WARRINGTON, Pa., Feb. 23, 2006 (PRIMEZONE) -- Discovery Laboratories, Inc. (Nasdaq:DSCO) today announced financial results for the fourth quarter and year ended December 31, 2005. The Company will host a conference call Friday, February 24th at 10:00 AM EST. The call in number is 866-332-5218.
For the quarter ended December 31, 2005, the Company reported a net loss of $29.4 million, or $0.51 per share, on 57.8 million weighted average common shares outstanding, compared to a net loss of $20.1 million, or $0.42 per share, on 47.2 million weighted average shares outstanding for the same period in 2004. For the twelve months ended December 31, 2005, the Company reported a net loss of $58.9 million, or $1.09 per share, on 54.1 million weighted average shares outstanding, compared to a net loss of $46.2 million, or $1.00 per share, on 46.2 million weighted average shares outstanding for the same period in 2004. As of December 31, 2005, the Company had 61.0 million shares outstanding.
In December 2005, the Company purchased the manufacturing operations of Laureate Pharma, Inc. (Laureate) in Totowa, NJ for $16.0 million and incurred additional related expenses of $0.8 million. Included in the fourth quarter 2005 net loss is a charge, classified as in-process research and development, of $16.8 million or $0.29 per share related to the manufacturing purchase. Included in the fourth quarter 2004 net loss is a charge, classified as corporate partnership restructuring, of $8.1 million, or $0.17 per share, associated with the restructuring of strategic collaborations with Quintiles Transnational Corp. (Quintiles) and Laboratorios del Dr. Esteve S.A. (Esteve).
Excluding these charges, the net loss for the fourth quarter 2005 was $12.6 million, or $0.22 per share, compared to a net loss of $11.9 million, or $0.25 per share for the same period in 2004 and, for the twelve months ended December 31, 2005, the net loss was $42.1 million, or $0.78 per share, compared to a net loss of $38.1 million, or $0.82 per share, for the same period in 2004.
As of December 31, 2005, the Company had cash and marketable securities of $50.9 million, a net increase of $0.6 million from the previous quarter. Aggregate cash outflows for the fourth quarter were $28.6 million, which consisted of $12.6 million used in operating and investing activities and $16.0 million for the purchase of the manufacturing operations of Laureate. These cash outflows were offset by aggregate cash inflows of $29.2 million, which consisted of (i) a registered direct public offering resulting in net proceeds of $18.9 million; (ii) a registered direct public offering to Esteve, resulting in net proceeds of $4.5 million; (iii) a financing pursuant to the Company's Committed Equity Financing Facility (CEFF) resulting in net proceeds of $3.2 million; and (iv) $2.6 million, of which $2.4 million was associated with financing the manufacturing purchase, from the use of the capital lease financing arrangement with General Electric Capital Corporation (GECC).
As of December 31, 2005, the Company had $47.6 million available under the CEFF, subject to certain conditions. Additionally, under the Company's $9.0 million capital lease financing arrangement with GECC, $4.9 million is outstanding ($1.6 million classified as current liabilities and $3.3 million as long-term liabilities) and $2.6 million remains available for use. The Company's $8.5 million credit facility with Quintiles is fully outstanding, due in December 2006 and now classified as a current liability.
Robert J. Capetola, Ph.D., President and Chief Executive Officer of Discovery, commented, "This past quarter, we believe we have significantly strengthened our Company, both financially and operationally in preparation for the potential FDA approval in April 2006 and U.S. commercial launch in the second quarter of 2006 of our lead product, Surfaxin(R). We have raised $29.0 million in capital, secured our own manufacturing operation -- a key strategic asset for Surfaxin and our pipeline, and are now in the final stage of building our specialty neonatal U.S. commercial capability. Important to the development of our surfactant replacement therapy (SRT) pipeline, we established a strategic alliance with Chrysalis Technologies (a division of Philip Morris USA) where we acquired rights to a novel aerosol generating technology being developed to enable the delivery of SRT to the deep lung. The successful application of our SRT and Chrysalis' aerosol technology holds the promise, for the first time, of producing surfactant-based therapies that may revolutionize the treatment of serious respiratory conditions such as neonatal respiratory failure, acute lung injury, chronic obstructive pulmonary disorder, asthma, cystic fibrosis and others."
