UNITED STATES
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
| Date of Report (Date of earliest event reported): February 26, 2009 |
| 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 26, 2009, Regeneron Pharmaceuticals, Inc. issued a press release announcing its financial and operating results for the quarter and year ended December 31, 2008. 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 26, 2009.
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.
| REGENERON PHARMACEUTICALS, INC. | ||
| Date: February 26, 2009 | ||
| By: | /s/ Stuart Kolinski | |
| Name: Stuart Kolinski | ||
| Title: Senior Vice President and General | ||
| Counsel | ||
Exhibit Index
| Number | Description | ||
| 99.1 | Press Release dated February 26, 2009. | ||
Exhibit 99.1
For Immediate Release
| Press Release |
Regeneron Reports Full Year and Fourth
Quarter 2008
Financial and Operating Results
Tarrytown, New York (February 26, 2009) -- Regeneron Pharmaceuticals, Inc. (Nasdaq: REGN) today announced financial and operating results for the full year and fourth quarter 2008. The Company reported a net loss of $82.7 million, or $1.05 per share (basic and diluted), for the year ended December 31, 2008 compared with a net loss of $105.6 million, or $1.59 per share (basic and diluted), for the same period in 2007. The Company reported a net loss of $31.5 million, or $0.40 per share (basic and diluted), for the fourth quarter of 2008 compared with a net loss of $13.1 million, or $0.19 per share (basic and diluted), for the fourth quarter of 2007. 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 revenue and expenses that reduced the net loss for the quarter by $25.3 million, as described below.
At December 31, 2008, cash, restricted cash, and marketable securities totaled $527.5 million compared with $846.3 million at December 31, 2007. During 2008, the Company retired the full $200 million of its 5.5 percent Convertible Senior Subordinated Notes.
Current Business Highlights
ARCALYST® (rilonacept) – Inflammatory Diseases
The Company shipped $10.7 million of
ARCALYST® (rilonacept) Injection for
Subcutaneous Use to its distributors in 2008. In
February 2008, the Company received marketing approval from the U.S. Food and
Drug Administration (FDA) for ARCALYST for the treatment of Cryopyrin-Associated
Periodic Syndromes (CAPS), including Familial Cold Auto-inflammatory Syndrome
(FCAS) and Muckle-Wells Syndrome (MWS) in adults and children 12 and older.
ARCALYST, an interleukin-1 (IL-1) blocker, is the only therapy approved in the
United States for patients with CAPS, a group of rare, inherited,
auto-inflammatory conditions characterized by life-long, recurrent symptoms of
rash, fever/chills, joint pain, eye redness/pain, and fatigue. Intermittent,
disruptive exacerbations or flares can be triggered at any time by exposure to
cooling temperatures, stress, exercise, or other unknown stimuli.
In March 2008, ARCALYST became available for prescription in the United States, and the Company transitioned the patients who participated in the CAPS pivotal study from clinical study drug to commercial supplies. The Company currently projects shipments of ARCALYST to its distributors to total approximately $20-24 million in 2009.
The Company is in the process of initiating a Phase 3 clinical development program with ARCALYST for the treatment of gout. Two Phase 3 clinical trials will evaluate ARCALYST versus placebo for the prevention of gout flares in patients initiating urate-lowering drug therapy. The Company plans to initiate a Phase 3 clinical trial of ARCALYST for acute gout that will evaluate treatment with ARCALYST alone versus ARCALYST in combination with a non-steroidal anti-inflammatory drug (NSAID) versus an NSAID alone. The Phase 3 clinical development program will also include a separate safety study.
Aflibercept (VEGF Trap) –
Oncology
Regeneron and collaborator
sanofi-aventis are enrolling patients in four Phase 3 trials that combine
aflibercept, an anti-angiogenesis agent, with standard chemotherapy regimens for
the treatment of cancer. One trial is evaluating aflibercept as a
2nd line treatment for metastatic
colorectal cancer (the VELOUR study) in combination with FOLFIRI (folinic acid
(leucovorin), 5-fluorouracil, and irinotecan). A second trial is evaluating
aflibercept as a 1st line treatment
for metastatic pancreatic cancer in combination with gemcitabine (the VANILLA
study). A third trial is evaluating aflibercept as a 1st line treatment for metastatic androgen- independent prostate
cancer in combination with docetaxel/prednisone (the VENICE study). The fourth
trial is evaluating aflibercept as a 2nd line treatment for metastatic non-small cell lung cancer in combination
with docetaxel (the VITAL study). All four trials are studying the current
standard of chemotherapy care for the cancer being studied with and without
aflibercept. Each of the four Phase 3 trials is over one-third enrolled, and
initial data from the Phase 3 program is expected in 2010. In addition, a Phase
2 study of aflibercept in 1st line
metastatic colorectal cancer in combination with folinic acid (leucovorin),
5-fluorouracil, and oxaliplatin (the AFFIRM study) began recruiting patients in
January 2009.
