GlycoGenesys, Inc.'s GCS-100 Subject of Talk By Dr. Finbarr Cotter At The 9th International Conference On Malignant Lymphoma in
2005年6月7日 - 11:31PM
ビジネスワイヤ(英語)
GlycoGenesys, Inc. (Nasdaq: GLGS), a biotechnology company focused
on carbohydrate-based drug development, today announced that Dr.
Finbarr Cotter, Professor, Barts and The London Queen Mary's School
of Medicine UK, is scheduled to give a talk at the 9th
International Conference on Malignant Lymphoma. The talk, entitled
"GCS-100 A Novel Galectin-3 Antagonist and Caspace-9 Activating
Therapy For Indolent B-Cell Malignancies", will be given during
Session 16, New Immunological Principles (Room C) at 8:30 a.m. CEST
June 11, 2005. Management's Comments Bradley J Carver, the
Company's CEO and President stated, "We look forward to Dr.
Cotter's new research on GCS-100 being presented to this
distinguished global audience of clinicians, cancer researchers,
and members of the biotechnology and pharmaceutical industry."
GlycoGenesys, Inc. GlycoGenesys, Inc. is a biotechnology company
focused on carbohydrate-based drug development. The Company
currently is conducting a Phase I dose escalation trial of
GCS-100LE, a unique compound to treat cancer, in patients with
solid tumors at Sharp Memorial Hospital, Clinical Oncology Research
in San Diego, California and the Arizona Cancer Center at Tucson
and at Scottsdale, Arizona. In addition, the Company is conducting
a Phase I/II dose escalation trial of GCS-100LE in multiple myeloma
at the Dana-Farber Cancer Institute in Boston, Massachusetts.
Further clinical trials are planned for 2005. The Company's
headquarters are located in Boston, Massachusetts with a laboratory
in Cambridge, Massachusetts. Additional 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, the results
of financing efforts, 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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