Review of Operating Results - Three and Twelve Months Ended December 31, 2005
The Company reported a net loss of $29.4 million and $58.9 million for the three and twelve months ended December 31, 2005, respectively. Excluding the $16.8 million charge in the fourth quarter of 2005 for the purchase of the manufacturing operation and the $8.1 million charge in the fourth quarter of 2004 for the restructuring of strategic collaborations, the net loss increased by $0.7 million and $4.0 million for the three and twelve months ended December 31, 2005, respectively, as compared to the same periods in 2004. The change in the net loss is primarily due to:
i) manufacturing activities (included in research and development
expenses) to support the production of clinical and commercial
drug supply for the Company's SRT programs, including Surfaxin,
in conformance with current Good Manufacturing Practices (cGMPs).
For the three and twelve months ended December 31, 2005, costs
associated with these manufacturing activities were $4.4 million
and $11.4 million, respectively, an increase of $2.0 million and
$4.4 million compared to the same periods in 2004. Expenditures
in 2005 for manufacturing activities include, but are not limited
to, the implementation of enhancements to quality controls,
process assurances and documentation requirements that support
the production process predominantly at Laureate's Totowa, NJ
operation (the Company's contract manufacturer at that time) in
response to the FDA 483 inspectional observations. Additionally,
the increase in expenses in the fourth quarter of 2005 were due
to enhancements to Laureate's Totowa, NJ operations and facility
for the production of Surfaxin, SRT formulations and aerosol
development capabilities. In December 2005, the Company purchased
the manufacturing operation of Laureate in Totowa, NJ;
ii) research and development activities related to the advancement
of the Company's SRT pipeline. For the three and twelve months
ended December 31, 2005, costs associated with these activities,
excluding manufacturing activities, were $3.1 million and $12.7
million, respectively, a decrease of $1.6 million and $6.1
million compared to the same periods in 2004. The decrease is
primarily due to costs in 2004 associated with clinical and
regulatory activities for Surfaxin for RDS, principally the NDA
filing, a related milestone payment for the license of Surfaxin,
and follow-up clinical activity pertaining to the two Phase 3
clinical trials. For the three and twelve months ended December
31, 2005, research and development activities primarily reflect
regulatory activities associated with Surfaxin for RDS
(specifically the U.S. FDA Approvable Letter and the EMEA
Marketing Authorization Application) and clinical activities
related to the Phase 2 clinical trials for Acute Respiratory
Distress Syndrome (ARDS) in adults, Bronchopulmonary Dysplasia
(BPD, also known as Chronic Lung Disease) in premature infants,
and Aerosurf for Neonatal Respiratory Failure;
iii) pre-launch commercialization activities (included in general
and administrative expenses) related to the Company building its
own specialty pulmonary United States commercial organization to
focus initially on the commercial and medical promise of its SRT
to address respiratory therapies for the Neonatal Intensive Care
Unit (NICU). Expenditures are for sales, marketing and medical
affairs activities in anticipation of the potential approval and
launch of Surfaxin for Respiratory Distress Syndrome (RDS) in
the second quarter of 2006. For the three and twelve months
ended December 31, 2005, costs associated with pre-launch
commercialization activities were $2.9 million and $10.1 million,
respectively, an increase of $0.3 million and $4.2 million
compared to the same prior year periods;
iv) general and administrative activities in preparation for
managing a fully-integrated commercial biotechnology
organization. For the three and twelve months ended December 31,
2005, costs associated with these activities, excluding
pre-launch commercialization activities, were $2.4 million and
$8.4 million respectively, with no change compared to the three
months ended December 31, 2004 and an increase of $1.0 million
compared to the twelve months ended December 31, 2004. These
expenditures include building management and systems for
financial and information technology capabilities, business
development activities related to potential strategic
collaborations, legal activities related to the preparation and
filing of patents in connection with the expansion of our SRT
pipeline, facilities expansion activities to accommodate existing
and future growth, and corporate governance initiatives to comply
with the Sarbanes-Oxley Act; and
v) the restructuring, in December 2004, of our strategic alliance
with Esteve to develop, market and sell Surfaxin in Southern
Europe. Revenues from this alliance decreased by $0.1 million and
$1.1 million for the three and twelve months ended December 31,
2005, respectively, compared to the same prior year periods.