Aflibercept is also being studied in a Phase 2 single-agent study in advanced ovarian cancer (AOC) patients with symptomatic malignant ascites (SMA). This trial is now fully enrolled and we expect to have initial data from this trial by mid 2009.
VEGF Trap-Eye – Ophthalmologic
Diseases
VEGF Trap-Eye is a specially
purified and formulated form of VEGF Trap for use in intraocular applications.
Regeneron and collaborator Bayer HealthCare are testing VEGF Trap-Eye in a Phase
3 program in patients with the neovascular form of age-related macular
degeneration (wet AMD). Regeneron and Bayer HealthCare also initiated a Phase 2
study of VEGF Trap-Eye in patients with diabetic macular edema (DME) in late
2008.
The Phase 3 trials in wet AMD, known as VIEW 1 and VIEW 2 (VEGF Trap: Investigation of Efficacy and Safety in Wet age-related macular degeneration), are comparing VEGF Trap-Eye and ranibizumab (Lucentis®, a registered trademark of Genentech, Inc.), an anti-angiogenic agent approved for use in wet AMD. VIEW 1 is being conducted in North America and VIEW 2 is being conducted in Europe, Asia Pacific, Japan, and Latin America. The VIEW 1 and VIEW 2 trials are both evaluating dosing intervals of four and eight weeks for VEGF Trap-Eye compared with ranibizumab dosed according to its U.S. label every four weeks over the first year. As needed dosing (PRN) with both agents will be evaluated in the second year of the studies. The VIEW 1 and VIEW 2 trials are expected to complete enrollment in 2009, and initial data are expected in late 2010.
The recently initiated Phase 2 DME study, known as the DA VINCI study, is a double-masked, randomized, controlled trial that is evaluating four different VEGF Trap-Eye regimens versus laser treatment. The study will be enrolling approximately 200 patients in the U.S., Canada, European Union, and Australia. The patients in the study will be treated for 52 weeks followed up by six additional months of safety evaluation. The primary efficacy endpoint is the change in best corrected visual acuity (BCVA) from baseline to week 24.
Monoclonal
Antibodies
Regeneron and sanofi-aventis
are collaborating on the discovery, development, and commercialization of fully
human monoclonal antibodies generated by Regeneron using its VelocImmune® technology. The first therapeutic antibodies to enter clinical
development under the collaboration are REGN88, an antibody to the interleukin-6
receptor (IL-6R) that is being evaluated in rheumatoid arthritis, and REGN475,
an antibody to Nerve Growth Factor (NGF) that is being developed for the
treatment of pain. In addition, a Phase 1 trial is in the process of being
initiated for REGN421, an antibody to Delta-like ligand-4 (Dll4) that will be
evaluated in oncology in patients with advanced malignancies. Over the course of
the next several years, the Company and sanofi-aventis plan to advance an
average of two to three new fully human antibodies into clinical development
each year.
Financial Results
Revenues
Total revenues decreased to $55.8 million in the fourth quarter of 2008
from $64.7 million in the same quarter of 2007 and increased to $238.5 million
for the full year 2008 from $125.0 million for the same period of 2007. The
Company’s revenue was comprised of contract research and development revenue,
technology licensing revenue, and net product sales.
Contract Research and Development
Revenue
Contract research and development
revenue relates primarily to the Company’s aflibercept and antibody
collaborations with sanofi-aventis and the Company’s VEGF Trap-Eye collaboration
with Bayer HealthCare. Contract research and development revenue for the three
months and years ended December 31, 2008 and 2007, consisted of the
following:
| Three months ended | Year ended | |||||||||||
| December 31, | December 31, | |||||||||||
| (In millions) | 2008 | 2007 | 2008 | 2007 | ||||||||
| Contract research & development revenue | ||||||||||||
| Sanofi-aventis | $ | 37.6 | $ | 17.2 | $ | 154.0 | $ | 51.7 | ||||
| Bayer HealthCare | 3.0 | 35.9 | 31.2 | 35.9 | ||||||||
| Other | 1.7 | 1.6 | 7.0 | 9.0 | ||||||||
| Total contract research & development revenue | $ | 42.3 | $ | 54.7 | $ | 192.2 | $ | 96.6 | ||||
For the three months and years ended December 31, 2008 and 2007, contract research and development revenue from sanofi-aventis consisted of the following:
| Three months ended | Year ended | |||||||||||
| December 31, | December 31, | |||||||||||
| (In millions) | 2008 | 2007 | 2008 | 2007 | ||||||||
| Aflibercept: | ||||||||||||
| Regeneron expense reimbursement | $ | 6.3 | $ | 10.5 | $ | 35.6 | $ | 38.3 | ||||
| Recognition of deferred revenue related to up-front payments | 2.5 | 2.1 | 8.8 | 8.8 | ||||||||
| Total aflibercept | 8.8 | 12.6 | 44.4 | 47.1 | ||||||||
| Antibody: | ||||||||||||
| Regeneron expense reimbursement | 25.5 | 3.7 | 97.9 | 3.7 | ||||||||
| Recognition of deferred revenue related to up-front payment | 2.6 | 0.9 | 10.5 | 0.9 | ||||||||
| Other | 0.7 | 1.2 | ||||||||||
| Total antibody | 28.8 | 4.6 | 109.6 | 4.6 | ||||||||
| Total sanofi-aventis contract research & development revenue | $ | 37.6 | $ | 17.2 | $ | 154.0 | $ | 51.7 | ||||
Sanofi-aventis’ reimbursement of Regeneron’s aflibercept expenses decreased for the three months and year ended December 31, 2008, compared to the same periods in 2007, primarily due to lower costs related to manufacturing aflibercept clinical supplies.
