UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): February 28, 2008 (February 27, 2008)
REGENERON PHARMACEUTICALS, INC.
(Exact Name of Registrant as Specified in Charter)
| New York | 000-19034 | 13-3444607 | ||
| (State or other jurisdiction of | (Commission File No.) | (IRS Employer Identification No.) | ||
| Incorporation) |
777 Old Saw Mill River Road, Tarrytown, New York 10591-6707
(Address of principal executive offices, including zip code)
(914) 347-7000
(Registrant’s telephone number, including area code)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the
filing obligation of the registrant under any of the following provisions:
| o | Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
| o | Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| o | Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| o | Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Item 2.02 Results of Operations and Financial Condition.
On February 27, 2008, Regeneron Pharmaceuticals, Inc. issued a press release announcing its
financial and operating results for the fourth quarter and full year ended December 31, 2007. The
press release is being furnished to the Securities and Exchange Commission pursuant to Item 2.02 of
Form 8-K and is attached as Exhibit 99.1 to this Form 8-K.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits
99.1
|
Press Release dated February 27, 2008. |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly
caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
| Date: February 28, 2008 | REGENERON PHARMACEUTICALS, INC. |
|||
| By: | /s/ Stuart Kolinski | |||
| Name: | Stuart Kolinski | |||
| Title: | Senior Vice President and General Counsel |
|||
Exhibit Index
| Number | Description | |
99.1
|
Press Release dated February 27, 2008. |
Exhibit 99.1
FOR IMMEDIATE RELEASE
Press Release
Regeneron Reports Fourth Quarter and Full Year 2007 Financial and Operating Results
Tarrytown, New York (February 27, 2008) — Regeneron Pharmaceuticals, Inc. (Nasdaq: REGN) today
announced financial and operating results for the fourth quarter and full year 2007. The Company
reported a net loss of $13.1 million, or $0.19 per share (basic and diluted), for the fourth
quarter of 2007 compared with a net loss of $31.0 million, or $0.51 per share (basic and diluted),
for the fourth quarter of 2006. The Company reported a net loss of $105.6 million, or $1.59 per
share (basic and diluted), for the year ended December 31, 2007 compared with a net loss of $102.3
million, or $1.77 per share (basic and diluted), for the same period in 2006. In the fourth
quarter of 2007, in connection with the Company’s VEGF Trap-Eye collaboration with Bayer
HealthCare, the Company recognized a cumulative catch-up of $35.9 million of contract research and
development revenue and $10.6 million of additional research and development expense, as described
below.
At December 31, 2007, cash, restricted cash, and marketable securities totaled $846.3 million
compared with $522.9 million at December 31, 2006. In November 2007, the Company and the
sanofi-aventis Group entered into a global, strategic collaboration to discover, develop, and
commercialize fully human monoclonal antibodies and sanofi-aventis made an $85.0 million up-front
payment to Regeneron. In addition, in December 2007, sanofi-aventis purchased 12 million newly
issued shares of Regeneron Common Stock at $26.00 per share for proceeds to the Company of $312.0
million.
The Company’s $200.0 million of convertible notes, which bear interest at 5.5 percent per annum,
mature in October 2008.
Current Business Highlights
Regeneron has three late-stage clinical development programs: ARCALYST™ (rilonacept; also known as IL-1 Trap) in Cryopyrin-Associated Periodic Syndromes (CAPS), aflibercept (the VEGF Trap) in oncology in collaboration with the sanofi-aventis Group, and the VEGF Trap-Eye in eye diseases in collaboration with Bayer HealthCare. Regeneron has also initiated a Phase 2 trial of ARCALYST™ for the prevention of gout.
Regeneron has three late-stage clinical development programs: ARCALYST™ (rilonacept; also known as IL-1 Trap) in Cryopyrin-Associated Periodic Syndromes (CAPS), aflibercept (the VEGF Trap) in oncology in collaboration with the sanofi-aventis Group, and the VEGF Trap-Eye in eye diseases in collaboration with Bayer HealthCare. Regeneron has also initiated a Phase 2 trial of ARCALYST™ for the prevention of gout.