Selective Updates on Discovery's Business in Q4 2005
-- In October, the U.S. Food and Drug Administration (FDA)
accepted the Company's response to the Approvable Letter for
Surfaxin for the prevention of RDS in premature infants. The FDA
has established April 2006 as its target to complete its review
of the Surfaxin NDA.
-- In December, the Company entered into a strategic alliance with
Chrysalis Technologies, a division of Philip Morris USA Inc., for
the Company to develop and commercialize aerosolized surfactant
replacement therapies (aSRT) to address a broad range of serious
respiratory conditions. This alliance focuses on therapies for
hospitalized patients, including those in the NICU, pediatric
intensive care unit and the adult intensive care unit, and can be
expanded into other hospital applications and ambulatory
settings. The Company and Chrysalis will utilize their respective
capabilities and resources to support and fund the design and
development of integrated drug-device systems that can be
uniquely customized to address specific respiratory diseases and
patient populations. Chrysalis is responsible for developing the
design for the aerosol device platform, patient interface and
disposable dose packets. The Company is responsible for aSRT drug
formulations, clinical and regulatory activities, and the
manufacturing and commercialization of the drug-device products.
The Company has exclusive rights to Chrysalis' aerosolization
technology for use with pulmonary surfactants for all respiratory
diseases and conditions in hospital and ambulatory settings.
Chrysalis receives from the Company a tiered royalty, the base
royalty applies to aggregate net sales of less than $500 million,
increases on aggregate net sales in excess of $500 million, and
increases again on aggregate net sales of alliance products in
excess of $1 billion.
-- In December, the Company acquired the manufacturing operation
of Laureate in Totowa, NJ for $16.0 million. The acquisition is
intended to provide the Company with operational control and
improved economics for the potential commercial and clinical
production of Surfaxin and its SRT products. The Company's
manufacturing operation is located in approximately 21,000 square
feet of leased pharmaceutical manufacturing and development space
that is specifically designed for the production of sterile
pharmaceuticals in compliance with cGMP requirements.
About Discovery Labs
Discovery Laboratories, Inc. is a biotechnology company developing its proprietary surfactant technology as Surfactant Replacement Therapies (SRT) for respiratory diseases. Surfactants are produced naturally in the lungs and are essential for breathing. Discovery Labs' technology produces a precision-engineered surfactant that is designed to closely mimic the essential properties of natural human lung surfactant. Discovery Labs believes that through its technology, pulmonary surfactants have the potential, for the first time, to address respiratory diseases where there are few or no approved therapies available.
Discovery Labs' SRT pipeline is initially focused on the most significant respiratory conditions prevalent in the neonatal intensive care unit. The Company's lead product, Surfaxin(R), for the prevention of Respiratory Distress Syndrome (RDS) in premature infants, has received an Approvable Letter from the FDA and is under review for approval in Europe by the EMEA. Surfaxin is also being developed for the prevention and treatment of Bronchopulmonary Dysplasia (BPD, also known as Chronic Lung Disease) in premature infants. Discovery Labs is preparing to conduct multiple Phase 2 pilot studies with Aerosurf, aerosolized SRT administered through nasal continuous positive airway pressure (nCPAP), for the treatment of neonatal respiratory failure.
To address the various respiratory conditions affecting pediatric, young adult and adult patients in the critical care and other hospital settings, Discovery Labs is conducting a Phase 2 clinical trial to address Acute Respiratory Distress Syndrome (ARDS) in adults, and is also developing aerosol formulations of SRT to address Acute Lung Injury (ALI), asthma, COPD, and other respiratory conditions.
For more information, please visit our corporate website at www.Discoverylabs.com.
