia

Neose Files IND for NE-180 for the Treatment of Anemia

HORSHAM, Pa., June 23 /PRNewswire-FirstCall/ -- Neose Technologies, Inc.

(NASDAQ:NTEC) today announced that it has submitted an investigational new drug application (IND) to the U.S. Food and Drug Administration (FDA) for NE- 180. NE-180 is the company's long-acting, GlycoPEGylated erythropoietin for the treatment of chemotherapy-induced anemia. Pending clearance by the FDA, the Company expects to initiate its Phase I clinical trial in the third quarter.

About Neose Technologies, Inc.

Neose is a biopharmaceutical company using its proprietary enzymatic technologies to develop improved drugs, focusing primarily on therapeutic proteins. Neose uses its GlycoAdvance(R) and GlycoPEGylation(TM) technologies to develop improved versions of drugs with proven safety and efficacy. Neose intends to apply its technologies to products it is developing on its own and to products it co-develops and co-owns with others. It also expects to make its technologies available, through strategic partnerships, to improve the products of other parties. Neose's first two proprietary candidates are NE- 180 and GlycoPEG-GCSF, a long-acting version of granulocyte colony stimulating factor (G-CSF).

CONTACTS:

Neose Technologies, Inc.

A. Brian Davis Sr. Vice President and Chief Financial Officer (215) 315-9000

Barbara Krauter Manager, Investor Relations (215) 315-9004

For more information, please visit http://www.neose.com/.

Neose "Safe Harbor" Statement under the Private Securities Litigation Reform Act of 1995: Statements in this press release regarding our business that are not historical facts are "forward-looking statements" that involve risks and uncertainties, including without limitation the risk that we will not receive clearance from the FDA to initiate a Phase I clinical trial. For a discussion of these risks and uncertainties, any of which could cause our actual results to differ from those contained in the forward-looking statement, see the section of Neose's Annual Report on Form 10-K for the year ended December 31, 2004, entitled "Factors Affecting the Company's Prospects" and discussions of potential risks and uncertainties in Neose's subsequent filings with the SEC.

DATASOURCE: Neose Technologies, Inc.

CONTACT: A. Brian Davis, Sr. Vice President and Chief Financial Officer,

+1-215-315-9000, or Barbara Krauter, Manager, Investor Relations,

+1-215-315-9004, both of Neose Technologies, Inc.

Web site: http://www.neose.com/

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