In addition, Regeneron has commenced a Phase 1 trial of its first fully human monoclonal antibody
candidate, REGN88, an antibody targeting the interleukin-6 receptor
(IL-6R) in
rheumatoid arthritis, as part of its antibody collaboration with sanofi-aventis. The Company is developing a
pipeline of preclinical antibody candidates utilizing its VelocImmuneÒ
technology.
Regeneron achieved the following milestones in the fourth quarter of 2007:
| • | Entered into a global, strategic collaboration agreement with sanofi-aventis to discover, develop, and commercialize fully human monoclonal antibodies. | ||
| • | Reported extended safety results from a Phase 3 trial of ARCALYST™ in patients with CAPS at the American College of Rheumatology (ACR) Annual Meeting in November 2007. | ||
| • | Initiated a Phase 2 safety and efficacy trial of ARCALYST™ in the prevention of gout flares. | ||
| • | Reported positive results from the extension phase of the Phase 2 trial of the VEGF Trap-Eye in age-related macular degeneration (wet AMD). | ||
| • | Initiation by sanofi-aventis of the third and fourth Phase 3 oncology trials for aflibercept in combination with standard chemotherapy regimens. | ||
| • | Initiated a Phase 1 clinical trial of REGN88 in rheumatoid arthritis. |
ARCALYST™ (rilonacept; also known as IL-1 Trap) — Inflammatory Diseases
The Company announced in November 2007 that the action date for the FDA’s priority review of the Biologics License Application (BLA) for ARCALYST™ for the long-term treatment of CAPS was set for February 29, 2008. CAPS is a group of rare inherited inflammatory conditions, including Familial Cold Auto-inflammatory Syndrome and Muckle-Wells Syndrome. The FDA previously granted Orphan Drug status and Fast Track designation to ARCALYST™ for the treatment of CAPS. ARCALYST™ has also received Orphan Drug designation in the European Union for the treatment of CAPS.
The Company announced in November 2007 that the action date for the FDA’s priority review of the Biologics License Application (BLA) for ARCALYST™ for the long-term treatment of CAPS was set for February 29, 2008. CAPS is a group of rare inherited inflammatory conditions, including Familial Cold Auto-inflammatory Syndrome and Muckle-Wells Syndrome. The FDA previously granted Orphan Drug status and Fast Track designation to ARCALYST™ for the treatment of CAPS. ARCALYST™ has also received Orphan Drug designation in the European Union for the treatment of CAPS.
In the fourth quarter, Regeneron initiated a Phase 2 safety and efficacy trial of ARCALYST™ in the
prevention of gout flares induced by the initiation of uric acid-lowering drug therapy used to
control the disease. The Company had previously reported positive results from an exploratory
proof-of-concept study of ARCALYST™ in ten patients with chronic active gout. In those patients,
treatment with ARCALYST™ demonstrated a statistically significant reduction in patient pain scores
in the single-blind, placebo-controlled study. Mean patients’ pain scores, the key symptom measure
in persistent gout, were reduced 41 percent (p=0.025) during the first two weeks of active
treatment and reduced 56 percent (p<0.004) after six weeks of active treatment. In this study,
in which safety was the primary endpoint measure, treatment with ARCALYST™ was generally
well-tolerated. Regeneron is evaluating the potential use of ARCALYST™ in other indications in
which interleukin-1 (IL-1) may play a role.