Revenue under the antibody collaboration increased for the three months and year ended December 31, 2008 compared to the same periods in 2007 due to the initiation of the collaboration in November 2007.
For the three months and years ended December 31, 2008 and 2007, contract research and development revenue from Bayer HealthCare consisted of the following:
| Three months ended | Year ended | |||||||||||
| December 31, | December 31, | |||||||||||
| (In millions) | 2008 | 2007 | 2008 | 2007 | ||||||||
| Cost-sharing of Regeneron VEGF Trap-Eye development | ||||||||||||
| expenses | $ | 0.5 | $ | 20.0 | $ | 18.8 | $ | 20.0 | ||||
| Recognition of deferred revenue related to up-front and | ||||||||||||
| milestone payments | 2.5 | 15.9 | 12.4 | 15.9 | ||||||||
| Total Bayer HealthCare contract research & development | ||||||||||||
| revenue | $ | 3.0 | $ | 35.9 | $ | 31.2 | $ | 35.9 | ||||
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 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 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 is 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. 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.
Under the terms of the Bayer HealthCare collaboration, in 2008, the first $70.0 million of agreed-upon VEGF Trap-Eye development expenses incurred by the Company and Bayer HealthCare under a global development plan were shared equally, and the Company was solely responsible for up to the next $30.0 million. During the fourth quarter of 2008, Regeneron was solely responsible for most of the collaboration’s VEGF Trap-Eye development expenses. As a result, in the fourth quarter of 2008, the portion of the Company’s VEGF Trap-Eye development expenses that were reimbursable from Bayer HealthCare, and recognized as contract research and development revenue, amounted to only $0.5 million.
Technology Licensing
Revenue
Regeneron has entered into
non-exclusive license agreements with AstraZeneca and Astellas that allow those
companies to utilize VelocImmune® technology in their internal
research programs to discover human monoclonal antibodies. Each company made
$20.0 million annual, non-refundable payments in each of 2007 and 2008 and
agreed to make up to four additional annual payments of $20.0 million, subject
to the ability to terminate their agreements after making two such additional
payments. Upon receipt, these payments are deferred and are recognized as
revenue ratably over approximately the ensuing year of each agreement. Regeneron
will also receive a mid-single-digit royalty on sales of any antibodies
discovered utilizing VelocImmune.
Net Product Sales
The Company shipped $10.7 million of ARCALYST®
(rilonacept) to its distributors in 2008 and recorded $3.5 million and $6.3
million in product sales revenue for the three months and year ended December
31, 2008. Revenue and deferred revenue from product sales are recorded net of
applicable provisions for prompt pay discounts, product returns, estimated
rebates payable under governmental programs (including Medicaid), distributor
fees, and other sales-related costs. At December 31, 2008, $4.0 million of
ARCALYST net product sales was included in deferred revenue in the Company’s
financial statements.
Expenses
Total operating expenses for the
fourth quarter of 2008 were $90.4 million, 19 percent higher than the same
period in 2007, and $328.3 million for the full year 2008, 37 percent higher
than for the same period of 2007. Average headcount increased to 903 for the
fourth quarter of 2008 compared to 665 for the same period in 2007 and increased
to 810 for the full year 2008 from 627 for the full year 2007, due primarily to
the Company’s expanding research and development activities principally in
connection with the Company’s antibody collaboration with sanofi-aventis.
Operating expenses included non-cash compensation expense related to employee stock option and restricted stock awards of $7.8 million in the fourth quarter of 2008 and $32.5 million for the full year of 2008, compared with $7.5 million and $28.1 million, respectively, for the same periods of 2007.
