Cypress Bioscience, Inc. Announces Second Quarter 2008 Results
SOURCE:
Cypress Bioscience
2008-08-08 05:30:00
Cypress Bioscience, Inc. Announces Second Quarter 2008 Results
SAN DIEGO, CA–(EMWNews – August 8, 2008) – Cypress Bioscience, Inc. (
announced its financial results for the second quarter of 2008. For the
quarter ended June 30, 2008, the Company reported a net loss of
approximately $4.0 million or $0.11 per share basic and diluted compared to
net income of approximately $2.3 million or $0.07 per share basic and
diluted for the corresponding period in 2007. At June 30, 2008, the
Company had cash, cash equivalents and investments totaling $153.4 million.
The Company reported revenues of $1.0 million and $15.2 million for the
quarter and six months ended June 30, 2008, respectively, compared to $5.9
million and $6.9 million for the quarter and six months ended June 30,
2007, respectively. The decrease in revenues during the second quarter of
2008 is primarily due to a $5.0 million milestone payment received from
Forest Laboratories in June 2007 as a consequence of the results of our
second Phase III trial for milnacipran. The increase in revenues during
the six months ended June 30, 2008 is due to a $10.0 million milestone
payment received from Forest Laboratories in February 2008 upon NDA
acceptance and a $3.2 million payment received from Forest Laboratories
also upon NDA acceptance in February 2008 as reimbursement for one-third of
the costs paid in connection with the second Phase III trial for
milnacipran. This increase in revenues during 2008 was partially offset by
the receipt of a $5.0 million milestone payment during 2007. The revenues
recognized during 2008 and 2007 consist solely of amounts earned pursuant
to the Company’s collaboration agreement with Forest Laboratories for the
development and marketing of milnacipran, which was entered into during
January 2004. Such revenues include the recognition of the upfront payment
of $25.0 million over a period of eight years, an additional $1.0 million
license payment received from Forest Laboratories in July 2007 to extend
the territory to include Canada recognized over the remainder of the eight
year amortization period, sponsored development reimbursements, funding
received from Forest Laboratories for certain of our employees devoted to
the development of milnacipran, a $10.0 million milestone payment and $3.2
million payment for reimbursement of certain costs that were received from
Forest Laboratories during the first quarter of 2008 and a $5.0 million
milestone payment received from Forest Laboratories during the second
quarter of 2007.
Total operating expenses for the quarter and six months ended June 30, 2008
were $6.2 million and $25.0 million, respectively, compared to $5.2 million
and $8.6 million for the quarter and six months ended June 30, 2007,
respectively. The increase in operating expenses for the quarter ended
June 30, 2008 was primarily due to costs incurred during the second quarter
in connection with our proof of concept studies for new compounds,
development costs incurred during the second quarter of 2008 in connection
with validation activities for our personalized medicine laboratory
services, which were acquired in connection with the Proprius acquisition
in March 2008, one-time costs owed to Forest Laboratories as agreed upon in
the amendment to our agreement with Forest Laboratories, higher legal fees
incurred during the second quarter of 2008 due to increased patent filing
activity and increased share-based compensation expense related to options
granted in 2008. The increase in operating expenses for the six months
ended June 30, 2008 was primarily due to a charge in the amount of $12.6
million for in-process research and development in connection with the
acquisition of Proprius in March 2008. Also contributing to the increase
in operating expenses in for the six months ended June 30, 2008 was a $1.0
million milestone payment and $0.5 million sublicense fee owed to Pierre
Fabre upon NDA acceptance in connection with our collaboration agreement
with Forest Laboratories, as well as the reasons contributing to the
increase in operating expenses for the three months ended June 30, 2008 as
described above.
About Cypress Bioscience, Inc.
Cypress Bioscience is committed to developing and commercializing
pharmaceutical products and personalized medicine laboratory services that
allow physicians to serve unmet medical needs. Cypress’ strategy involves
evaluating various other potential strategic transactions, including the
potential acquisition of products, product candidates, technologies and
companies, and other alternatives.
For more information about Cypress, please visit the Company’s web site at
This press release, as well as Cypress’ SEC filings and web site at
http://www.cypressbio.com, contain forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995 including
statements about the potential of milnacipran to treat Fibromyalgia and any
new potential strategic transaction. Actual results could vary materially
from those described as a result of a number of factors, including those
set forth in Cypress Annual Report on Form 10-K, the most recent Form 10-Q
and any subsequent SEC filings. In addition, there is the risk that the New
Drug Application that we filed for milnacipran may not be ultimately
approved by the FDA; that we and Forest may elect not to continue
development of milnacipran for any reason; that the results from our third
Phase III clinical trial may not achieve statistical significance, that we
may not be able to protect our milnacipran related patents and proprietary
technology; and that we may not be successful in any of our proof of
concept trials or in developing any of the products or services acquired in
connection with our acquisition of Proprius. Cypress undertakes no
obligation to revise or update these forward-looking statements to reflect
events or circumstances after the date of this press release, except as
required by law.
CYPRESS BIOSCIENCE, INC. Condensed Consolidated Financial Data (In thousands except per share data) Statement of Operations Data: Quarter ended Six months ended June 30, June 30, 2008 2007 2008 2007 -------- --------- -------- --------- (unaudited) (unaudited) Revenues under collaborative agreement $ 1,015 $ 5,949 $ 15,231 $ 6,910 Operating expenses: Research and development 3,009 2,192 5,679 3,186 General and administrative 3,166 2,969 6,704 5,440 In-process research and development - - 12,590 - -------- --------- -------- --------- Total operating expenses 6,175 5,161 24,973 8,626 -------- --------- -------- --------- Interest income 1,169 1,551 2,870 2,834 -------- --------- -------- --------- Net income (loss) $ (3,991) $ 2,339 $ (6,872) $ 1,118 ======== ========= ======== ========= Net income (loss) per share - basic $ (0.11) $ 0.07 $ (0.18) $ 0.03 ======== ========= ======== ========= Shares used in computing net income (loss) per share - basic 37,642 33,716 37,583 32,993 ======== ========= ======== ========= Net income (loss) per share - diluted $ (0.11) $ 0.07 $ (0.18) $ 0.03 ======== ========= ======== ========= Shares used in computing net income (loss) per share - diluted 37,642 35,135 37,583 34,273 ======== ========= ======== ========= Balance Sheet Data: June 30, December 31, 2008 2007 ------------ ------------ (unaudited) Assets Cash, cash equivalents and short-term investments $ 153,428 $ 181,807 Other current assets 547 794 Goodwill 26,466 - Other non-current assets 325 99 ------------ ------------ Total assets $ 180,766 $ 182,700 ============ ============ Liabilities and Stockholders' Equity Current liabilities $ 5,346 $ 4,625 Long-term liabilities 8,391 10,060 Stockholders' equity 167,029 168,015 ------------ ------------ Total liabilities and stockholders' equity $ 180,766 $ 182,700 ============ ============
CONTACT: Michael Hufford, VP Corporate Development Mary Gieson, Investor Relations Cypress Bioscience, Inc. (858) 452-2323 |
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