Aflibercept (VEGF Trap) — Oncology
In December 2007, Regeneron and sanofi-aventis announced the initiation of the third and fourth Phase 3 trials in oncology that combine aflibercept with standard chemotherapy regimens. One trial is evaluating aflibercept in combination with folinic acid, 5-FU, and irinotecan in patients with 2nd line metastatic colorectal cancer. The other trial is evaluating aflibercept in combination with gemcitabine in patients with 1st line metastatic pancreatic cancer. In the first two Phase 3
In December 2007, Regeneron and sanofi-aventis announced the initiation of the third and fourth Phase 3 trials in oncology that combine aflibercept with standard chemotherapy regimens. One trial is evaluating aflibercept in combination with folinic acid, 5-FU, and irinotecan in patients with 2nd line metastatic colorectal cancer. The other trial is evaluating aflibercept in combination with gemcitabine in patients with 1st line metastatic pancreatic cancer. In the first two Phase 3
trials initiated by the collaboration, aflibercept is being evaluated in
combination with docetaxel/prednisone in patients with 1st line metastatic androgen
independent prostate cancer and in combination with docetaxel in patients with 2nd line
metastatic non-small cell lung cancer. All four trials are studying the current standard of
chemotherapy care for the cancer being studied with or without aflibercept. In addition, currently underway are 10 studies being conducted in
conjunction with the National Cancer Institute (NCI) Cancer Therapy Evaluation Program (CTEP)
evaluating aflibercept as a single agent or in combination with chemotherapy regimens in a variety
of cancer indications.
VEGF Trap-Eye — Eye Diseases
The VEGF Trap-Eye is a specially purified and formulated form of the VEGF Trap for use in intraocular applications. Regeneron and Bayer HealthCare initiated a Phase 3 global development program of the VEGF Trap-Eye in wet AMD in the third quarter of 2007. The first trial, known as VIEW 1 (VEGF Trap: Investigation of Efficacy and Safety in Wet age-related macular degeneration), is comparing the VEGF Trap-Eye and Genentech, Inc.’s Lucentisâ (ranibizumab), an anti-angiogenic agent approved for use in wet AMD. The trial is evaluating dosing intervals of four and eight weeks for the VEGF Trap-Eye, compared with ranibizumab dosed every four weeks according to its label. Regeneron and Bayer HealthCare plan to initiate a second Phase 3 trial in wet AMD in the first half of 2008. This second trial will be conducted primarily in the European Union and other parts of the world outside the U.S.
The VEGF Trap-Eye is a specially purified and formulated form of the VEGF Trap for use in intraocular applications. Regeneron and Bayer HealthCare initiated a Phase 3 global development program of the VEGF Trap-Eye in wet AMD in the third quarter of 2007. The first trial, known as VIEW 1 (VEGF Trap: Investigation of Efficacy and Safety in Wet age-related macular degeneration), is comparing the VEGF Trap-Eye and Genentech, Inc.’s Lucentisâ (ranibizumab), an anti-angiogenic agent approved for use in wet AMD. The trial is evaluating dosing intervals of four and eight weeks for the VEGF Trap-Eye, compared with ranibizumab dosed every four weeks according to its label. Regeneron and Bayer HealthCare plan to initiate a second Phase 3 trial in wet AMD in the first half of 2008. This second trial will be conducted primarily in the European Union and other parts of the world outside the U.S.
In the fourth quarter of 2007, the companies announced positive results of the Phase 2 trial of the
VEGF Trap-Eye in wet AMD. The VEGF Trap-Eye met the primary study endpoint of a statistically
significant reduction in retinal thickness, a measure of disease activity, after 12 weeks of
treatment compared with baseline (all five dose groups combined, mean decrease of 119 microns,
p<0.0001). In additional exploratory analyses, the VEGF Trap-Eye, dosed monthly, demonstrated
improvements in visual acuity. The VEGF Trap-Eye reduced the proportion of patients with vision of
20/200 or worse (a generally accepted definition for legal blindness), from 14.3 percent at
baseline to 1.6 percent at week 16. In a separate analysis, the proportion of patients with vision
of 20/40 or better (part of the legal minimum requirement for an unrestricted driver’s license in
the U.S.) was increased from 19.0 percent at baseline to 49.2 percent at 16 weeks.
