GlycoGenesys, Inc. (NASDAQ:GLGS), a biotechnology company focused
on carbohydrate drug development, today announced results from its
recently filed Form 10-Q for the quarter-ended June 30, 2005.
Select Financial Highlights: The net loss applicable to common
stock for the three months ended June 30, 2005 and 2004 was
$(2,292,454), or $(0.22) per share, and $(2,723,822), or $(0.32)
per share, respectively. For the six months ended June 30, 2005 and
2004 the net loss applicable to common stock was $(4,921,841), or
$(0.48) per share, and $(5,488,547), or $(0.66) per share,
respectively. The net loss applicable to common stock for the three
months ended June 30, 2005 and 2004 included a $208,940 and
$113,771 charge for the accretion or accrual of preferred stock
dividends, respectively. The net loss applicable to common stock
for the six months ended June 30, 2005 and 2004 included a $329,359
and $227,542 charge for the accretion or accrual of preferred stock
dividends, respectively. "The Company's net loss applicable to
common stock was approximately $430,000 less during the second
quarter compared to the same period last year mainly due to reduced
drug production and development expenses, as well as legal costs
offset in part by costs associated with the special stockholders
meeting held in May and higher preferred stock dividends," stated
John W. Burns, SVP and CFO of GlycoGenesys, Inc. "For the first
half of the year, the net loss applicable to common stock was
approximately $570,000 less than the same period last year mainly
due to lower drug production and development expenses, as well as
legal costs offset by higher clinical trial costs, preferred
dividends and the costs associated with the special stockholders
meeting in May," added Mr. Burns. "In May, we closed on an
additional $4.5 million in gross proceeds in a private placement to
institutions and other accredited investors following shareholder
approval of the transaction. This allows us to continue with our
current Phase I dose escalation trial in solid tumors and Phase
I/II trial in multiple myeloma, as well as with the preparations
for initiating the planned trial for chronic lymphocytic leukemia,"
stated Mr. Burns. "Moreover, we continue to actively pursue a
long-term funding relationship with either a biotechnology or
pharmaceutical company, or with fundamental, long-term investors
because we believe it would further validate our technology and
provide the capital to further fund and expand our clinical trial
program and pipeline development," added Mr. Burns. Select
Operational Achievements For The Quarter: During the second
quarter, the Company accomplished many operational achievements,
including: -- The presentation by Dr. Finbarr Cotter of Barts
Medical School in London of data showing that GCS-100 causes cell
death in chronic lymphocytic leukemia and lymphoma cells by
blocking Galectin-3's ability to co-locate with Bcl-2; -- The
issuance of U.S. Patent No. 6,890,906 which covers the use of
GCS-100 and other modified pectins to control angiogenesis and to
treat diseases in which angiogenesis plays a role; and -- The
initiation of a second site, the Lucy Curci Cancer Center in Rancho
Mirage, California, in the Company's Phase I/II multiple myeloma
trial. A copy of the 2005 Form 10-Q and other SEC filings are
available on the Company website, www.glycogenesys.com and is also
available on the SEC's website, www.sec.gov. -0- *T CONFERENCE CALL
ALERT GlycoGenesys, Inc. Reports Financial Results and Events of
Quarter-Ended June 30, 2005 Date: August 22, 2005 Time: 11:00 a.m.
E.D.S.T. Please call: 1-877-451-8949 OR 1-706-679-0877
(international callers) to be connected between 10:50 p.m. and
11:00 a.m. E.D.S.T. Call Leaders: Bradley J Carver, President and
CEO, and John W. Burns, SVP and CFO The call will be archived on
the Company's website. GlycoGenesys, Inc. CONDENSED CONSOLIDATED
STATEMENTS OF OPERATIONS (Unaudited) Three Months Ended Six Months
Ended June 30, June 30, 2005 2004 2005 2004 Operating expenses:
Research and development $ 873,646 $ 1,217,217 $ 2,393,750 $
2,596,692 General and administrative 1,222,757 1,453,592 2,218,186
2,735,443 Total operating expenses 2,096,403 2,670,809 4,611,936
5,332,135 Operating loss (2,096,403) (2,670,809) (4,611,936)
(5,332,135) Interest income 12,790 6,234 18,205 13,710 Other income
99 54,524 1,249 57,420 Total other income 12,889 60,758 19,454
71,130 Net loss (2,083,514) (2,610,051) (4,592,482) (5,261,005)
Preferred stock dividends accreted or accrued (208,940) (113,771)
(329,359) (227,542) Net loss applicable to common stock $
(2,292,454)$(2,723,822)$(4,921,841)$(5,488,547) Basic and diluted
net loss per common stock $ (0.22)$ (0.32)$ (0.48)$ (0.66) Weighted
average number of common shares outstanding 10,626,841 8,445,207
10,355,612 8,359,001 CONDENSED CONSOLIDATED BALANCE SHEETS June 30,
2005 December 31, 2004 (Unaudited) Cash and cash equivalents $
4,139,577 $ 2,245,790 Working capital 2,228,148 828,605 Total
assets 5,006,218 3,105,176 Total stockholders' equity $ 2,707,754 $
1,346,010 *T About 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 at the Dana-Farber Cancer Institute in Boston,
Massachusetts and the Lucy Curci Cancer Center in Rancho Mirage,
California. 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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