Adolor Corporation Reports First Quarter 2008 Financial Results
April 28 2008 - 9:00AM
Business Wire
Adolor Corporation (Nasdaq:ADLR) today reported financial results
for the three months ended March 31, 2008. For the three months
ended March 31, 2008, the company reported a net loss of $9.1
million or $(0.20) per basic and diluted share, compared to a net
loss of $13.2 million or $(0.29) per basic and diluted share for
the same period in 2007. Contract revenues for the quarter ended
March 31, 2008 were $6.2 million, compared to $1.8 million in the
same period of 2007. This increase was primarily due to an increase
in amortization of up front fees associated with the Pfizer Inc
collaboration of $3.5 million and an increase in expenses incurred
by us that are reimbursable by Pfizer under our collaboration
agreement of $0.8 million. Research and development expenses in the
first quarter of 2008 were $11.4 million, compared to $11.6 million
for the same period in 2007. Expense decreases in the ENTEREG
program of $0.6 million and in the combination program of $0.6
million were the result of reduced spending as a result of the
alvimopan Investigational New Drug applications being on clinical
hold. In addition, the Delta program expenses decreased by $0.5
million due to reduced manufacturing costs as compared to the
quarter ended March 31, 2007. These decreases were offset by an
increase of $1.8 million in our other preclinical programs.
Marketing, general and administrative expenses decreased to $5.5
million in the first quarter of 2008 from $5.8 million in the first
quarter of 2007, as a result of decreased personnel expenses,
including stock-based compensation expenses associated with
Statement of Financial Accounting Standards No.123R. As of March
31, 2008, the Company had $155.2 million in cash, cash equivalents
and short-term investments. About Adolor Corporation Adolor
Corporation (Nasdaq:ADLR) is a biopharmaceutical company
specializing in the discovery, development and commercialization of
novel prescription pain management products. Adolor has two lead
product candidates in development: ENTEREG� (alvimopan) for the
management of the gastrointestinal side effects associated with
opioid use; and, novel Delta opioid receptor agonists for a variety
of pain indications. Adolor and GlaxoSmithKline are collaborating
in the worldwide development and commercialization of ENTEREG in
multiple indications. Adolor and Pfizer are collaborating in the
worldwide development and commercialization of two Delta agonists
for pain. Adolor also has a number of discovery research programs
focused on the identification of novel compounds for the treatment
of pain. By applying its knowledge and expertise in pain
management, along with ingenuity, Adolor is seeking to make a
positive difference for patients, caregivers and the medical
community. For more information, visit www.adolor.com. This
release, and oral statements made with respect to information
contained in this release, may constitute forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995. Such forward-looking statements include those
which express plan, anticipation, intent, contingency, goals,
targets or future development and/or otherwise are not statements
of historical fact. These statements are based upon management's
current expectations and are subject to risks and uncertainties,
known and unknown, which could cause actual results and
developments to differ materially from those expressed or implied
in such statements. Such known risks and uncertainties relate to,
among other factors: the risk that Adolor may not receive
regulatory approval of ENTEREG � (alvimopan) for POI, OBD, or any
other indication; the risk that the PDUFA date extended to May 10,
2008 is further extended or not met; the risk that a risk
management plan acceptable to the FDA could materially adversely
affect the commercial prospects for ENTEREG, if regulatory approval
is achieved; the risk that Adolor may not be able to adequately
address the deficiencies in the November 2006 FDA approvable
letter; the risk that Adolor may not obtain FDA approval for
ENTEREG in POI, whether due to Adolor's inability to provide
additional data satisfactory to the FDA to obtain approval for the
NDA, the adequacy of the safety and efficacy data from all of the
ENTEREG studies, changing regulatory requirements, the risk that
the FDA may not agree with Adolor's and GSK's analyses of the
ENTEREG studies (including Study 014) and may evaluate the results
of these studies by different methods or conclude that the results
from the studies, whether or not statistically significant, do not
support safety, efficacy, a favorable risk/benefit profile, or
there were human errors in the conduct of the studies, or
otherwise; adverse safety findings in any ENTEREG studies; the risk
that the alvimopan Investigational New Drug Applications (INDs)
remain on clinical hold indefinitely; the risk that filing targets
for regulatory submissions or user fee goal dates are not met; the
risk that the results of other clinical trials of Adolor's drug
product candidates, including our Delta product candidates are not
positive; the risk of product liability claims; reliance on third
party manufacturers; the costs, delays and uncertainties inherent
in scientific research, drug development, clinical trials and the
regulatory approval process; Adolor's history of operating losses
since inception and its need for additional funds to operate its
business; Adolor's reliance on its collaborators, including GSK, in
connection with the development and commercialization of ENTEREG;
market acceptance of Adolor's products, if regulatory approval is
achieved; competition; and securities litigation. Further
information about these and other relevant risks and uncertainties
may be found in Adolor's Reports on Form 8-K, 10-Q and 10-K filed
with the U.S. Securities and Exchange Commission. Adolor urges you
to carefully review and consider the disclosures found in its
filings which are available in the SEC EDGAR database at
http://www.sec.gov and from Adolor at http://www.adolor.com. Given
the uncertainties affecting pharmaceutical companies in the
development stage, you are cautioned not to place undue reliance on
any such forward-looking statements, any of which may turn out to
be wrong due to inaccurate assumptions, unknown risks,
uncertainties or other factors. Adolor undertakes no obligation to
(and expressly disclaims any such obligation to) publicly update or
revise the statements made herein or the risk factors that may
relate thereto whether as a result of new information, future
events, or otherwise. This press release is available on the
website http://www.adolor.com. [Financial data table follows]
ADOLOR CORPORATION STATEMENTS OF OPERATIONS DATA (Unaudited) � �
FOR THE THREE MONTHS ENDED MARCH 31, � 2008 2007 � REVENUES
Contract revenues $ 6,211,024 $ 1,821,003 � OPERATING EXPENSES
Research and development 11,421,072 11,573,017 Marketing, general
and administrative � 5,548,530 � 5,817,302 � Total operating
expenses � 16,969,602 � 17,390,319 � Loss from operations
(10,758,578) (15,569,316) Interest income and other, net �
1,703,019 � 2,360,865 Net loss $ (9,055,559) $ (13,208,451) � Basic
and diluted net loss per share $ (0.20) $ (0.29) � Shares used in
computing basic and diluted net loss per share 45,948,066
45,920,368 � � BALANCE SHEET DATA (Unaudited) � MARCH 31, DECEMBER
31, 2008 2007 � Cash, cash equivalents and short-term investments $
155,214,631 $ 167,189,499 Working capital 136,589,480 147,543,363
Total assets 166,414,539 178,676,652 Total stockholders' equity
105,290,534 112,353,478
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