Regeneron and Bayer HealthCare are collaborating on the global development of the VEGF Trap-Eye for
the treatment of wet AMD, diabetic eye diseases, and other eye diseases and disorders. Bayer
HealthCare will market the VEGF Trap-Eye outside the United States, where the companies will share
equally in profits from any future sales of the VEGF Trap-Eye. Regeneron maintains exclusive rights
to the VEGF Trap-Eye in the United States.
Monoclonal Antibodies
In the fourth quarter of 2007, Regeneron and sanofi-aventis entered into a global, strategic collaboration agreement to discover, develop, and commercialize fully human monoclonal antibodies. The first therapeutic antibody to enter clinical development under the collaboration, REGN88, is an antibody to the Interleukin-6 receptor (IL-6R), which has started clinical trials in rheumatoid arthritis. The second is expected to be an antibody to Delta-like ligand-4 (Dll4),
In the fourth quarter of 2007, Regeneron and sanofi-aventis entered into a global, strategic collaboration agreement to discover, develop, and commercialize fully human monoclonal antibodies. The first therapeutic antibody to enter clinical development under the collaboration, REGN88, is an antibody to the Interleukin-6 receptor (IL-6R), which has started clinical trials in rheumatoid arthritis. The second is expected to be an antibody to Delta-like ligand-4 (Dll4),
which is currently slated to start clinical development in mid-2008. Regeneron plans to advance two
antibody product candidates into clinical development in 2008 and an additional two to three
antibody product candidates each year thereafter beginning in 2009.
The collaboration is governed by a Discovery and Preclinical Development Agreement and a License
and Collaboration Agreement. As part of the discovery agreement, sanofi-aventis made an $85.0
million up-front payment to Regeneron. In addition, sanofi-aventis agreed to fund up to $475.0
million of research over the next five years to identify and validate potential drug discovery
targets and to develop fully human monoclonal antibodies against these targets. Sanofi-aventis has
an option to extend the discovery agreement for up to an additional three years.
Sanofi-aventis has the exclusive option under the license agreement to co-develop antibodies
arising from Regeneron’s discovery efforts. Sanofi-aventis will fund the drug candidate
development costs up-front and Regeneron will reimburse sanofi-aventis for half of the development
costs from its share of future antibody profits from the collaboration.
For any product successfully developed as part of the collaboration, sanofi-aventis will take the
lead in commercialization activities and Regeneron has worldwide co-promotion rights. In the
United States, profits and losses from sales of collaboration antibodies will be shared equally.
Outside the United States, profits will be split on a pre-determined sliding scale based on
aggregate sales of collaboration antibodies with Regeneron’s’ share ranging from 35 percent to 45
percent. Regeneron is responsible for 45 percent of losses outside the United States. In
addition, Regeneron is entitled to receive up to a total of $250.0 million of sales milestone
payments when the collaboration antibodies achieve certain aggregate annual ex-U.S. sales levels,
starting at $1.0 billion.
In December 2007, sanofi-aventis also increased its ownership of Regeneron’s outstanding Common
Stock from approximately 4 percent to approximately 19 percent by purchasing 12 million newly
issued shares of Regeneron Common Stock at $26.00 per share for proceeds to the Company of $312.0
million.
Earlier in 2007, Regeneron entered into non-exclusive license agreements with AstraZeneca and
Astellas that will allow those companies to utilize VelocImmune technology in their internal
research programs to discover human monoclonal antibody product candidates. Each of those
companies made a $20.0 million up-front, non-refundable payment and will make up to five additional
annual payments of $20.0 million, subject to the ability to terminate the agreement after making
the first three additional payments. Upon commercialization of any antibody products discovered
utilizing VelocImmune, the licensees will pay to Regeneron a mid-single-digit royalty on product
sales.
