Targanta Therapeutics Corp (MM) (NASDAQ:TARG)
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Targanta Therapeutics Corporation (Nasdaq: TARG) today reported
financial results for the second quarter and six months ended June 30,
2008.
Targanta reported a net loss of $17.1 million for the three months ended
June 30, 2008, compared to a net loss of $12.1 million for the same
period in 2007. This increase is primarily due to increases in research
and development (R&D) expense including pre-clinical, clinical and
manufacturing expenses in preparation for the potential commercial
launch of the Company’s lead antibiotic
candidate, oritavancin. The increase in R&D expense also includes
regulatory filing fees associated with the submission of Targanta’s
Marketing Authorization Application (MAA), which seeks approval to
commercialize oritavancin in the European Union. The net loss is also
attributable to an increase in general and administrative expenses,
primarily as a result of developing the infrastructure to support the
potential commercial launch of oritavancin.
For the six months ended June 30, 2008, the Company reported a net loss
of $34.7 million compared to a net loss of $30.8 million for the same
period in 2007.
The calculation of net loss for the second quarter and six months ended
June 30, 2008 includes stock-based compensation expense of $0.9 million
and $1.3 million, respectively.
The Company had cash, cash equivalents and short-term investments
totaling $58.7 million as of June 30, 2008 and approximately 21.0
million shares outstanding.
About Targanta Therapeutics
Targanta Therapeutics Corporation (Nasdaq: TARG) is a biopharmaceutical
company focused on developing and commercializing innovative antibiotics
to treat serious infections in the hospital and other institutional
settings. The Company’s pipeline includes an
intravenous version of oritavancin, a semi-synthetic lipoglycopeptide
antibiotic currently awaiting U.S. and EU regulatory approval; a program
to develop an oral version of oritavancin; and, a number of
antibacterial agents in pre-clinical development. The Company has
operations in Cambridge, MA, Indianapolis, IN, and Montreal, Québec,
Canada. For more information on Targanta, visit www.targanta.com.
Safe Harbor Statement
This press release contains “forward-looking
statements” that are made pursuant to the safe
harbor provisions of the Private Securities Litigation Reform Act of
1995. These are statements that are predictive in nature, that depend
upon or refer to future events or conditions or that include words such
as “potential,” “may,”
"will," "expects," "projects," "anticipates," "estimates," "believes,"
"intends," "plans," "should," "seeks," “hope”
and similar expressions. Such statements include, but are not limited
to, the potential commercial launch of oritavancin and approval to
commercialize oritavancin in the European Union. Forward-looking
statements involve known and unknown risks and uncertainties that may
cause actual future results to differ materially from those projected or
contemplated in the forward-looking statements. Forward-looking
statements may be significantly impacted by certain risks and
uncertainties described in Targanta’s filings
with the Securities and Exchange Commission. The risks and uncertainties
referred to above include, but are not limited to, delays in obtaining
or a failure to obtain regulatory approval for Targanta’s
product candidates; unfavorable clinical trial results; Targanta’s
potential inability to initiate and complete pre-clinical studies and
clinical trials for its product candidates; the possibility that results
of pre-clinical studies are not necessarily predictive of clinical trial
results; and those other risk factors that are described more fully in
the Company’s filings with the Securities and
Exchange Commission. Targanta does not undertake any obligation to
update any of these forward-looking statements to reflect a change in
its views or events or circumstances that occur after the date of this
release.
CONSOLIDATED STATEMENTS OF OPERATIONS
(in thousands, except share and per share amounts)
(unaudited)
Three Months Ended
June 30,
Six Months Ended
June 30,
2008
2007
2008
2007
Operating expenses
Research and development (1)
$
12,859
$
9,405
$
27,138
$
14,844
Acquired in-process research and development
—
—
—
9,500
General and administrative (1)
4,189
2,847
7,807
4,782
Total operating expenses
17,048
12,252
34,945
29,126
Other income (expense)
Interest income
466
556
1,334
1,014
Interest expense
(602
)
273
(1,245
)
(1,937
)
Foreign exchange gain (loss)
5
(789
)
(14
)
(853
)
Other income (expense), net
(131
)
40
75
(1,776
)
Loss before income tax benefit
(17,179
)
(12,212
)
(34,870
)
(30,902
)
Income tax benefit
74
83
140
54
Net loss
$
(17,105
)
$
(12,129
)
$
(34,730
)
$
(30,848
)
Net loss per share—basic and diluted
$
(0.82
)
$
(479.78
)
$
(1.66
)
$
(1,229.07
)
Weighted average number of common shares used in net loss per share—basic
and diluted
20,970,490
25,282
20,969,873
25,282
(1) Amounts include stock-based
compensation expense, as follows:
Research and development
$
312
$
739
$
569
$
747
General and administrative
$
546
$
592
$
761
$
603
CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands)
(unaudited)
June 30,
2008
December 31, 2007
Assets
Current assets:
Cash, cash equivalents and short-term investments
$
58,682
$
89,753
Restricted cash
491
506
Investment tax credits recoverable
516
757
Prepaid expenses and other current assets
1,372
1,630
Total current assets
61,061
92,646
Property and equipment, net
1,276
1,350
Deferred financing costs
86
103
Deposits
72
50
Total assets
$
62,495
$
94,149
Liabilities and Stockholders’ Equity
Current liabilities:
Accounts payable and accrued expenses
$
12,578
$
6,591
Income tax payable
674
2,731
Current portion of deferred rent
34
24
Current portion of long-term debt
6,591
5,480
Total current liabilities
19,877
14,826
Other long-term liabilities
259
163
Long-term debt
10,991
14,287
Stockholders’ equity
31,368
64,873
Total liabilities and stockholders’ equity
$
62,495
$
94,149