GlycoGenesys, Inc. to Announce Clinical Data and Present at Roth Capital Partners New York Conference September 8th, 2005
31 August 2005 - 5:00AM
Business Wire
GlycoGenesys, Inc. (NASDAQ:GLGS), a biotechnology company focused
on carbohydrate-based drug development, today announced that it
will announce preliminary clinical data from its Phase I dose
escalation trial the morning of September 8, 2005 and present at
the Roth Capital Partners New York Conference later that morning.
GlycoGenesys, Inc. CEO Bradley J. Carver, is scheduled to give the
presentation. Presentation and Web Casting Information Roth Capital
Partners New York Conference. The Westin New York at Time Square.
Broadway II suite, 3rd Floor at 11:00 a.m. E.D.T. Presentation will
be web cast live and will be available for replay. Please use the
following link to access the web cast or its replay:
http://www.wsw.com/webcast/roth6/glgs/ GlycoGenesys, Inc.
GlycoGenesys, Inc. is a biotechnology company that develops and
licenses compounds based on glycobiology. The Company's drug
candidate GCS-100, a unique compound to treat cancer, has been
evaluated in previous clinical trials at low dose levels in
patients with colorectal, pancreatic and other solid tumors with
stable disease and partial response documented. The Company
currently is conducting a Phase I dose escalation trial to evaluate
higher dose levels of GCS-100LE, a low ethanol formulation of GCS-
100, at Sharp Memorial Hospital, Clinical Oncology Research in San
Diego, California and the Arizona Cancer Center in both Tucson and
Scottsdale, Arizona. In addition, GCS-100LE is being evaluated in a
Phase I/II trial for multiple myeloma. Further clinical trials are
planned for 2005, 2006 and 2007. Further information is available
on GlycoGenesys' web site: www.glycogenesys.com. Safe Harbor
Statement Any statements contained in this release that relate to
future plans, events or performance are forward-looking statements
that involve risks and uncertainties, including, but not limited
to, risks of product development (such as failure to demonstrate
efficacy or safety), risk related to FDA and other regulatory
procedures, market acceptance risks, the impact of competitive
products and pricing, the results of current and future licensing,
joint ventures and other collaborative relationships, risks
relating to raising sufficient capital to fund the Company's
operations, developments regarding intellectual property rights and
litigation, and other risks identified in the Company's Securities
and Exchange Commission filings. Actual results, events or
performance may differ materially. Readers are cautioned not to
place undue reliance on these forward-looking statements, which
speak only as the date hereof. The Company undertakes no obligation
to publicly release the results of any revisions to these forward-
looking statements that may be made to reflect events or
circumstances after the date hereof or to reflect the occurrence of
unanticipated events.
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