Financial Results
Revenue
Regeneron’s total revenue increased to $64.7 million in the fourth quarter of 2007 from $10.3 million in the same quarter of 2006 and to $125.0 million for the full year 2007 from $63.4 million for the same period of 2006. Contract research and development revenue in the first three quarters of 2007 and the full-year 2006 principally related to the Company’s aflibercept collaboration with
Revenue
Regeneron’s total revenue increased to $64.7 million in the fourth quarter of 2007 from $10.3 million in the same quarter of 2006 and to $125.0 million for the full year 2007 from $63.4 million for the same period of 2006. Contract research and development revenue in the first three quarters of 2007 and the full-year 2006 principally related to the Company’s aflibercept collaboration with
sanofi-aventis in cancer indications. In the fourth quarter of 2007, the Company also recognized
contract research and development revenue from the Company’s VEGF Trap-Eye collaboration with Bayer
HealthCare and its new collaboration with sanofi-aventis to discover, develop, and commercialize
fully human monoclonal antibodies. Contract manufacturing revenue in 2006
related to Regeneron’s long-term manufacturing agreement with Merck & Co., Inc., which expired in
October 2006. Technology licensing revenue in 2007 related to the Company’s license agreements
with AstraZeneca and Astellas.
Regeneron recognized contract research and development revenue of $12.6 million in the fourth
quarter of 2007 and $47.1 million for the full year 2007 related to the Company’s aflibercept
collaboration with sanofi-aventis, compared with $9.1 million and $47.8 million, respectively, for
the same periods of 2006. Contract research and development revenue from the collaboration
consisted of reimbursement of aflibercept development expenses incurred by the Company plus
recognition of amounts related to $105.0 million of previously received and deferred
non-refundable, up-front payments. Reimbursement of expenses increased to $10.5 million in the
fourth quarter of 2007 and to $38.3 million for the full year 2007 from $6.8 million and $36.4
million, respectively, in the comparable periods of 2006, principally due to higher preclinical and
clinical development costs and, in the fourth quarter of 2007, higher costs related to the
Company’s manufacture of aflibercept clinical supplies. With respect to the $105.0 million of
up-front payments from sanofi-aventis, $2.1 million was recognized in the fourth quarter of 2007
compared to $2.2 million in the same quarter of 2006, and $8.8 million was recognized in the full
year 2007 compared to $11.4 million in the same period of 2006.
Sanofi-aventis also incurs aflibercept development expenses directly and these expenses are
increasing because of the growing number of clinical trials sanofi-aventis is overseeing in the
aflibercept oncology program. During the term of the aflibercept collaboration, sanofi-aventis
pays 100 percent of agreed-upon aflibercept development expenses incurred by both companies.
Following commercialization of an aflibercept product, Regeneron, from its 50 percent share of
aflibercept profits, will reimburse sanofi-aventis for 50 percent of aflibercept development
expenses previously paid by sanofi-aventis.
In connection with the Company’s VEGF Trap-Eye collaboration with Bayer HealthCare, the Company
received a $75.0 million non-refundable, up-front payment in October 2006 and a $20.0 million
milestone payment in August 2007. Through September 30, 2007, all payments received from Bayer
HealthCare, including the up-front and milestone payments and cost-sharing reimbursements, were
fully deferred and included in deferred revenue. In the fourth quarter of 2007, the Company
commenced recognizing previously deferred payments from Bayer HealthCare and cost-sharing of the
Company’s and Bayer HealthCare’s 2007 VEGF Trap-Eye development expenses in the Company’s Statement
of Operations through a cumulative catch-up. The $75.0 million non-refundable, up-front license
payment and $20.0 million milestone payment are being recognized as contract research and
development revenue over the related estimated performance period in accordance with Staff
Accounting Bulletin No. 104, Revenue Recognition (SAB 104) and Emerging Issues Task Force 00-21,
Accounting for Revenue Arrangements with Multiple Deliverables (EITF 00-21). In periods when the
Company recognizes VEGF Trap-Eye development expenses that it incurs under the collaboration, the
Company also recognizes, as
contract research and development revenue, the portion of those VEGF
Trap-Eye development expenses that are reimbursable from Bayer HealthCare. In periods when Bayer
HealthCare incurs agreed upon VEGF Trap-Eye development expenses that benefit the collaboration and
Regeneron, the Company also recognizes, as additional research and development expense, the portion
of Bayer HealthCare’s VEGF Trap-Eye development expenses that the Company is obligated to reimburse.
