CONCORD, Calif.--(BUSINESS WIRE)--
Cerus Corporation (NASDAQ: CERS) today announced financial results for
the third quarter ended September 30, 2012.
Third quarter 2012 results:
-
Product revenue of $8.3 million, a 6% increase from the $7.8 million
recognized during the third quarter of 2011;
-
No government grant revenue recognized during the third quarter of
2012, compared to $1.5 million recognized during the third quarter of
2011;
-
Operating expenses of $8.2 million compared to $7.2 million incurred
during the third quarter of 2011; and
-
Cash of $26.7 million at September 30, 2012.
2012 year-to-date results:
-
Product revenue of $26.2 million, a 26% increase from the $20.7
million recognized during the first nine months of 2011;
-
Government grant revenue of $0.1 million, compared to $1.9 million
recognized during the first nine months of 2011; and
-
Operating expenses of $24.5 million compared to $22.9 million incurred
during the first nine months of 2011.
”Based on recent positive discussions with the FDA, Cerus now plans to
move forward with a modular Premarket Approval Application for the
INTERCEPT Blood System for plasma in the United States,” said William
‘Obi‘ Greenman, president and chief executive officer of Cerus
Corporation. “With regard to our commercial operations, demand for
INTERCEPT kits continues to be healthy, and we remain confident in our
guidance for 2012 for revenue of $34 million to $36 million.”
INTERCEPT plasma PMA modular submission
Recently, Cerus discussed with the FDA the clinical requirements for
proceeding with a Premarket Approval Application, or PMA, for the
INTERCEPT plasma system. Based upon those discussions, Cerus believes
that existing clinical data is sufficient to begin the PMA submission
process and intends to proceed with a modular PMA, pending FDA approval
of an application shell. The modular PMA process is a compilation of
sections or "modules" submitted at different times that together become
a complete PMA. The modular approach increases the likelihood that an
applicant will be able to resolve deficiencies identified by the FDA
earlier in the review process than would occur with a traditional PMA
application.
Revenue
Product revenue for the third quarter of 2012 was $8.3 million, and
represented a 6% increase from the third quarter of 2011. The increase
in product revenue was driven by the 14% increase in year-over-year
demand for INTERCEPT disposable kits.
No government grant revenue was recognized during the third quarter of
2012, as government grants in support of the Company’s red blood cell
system had been fully utilized by January 2012. This compared to $1.5
million of government grant revenue recognized during the third quarter
of 2011.
Product revenue for the first nine months of 2012 was $26.2 million, and
represented a 26% increase from the first nine months of 2011. The
increase in product revenue during the first nine months of 2012 over
2011 was driven primarily by a 34% increase in demand for INTERCEPT
disposable kits.
Government grant revenue for the first nine months of 2012 was $0.1
million, down from $1.9 million recognized during the first nine months
of 2011. The last government grant awarded to Cerus in support of the
Company’s red blood cell system occurred in August 2011. The Company
does not currently expect any government grant revenue for the
foreseeable future.
Gross Margins
Gross margins on product sales for the third quarter of 2012 were 47%,
compared to 39% reported for the third quarter of 2011. Gross margins on
product sales for the first nine months of 2012 were 41%, compared to
40% for same period in 2011. The improvement in gross margins on product
sales was driven by a more favorable mix of products sold and lower 2012
carrying costs resulting from higher levels of manufacturing.
Operating Expenses
Total operating expenses for the third quarter of 2012 were $8.2
million, compared to $7.2 million for the third quarter of 2011. Total
operating expenses for the first nine months of 2012 were $24.5 million,
compared to $22.9 million for the first nine months of 2011. The
increase in operating expenses in both periods was related to increases
in selling, general and administrative expenses in support of growing
the commercial business in Europe, the Middle East, and The Commonwealth
of Independent States, and the expansion into new markets and
geographies. Operating expenses are expected to increase during the
fourth quarter of 2012 and into 2013, driven by increased research and
development expenses associated with the planned clinical trials and
in-vitro studies to support potential regulatory approval of the
INTERCEPT red blood cell system. In addition, the Company expects to
incur additional regulatory costs in 2013 in connection with the planned
submission to the FDA of the modular PMA for INTERCEPT plasma in the
United States.
Operating and Net Income (Loss)
Operating losses during the third quarter of 2012 were $4.3 million,
compared to $2.7 million for the third quarter of 2011. Operating losses
during the first nine months of 2012 were $13.7 million, compared to
$12.6 million for the first nine months of 2011.