To the extent that statements in this press release are not strictly historical, including statements as to business strategy, outlook, objectives, future milestones, plans, intentions, goals, future financial conditions, future collaboration agreements, the success of Discovery's product development, events conditioned on stockholder or other approval, or otherwise as to future events, all such statements are forward-looking, and are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. These forward-looking statements are subject to certain risks and uncertainties that could cause actual results to differ materially from the statements made. Among the factors which could affect Discovery's actual results and could cause results to differ from those contained in these forward-looking statements are the risk that financial conditions may change, risks relating to the progress of Discovery's research and development, the risk that Discovery will not be able to raise additional capital or enter into additional collaboration agreements (including strategic alliances for aerosol and Surfactant Replacement Therapies), risk that Discovery will not be able to develop a successful sales and marketing organization in a timely manner, if at all, risk that Discovery's internal sales and marketing organization will not succeed in developing market awareness of Discovery's products, risk that Discovery's internal sales and marketing organization will not be able to attract or maintain qualified personnel, risk of delay in the FDA's or other health regulatory authorities' approval of any applications filed by Discovery, risks that any such regulatory authority will not approve the marketing and sale of a drug product even after acceptance of an application filed by Discovery for any such drug product, risks relating to the ability of Discovery's third party contract manufacturers and development partners to provide Discovery with adequate supplies of drug substance, drug products and expertise for completion of any of Discovery's clinical studies, risks relating to drug manufacturing by Discovery, risks relating to the integration of manufacturing operations into Discovery's existing operations, other risks relating to the lack of adequate supplies of drug substance and drug product for completion of any of Discovery's clinical studies, risks relating to the ability of the Company and its collaborators to develop and successfully commercialize products that will combine our drug products with innovative aerosolization technologies, risks relating to the significant, time-consuming and costly research, development, pre-clinical studies, clinical testing and regulatory approval for any products that we may develop independently or in connection with our collaboration arrangements, and risks relating to the development of competing therapies and/or technologies by other companies. Companies in the pharmaceutical and biotechnology industries have suffered significant setbacks in advanced clinical trials, even after obtaining promising earlier trial results. Data obtained from tests are susceptible to varying interpretations, which may delay, limit or prevent regulatory approval. Those associated risks and others are further described in Discovery's filings with the Securities and Exchange Commission including the most recent reports on Forms 10-K, 10-Q and 8-K, and any amendments thereto.
Condensed Consolidated Statement of Operations
(in thousands, except per share data)
Three Months Ended Year Ended
December 31, December 31,
(unaudited)
------------------- -------------------
2005 2004 2005 2004
-------- -------- -------- --------
Revenues from collaborative
agreements $ 29 $ 134 $ 134 $ 1,209
Operating expenses:
Research and development 7,477 7,037 24,137 25,793
General and administrative 5,323 4,958 18,505 13,322
In-process research &
development 16,787 -- 16,787 --
Corporate partnership
restructuring -- 8,126 -- 8,126
-------- -------- -------- --------
Total expenses 29,587 20,121 59,429 47,241
Operating loss (29,558) (19,987) (59,295) (46,032)
Other income / (expense) 202 (65) 391 (171)
-------- -------- -------- --------
Net loss $(29,356) $(20,052) $(58,904) $(46,203)
======== ======== ======== ========
Net loss per common share $ (0.51) $ (0.42) $ (1.09) $ (1.00)
Weighted average number of
common shares outstanding 57,843 47,236 54,094 46,179
Condensed Consolidated Balance Sheets
(in thousands)
December 31,
2005 2004
------- -------
ASSETS
Current Assets:
Cash and marketable securities $50,908 $32,654
Prepaid expenses and other current assets 560 688
------- -------
Total Current Assets 51,468 33,342
Property and equipment, net 4,322 4,063
Other assets 218 232
------- -------
Total Assets $56,008 $37,637
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LIABILITIES AND STOCKHOLDERS' EQUITY
Current Liabilities:
Accounts payable and accrued expenses $ 7,540 $ 7,969
Credit facility 8,500 --
Capitalized leases and other
liabilities, current portion 1,568 854
------- -------
Total Current Liabilities 17,608 8,823
Long-Term Liabilities:
Credit facility -- 5,929
Capitalized leases and other liabilities,
long-term portion 3,562 1,788
------- -------
Total Liabilities 21,170 16,540
Stockholders' Equity 34,838 21,097
------- -------
Total Liabilities and
Stockholders' Equity $56,008 $37,637
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