In the fourth quarter of 2007, the Company recorded a cumulative catch-up of $35.9 million of
contract research and development revenue from Bayer HealthCare, consisting of (i) $15.9 million
related to the $75.0 million up-front licensing payment and the $20.0 million milestone payment and
(ii) $20.0 million related to the portion of the Company’s 2007 VEGF Trap-Eye development expenses
that is reimbursable from Bayer HealthCare. In addition, in the fourth quarter of 2007, the
Company recorded a cumulative catch-up of $10.6 million of additional research and development
expense related to the portion of Bayer HealthCare’s 2007 VEGF Trap-Eye development expenses that
the Company was obligated to reimburse.
In connection with the Company’s antibody collaboration with sanofi-aventis, the Company recognized
$4.6 million of contract research and development revenue in the fourth quarter of 2007, which
consisted of $3.0 million for reimbursement of the Company’s expenses under the collaboration’s
discovery agreement, $0.7 million for reimbursement of the Company’s REGN88 development expenses,
and $0.9 million related to the $85.0 million non-refundable, up-front payment, which was deferred
upon receipt in December 2007. Contract research and development revenue in connection with the
antibody collaboration with sanofi-aventis is being recognized in accordance with SAB 104 and EITF
00-21.
Contract research and development revenue also includes $1.0 million in the fourth quarter of 2007
and $5.5 million for the full year 2007, compared to $0.4 million and $0.5 million, respectively,
for the same periods of 2006, in connection with the Company’s five-year grant from the National
Institutes of Health (NIH), which was awarded to the Company in September 2006 as part of the NIH’s
Knockout Mouse Project.
In connection with the Company’s license agreements with AstraZeneca and Astellas, both of the
$20.0 million non-refundable, up-front payments received in February and April 2007, respectively,
were deferred and are being recognized as revenue ratably over approximately the first year of each
agreement. In the fourth quarter and for the full year 2007, the Company recognized $10.0 million
and $28.4 million, respectively, of technology licensing revenue related to these agreements.
Expenses
Total operating expenses for the fourth quarter of 2007 were $76.3 million, 74 percent higher than the same period in 2006, and $239.5 million for the full year 2007, 40 percent higher than for the same period of 2006. Operating expenses included non-cash compensation expense related to employee stock option awards (Stock Option Expense) of $7.5 million in the fourth quarter of 2007 and $28.0 million for the full year 2007, compared with $5.1 million and $18.4 million, respectively, for the same periods of 2006. The increase in total Stock Option Expense in 2007
Total operating expenses for the fourth quarter of 2007 were $76.3 million, 74 percent higher than the same period in 2006, and $239.5 million for the full year 2007, 40 percent higher than for the same period of 2006. Operating expenses included non-cash compensation expense related to employee stock option awards (Stock Option Expense) of $7.5 million in the fourth quarter of 2007 and $28.0 million for the full year 2007, compared with $5.1 million and $18.4 million, respectively, for the same periods of 2006. The increase in total Stock Option Expense in 2007
was primarily due to the higher fair market value of the Company’s Common Stock on the date of annual employee option grants
made by the Company in December 2006 in comparison to the fair market value of the Company’s Common
Stock on the dates of annual employee option grants made in recent prior years.
Research and development (R&D) expenses increased to $64.8 million in the fourth quarter of 2007
from $35.8 million in the comparable quarter of 2006, and to $201.6 million for the full year 2007
from $137.1 million for the same period of 2006. In addition to the impact of Stock Option
Expense, as described above, in 2007, the Company incurred higher R&D costs primarily related to
additional R&D headcount, clinical development costs for the VEGF Trap-Eye and ARCALYST™, research
and preclinical development costs for new antibody candidates, and costs to manufacture clinical
supplies of ARCALYST™ and REGN88. Also, as described above, in the fourth quarter of 2007, the
Company recorded a cumulative catch-up of $10.6 million of additional research and development
expense related to the Company’s VEGF Trap-Eye collaboration with Bayer HealthCare.