Net loss for the third quarter of 2012 was $3.5 million, or $0.08 per
diluted share, compared to a net income of $2.3 million, or $0.05 per
diluted share, for the third quarter of 2011. Net loss for the first
nine months of 2012 was $14.2 million, or $0.26 per diluted share,
compared to a net loss of $9.2 million, or $0.19 per diluted share, for
the first nine months of 2011. Net income and losses were impacted by
the mark-to-market adjustments of Cerus’ outstanding warrants to fair
value, which resulted in non-cash gains of $0.9 million and $5.4 million
during the three months ended September 30, 2012, and 2011,
respectively, and $0.1 million and $3.8 million during the nine months
ended September 30, 2012, and 2011, respectively.
Cash and Investments
At September 30, 2012, the Company had cash, cash equivalents and
short-term investments of $26.7 million. For the third quarter, tight
management of working capital, including accounts receivable and
payables, was instrumental in ending the quarter with lower cash used
for operations as compared to each of the first two quarters of 2012.
QUARTERLY CONFERENCE CALL
The Company will host a conference call and webcast at 4:15 p.m. Eastern
time today to discuss its financial results and provide a general
business overview and outlook. To access the live webcast, please visit
the Investor Relations page of the Cerus web site at http://www.cerus.com/Investors/Investor-Overview.
Alternatively, you may access the live conference call by dialing
866-235-9006 (U.S.) or 631-291-4549 (international).
A replay will be available on the company’s web site, or by dialing
855-859-2056 (U.S.) or 404-537-3406 (international) and entering
conference ID number 63119758. The replay will be available
approximately three hours after the call through November 21, 2012.
ABOUT CERUS
Cerus Corporation is a biomedical products company focused on
commercializing the INTERCEPT Blood System to enhance blood safety. The
INTERCEPT system is designed to reduce the risk of
transfusion-transmitted diseases by inactivating a broad range of
pathogens such as viruses, bacteria and parasites that may be present in
donated blood. The nucleic acid targeting mechanism of action enables
INTERCEPT treatment to inactivate established transfusion threats, such
as hepatitis B and C, HIV, West Nile virus and bacteria, and is designed
to inactivate emerging pathogens such as influenza, malaria and dengue.
Cerus currently markets and sells the INTERCEPT Blood System for both
platelets and plasma in Europe, The Commonwealth of Independent States,
the Middle East and selected countries in other regions around the
world. The INTERCEPT Blood System for red blood cells is in clinical
development. See http://www.cerus.com
for more information.
INTERCEPT and the INTERCEPT Blood System are trademarks of Cerus
Corporation.
Forward-Looking Statements
Except for the historical statements contained herein, this press
release contains forward-looking statements concerning Cerus’ products,
prospects and results, including statements concerning Cerus’
expectations regarding its 2012 revenue guidance, future operating
expenses and cash used to support operations, statements relating to the
planned submission of a modular PMA to the FDA for the INTERCEPT Blood
System for plasma, including the timing thereof, the sufficiency of
existing clinical data to enable a modular PMA submission and the
possibility of obtaining an early resolution of PMA deficiencies if
identified by the FDA, prospects for regulatory approvals of the
Company’s products and other future regulatory matters, and statements
relating to planned preparation and initiation of clinical trials and
the timing thereof, and the future development of the INTERCEPT Blood
System for red blood cells. Actual results could differ materially from
these forward-looking statements as a result of certain factors,
including, without limitation, risks associated with the
commercialization and market acceptance of, and customer demand for, the
INTERCEPT Blood System, the uncertain and time-consuming clinical
development and regulatory process, including the risks that planned
clinical trials for the INTERCEPT Blood System for red blood cells may
not occur on the timeframe discussed herein or otherwise in a timely
manner, or at all, that Cerus may be unable to reach agreement with the
FDA on the planned modular PMA submission for the INTERCEPT Blood System
for plasma or may be required to conduct additional clinical development
of the plasma system, and that if additional clinical development of the
plasma system is required it may be impractical to perform or require
funding that Cerus does not currently have, adverse market and economic
conditions, adverse fluctuations in foreign exchange rates, Cerus’
reliance on third parties to market, sell, distribute and maintain its
products, Cerus’ ability to maintain an effective manufacturing supply
chain, intellectual property protection, as well as other risks detailed
in Cerus’ filings with the Securities and Exchange Commission, including
Cerus’ Quarterly Report on Form 10-Q for the quarter ended June 30, 2012
filed with the SEC on August 8, 2012. Cerus disclaims any obligation or
undertaking to update or revise any forward-looking statements contained
in this press release.
|
CERUS CORPORATION
CONDENSED CONSOLIDATED UNAUDITED STATEMENTS OF OPERATIONS
(in thousands except per share information)
|
|
|
|
|
|
|
|
Three Months Ended
September 30,
|
|
Nine Months Ended
September 30,
|
|
|
|
2012
|
|
|
|
2011
|
|
|
|
2012
|
|
|
|
2011
|
|
|
Revenue:
|
|
|
|
|
|
|
|
|
Product revenue
|
$
|
8,252
|
|
|
$
|
7,770
|
|
|
$
|
26,167
|
|
|
$
|
20,706
|
|
|
Government grant and cooperative agreements
|
|
--
|
|
|
|
1,479
|
|
|
|
91
|
|
|
|
1,915
|
|
|
Total revenue
|
|
8,252
|
|
|
|
9,249
|
|
|
|
26,258
|
|
|
|
22,621
|
|
|
|
|
|
|
|
|
|
|
|
Cost of product revenue
|
|
4,411
|
|
|
|
4,726
|
|
|
|
15,499
|
|
|
|
12,329
|
|
|
Gross profit
|
|
3,841
|
|
|
|
4,523
|
|
|
|
10,759
|
|
|
|
10,292
|
|
|
|
|
|
|
|
|
|
|
|
Operating expenses:
|
|
|
|
|
|
|
|
|
Research and development
|
|
1,903
|
|
|
|
1,814
|
|
|
|
5,439
|
|
|
|
5,616
|
|
|
Selling, general and administrative
|
|
6,219
|
|
|
|
5,380
|
|
|
|
18,871
|
|
|
|
17,115
|
|
|
Amortization of intangible assets
|
|
50
|
|
|
|
51
|
|
|
|
151
|
|
|
|
152
|
|
|
Total operating expenses
|
|
8,172
|
|
|
|
7,245
|
|
|
|
24,461
|
|
|
|
22,883
|
|
|
Loss from operations
|
|
(4,331
|
)
|
|
|
(2,722
|
)
|
|
|
(13,702
|
)
|
|
|
(12,591
|
)
|
|
Non-operating income (expense), net
|
|
871
|
|
|
|
4,982
|
|
|
|
(499
|
)
|
|
|
3,344
|
|
|
|
|
|
|
|
|
|
|
|
Net income (loss)
|
$
|
(3,460
|
)
|
|
$
|
2,260
|
|
|
$
|
(14,201
|
)
|
|
$
|
(9,247
|
)
|
|
|
|
|
|
|
|
|
|
|
Net income (loss) per common share:
|
|
|
|
|
|
|
|
|
Basic
|
$
|
(0.06
|
)
|
|
$
|
0.05
|
|
|
$
|
(0.26
|
)
|
|
$
|
(0.19
|
)
|
|
Diluted
|
$
|
(0.08
|
)
|
|
$
|
0.05
|
|
|
$
|
(0.26
|
)
|
|
$
|
(0.19
|
)
|
|
|
|
|
|
|
|
|
|
|
Weighted average common shares outstanding used for
|
|
|
|
|
|
|
|
|
computing net income (loss) per common share:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic
|
|
54,875
|
|
|
|
47,710
|
|
|
|
54,130
|
|
|
|
47,600
|
|
|
Diluted
|
|
55,377
|
|
|
|
48,820
|
|
|
|
54,130
|
|
|
|
47,600
|
|
|
CERUS CORPORATION
CONDENSED CONSOLIDATED UNAUDITED BALANCE SHEETS
(in thousands)
|
|
|
|
|
|
|
|
|
|
|
|
September 30,
2012
|
|
December 31,
2011
|
|
|
|
|
|
|
|
|
Cash, cash equivalents, and short-term investments
|
|
|
$
|
26,661
|
|
$
|
25,784
|
|
Accounts receivable and other current assets
|
|
|
|
7,193
|
|
|
7,511
|
|
Inventories
|
|
|
|
9,682
|
|
|
6,444
|
|
Property and equipment, net
|
|
|
|
1,801
|
|
|
2,032
|
|
Goodwill and intangible assets
|
|
|
|
2,913
|
|
|
3,064
|
|
Other assets
|
|
|
|
403
|
|
|
532
|
|
Total assets
|
|
|
$
|
48,653
|
|
$
|
45,367
|
|
|
|
|
|
|
|
|
Accounts payable and accrued liabilities
|
|
|
$
|
13,787
|
|
$
|
10,505
|
|
Deferred revenue
|
|
|
|
716
|
|
|
111
|
|
Debt - current
|
|
|
|
4,919
|
|
|
2,519
|
|
Warrant liability
|
|
|
|
7,876
|
|
|
7,979
|
|
Debt - non-current
|
|
|
|
3,307
|
|
|
4,697
|
|
Other non-current liabilities
|
|
|
|
1,132
|
|
|
1,243
|
|
Total liabilities
|
|
|
|
31,737
|
|
|
27,054
|
|
Stockholders’ equity
|
|
|
|
16,916
|
|
|
18,313
|
|
Total liabilities and stockholders’ equity
|
|
|
$
|
48,653
|
|
$
|
45,367
|

Source: Cerus Corporation