General and administrative (G&A) expenses increased to $11.4 million in the fourth quarter of 2007
from $7.6 million in the comparable quarter of 2006, and to $37.9 million in the full year 2007
from $25.9 million in the same period of 2006. In addition to the impact of Stock Option Expense,
as described above, in 2007, the Company incurred higher compensation expense due, in part, to
additional headcount, higher recruitment and related costs associated with expanding the Company’s
headcount in 2007, and higher fees for various professional services.
Other Income
Investment income decreased to $1.5 million in the fourth quarter of 2007 from $5.5 million in the comparable quarter of 2006, and increased to $20.9 million for the full year 2007 from $16.5 million for the same period of 2006. In the fourth quarter and for the full year 2007, the Company recognized $5.1 million and $5.9 million, respectively, in charges related to certain marketable securities that were determined to be other-than-temporarily impaired in value. For the full-year 2007, the increase in investment income resulted primarily from higher balances of cash and marketable securities due, in part, to the up-front payment received from Bayer HealthCare in October 2006 and the receipt of $174.6 million in net proceeds from the November 2006 public offering of 7.6 million shares of the Company’s Common Stock, partly offset by the impairment charges previously described.
Investment income decreased to $1.5 million in the fourth quarter of 2007 from $5.5 million in the comparable quarter of 2006, and increased to $20.9 million for the full year 2007 from $16.5 million for the same period of 2006. In the fourth quarter and for the full year 2007, the Company recognized $5.1 million and $5.9 million, respectively, in charges related to certain marketable securities that were determined to be other-than-temporarily impaired in value. For the full-year 2007, the increase in investment income resulted primarily from higher balances of cash and marketable securities due, in part, to the up-front payment received from Bayer HealthCare in October 2006 and the receipt of $174.6 million in net proceeds from the November 2006 public offering of 7.6 million shares of the Company’s Common Stock, partly offset by the impairment charges previously described.
About Regeneron Pharmaceuticals
Regeneron is a biopharmaceutical company that discovers, develops, and intends to commercialize therapeutic medicines for the treatment of serious medical conditions. Regeneron has therapeutic candidates in clinical trials for the potential treatment of cancer, eye diseases, and inflammatory diseases, and has preclinical programs in other diseases and disorders.
Regeneron is a biopharmaceutical company that discovers, develops, and intends to commercialize therapeutic medicines for the treatment of serious medical conditions. Regeneron has therapeutic candidates in clinical trials for the potential treatment of cancer, eye diseases, and inflammatory diseases, and has preclinical programs in other diseases and disorders.
This news release discusses historical information and includes forward-looking statements about
Regeneron and its products, programs, finances, and business, all of which involve a number of
risks and uncertainties, such as risks associated with preclinical and clinical development of our
drug candidates, determinations by regulatory and administrative governmental authorities which may
delay or restrict our ability to continue to develop or commercialize our drug candidates,
competing drugs that are superior to our product candidates, unanticipated expenses, the
availability and cost of capital, the costs of developing, producing, and selling products, the
potential for any collaboration agreement, including our agreements with the sanofi-aventis Group
and Bayer
HealthCare, to be canceled or to terminate without any product success, risks associated
with third party intellectual property, and other material risks. A more complete description of
these and other material risks can be found in Regeneron’s filings with the United States
Securities and Exchange Commission (SEC), including its Form 10-K for the year ended December 31,
2006 and Form 10-Q for the quarter ended September 30, 2007. Regeneron does not undertake any
obligation to update publicly any forward-looking statement, whether as a result of new
information, future events, or otherwise unless required by law.
###
Contacts Information: |
||
Charles Poole |
Laura Lindsay | |
Investor Relations |
Media Relations | |
914.345.7640 |
914.345.7800 | |
charles.poole@regeneron.com |
laura.lindsay@regeneron.com | |
| Kimberly Chen | ||
| Media Relations | ||
| 212.845.5634 | ||
| kchen@biosector2.com |
REGENERON PHARMACEUTICALS, INC.
CONDENSED BALANCE SHEETS (Unaudited)
(In thousands)
CONDENSED BALANCE SHEETS (Unaudited)
(In thousands)
| December 31, | December 31, | |||||||
| 2007 | 2006 | |||||||
ASSETS |
||||||||
Cash, restricted cash, and marketable securities |
$ | 846,279 | $ | 522,859 | ||||
Receivables |
18,320 | 7,493 | ||||||
Property, plant, and equipment, net |
58,304 | 49,353 | ||||||
Other assets |
13,355 | 5,385 | ||||||
Total assets |
$ | 936,258 | $ | 585,090 | ||||
LIABILITIES AND STOCKHOLDERS’ EQUITY |
||||||||
Accounts payable and accrued expenses |
$ | 39,232 | $ | 21,471 | ||||
Deferred revenue |
236,759 | 146,995 | ||||||
Notes payable |
200,000 | 200,000 | ||||||
Stockholders’ equity |
460,267 | 216,624 | ||||||
Total liabilities and stockholders’ equity |
$ | 936,258 | $ | 585,090 | ||||
REGENERON PHARMACEUTICALS, INC.
CONDENSED STATEMENTS OF OPERATIONS (Unaudited)
(In thousands, except per share data)
(In thousands, except per share data)
| For the three months | For the year | |||||||||||||||
| ended December 31, | ended December 31, | |||||||||||||||
| 2007 | 2006 | 2007 | 2006 | |||||||||||||
Revenues |
||||||||||||||||
Contract research and development |
$ | 54,730 | $ | 10,110 | $ | 96,603 | $ | 51,136 | ||||||||
Contract manufacturing |
236 | 12,311 | ||||||||||||||
Technology licensing |
10,000 | 28,421 | ||||||||||||||
| 64,730 | 10,346 | 125,024 | 63,447 | |||||||||||||
Expenses |
||||||||||||||||
Research and development |
64,825 | 35,774 | 201,613 | 137,064 | ||||||||||||
Contract manufacturing |
430 | 8,146 | ||||||||||||||
General and administrative |
11,439 | 7,628 | 37,865 | 25,892 | ||||||||||||
| 76,264 | 43,832 | 239,478 | 171,102 | |||||||||||||
Loss from operations |
(11,534 | ) | (33,486 | ) | (114,454 | ) | (107,655 | ) | ||||||||
Other income (expense) |
||||||||||||||||
Investment income |
1,473 | 5,525 | 20,897 | 16,548 | ||||||||||||
Interest expense |
(3,010 | ) | (3,010 | ) | (12,043 | ) | (12,043 | ) | ||||||||
| (1,537 | ) | 2,515 | 8,854 | 4,505 | ||||||||||||
Net loss before cumulative effect of a change in
accounting principle |
(13,071 | ) | (30,971 | ) | (105,600 | ) | (103,150 | ) | ||||||||
Cumulative effect of adopting Statement of Financial
Accounting Standards No. 123R (“SFAS 123R”) |
813 | |||||||||||||||
Net loss |
$ | (13,071 | ) | $ | (30,971 | ) | $ | (105,600 | ) | $ | (102,337 | ) | ||||
Net loss per share amounts, basic and diluted: |
||||||||||||||||
Net loss
before cumulative effect of a change in accounting principle |
$ | (0.19 | ) | $ | (0.51 | ) | $ | (1.59 | ) | $ | (1.78 | ) | ||||
Cumulative effect of adopting SFAS 123R |
0.01 | |||||||||||||||
Net loss |
$ | (0.19 | ) | $ | (0.51 | ) | $ | (1.59 | ) | $ | (1.77 | ) | ||||
Weighted average shares outstanding,
basic and diluted |
67,754 | 61,229 | 66,334 | 57,970 | ||||||||||||