Research and development (R&D) expenses increased to $76.3 million in the fourth quarter of 2008 from $64.8 million in the comparable quarter of 2007, and to $278.0 million for the full year 2008 from $201.6 million for the same period of 2007. In the fourth quarter and for the full year of 2008, the Company incurred higher R&D costs primarily related to additional R&D headcount, clinical development costs for ARCALYST and REGN88, research and preclinical development costs associated with our antibody programs, and facility-related costs to support the Company’s expanded R&D activities. In addition, for the full year of 2008, the Company incurred higher R&D costs related to clinical development of VEGF Trap-Eye and manufacturing supplies of our drug product candidates, especially our monoclonal antibodies. Also, as described above, commencing in the fourth quarter of 2007, the Company began recognizing as additional R&D expense, the portion of Bayer HealthCare’s VEGF Trap-Eye development expenses that the Company is obligated to reimburse.
Selling, general, and administrative (SG&A) expenses increased to $13.5 million in the fourth quarter of 2008 from $11.4 million in the comparable quarter of 2007, and to $49.4 million for the full year 2008 from $37.9 million for the full year 2007. In 2008, the Company incurred $5.2 million of selling expenses related to ARCALYST® (rilonacept) for the treatment of CAPS. In addition, the Company incurred higher compensation expense and recruitment costs associated with expanding the Company’s SG&A headcount, higher professional fees related to various general corporate matters, and higher SG&A facility related costs.
Other Income and
Expense
Investment income increased to
$2.6 million in the fourth quarter of 2008 from $1.5 million in the comparable
quarter of 2007, and decreased to $18.2 million for the full year 2008 from
$20.9 million for the full year 2007. For the full year 2008, investment income
decreased primarily due to lower yields on our cash and marketable securities.
The Company recognized charges of $0.2 million and $5.1 million for the fourth
quarters of 2008 and 2007, respectively, and $2.5 million and $5.9 million for
the full year 2008 and 2007, respectively, related to certain marketable
securities that were determined to be other-than-temporarily impaired. For the
full year 2008, these charges were partially offset by realized gains of $1.2
million on sales of marketable securities during the year.
During the second and third quarters of 2008, the Company repurchased $82.5 million in principal amount of its 5.5 percent Convertible Senior Subordinated Notes. In connection with the repurchased notes, the Company recognized a $0.9 million loss on early extinguishment of debt. The remaining $117.5 million of these notes were repaid in full upon their maturity in October 2008.
Income Tax Expense
In the fourth quarter of
2008, the Company recognized a $0.7 million income tax benefit, resulting from a
provision in the Housing Assistance Tax Act of 2008 that allowed the Company to
claim a refund for certain unused pre-2006 research tax credits. For the full
year 2008, income tax expense was $2.4 million and consisted primarily of
alternative minimum tax, which resulted from the utilization of certain net
operating loss carry-forwards, that would otherwise have expired over the next
several years, to offset income for tax purposes.
About Regeneron
Pharmaceuticals
Regeneron is a fully
integrated biopharmaceutical company that discovers, develops, and
commercializes medicines for the treatment of serious medical conditions. In
addition to ARCALYST® (rilonacept) Injection for Subcutaneous Use,
its first commercialized product, Regeneron has therapeutic candidates in
clinical trials for the potential treatment of cancer, eye diseases,
inflammatory diseases, and pain, and has preclinical programs in other diseases
and disorders. Additional information about Regeneron and recent news releases
are available on Regeneron’s web site at www.regeneron.com.
This news release discusses historical information and includes forward-looking statements about Regeneron and its products, development programs, finances, and business, all of which involve a number of risks and uncertainties, such as risks associated with preclinical and clinical development of Regeneron’s drug candidates, determinations by regulatory and administrative governmental authorities which may delay or restrict Regeneron’s ability to continue to develop or commercialize its product and drug candidates, competing drugs that are superior to Regeneron’s product and drug candidates, uncertainty of market acceptance of Regeneron’s product and drug candidates, unanticipated expenses, the availability and cost of capital, the costs of developing, producing, and selling products, the potential for any collaboration agreement, including Regeneron’s 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, 2008. 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.
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Contacts Information: |
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|
Peter Dworkin |
Laura Lindsay | |
|
Kelly Hershkowitz |
REGENERON PHARMACEUTICALS,
INC.
CONDENSED BALANCE SHEETS (Unaudited)
(In thousands)
| December 31, | December 31, | |||||
| 2008 | 2007 | |||||
| ASSETS | ||||||
| Cash, restricted cash, and marketable securities | $ | 527,461 | $ | 846,279 | ||
| Receivables | 35,212 | 18,320 | ||||
| Property, plant, and equipment, net | 87,853 | 58,304 | ||||
| Other assets | 19,512 | 13,355 | ||||
| Total assets | $ | 670,038 | $ | 936,258 | ||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||
| Accounts payable, accrued expenses, and other liabilities | $ | 41,261 | $ | 39,232 | ||
| Deferred revenue | 209,925 | 236,759 | ||||
| Notes payable | 200,000 | |||||
| Stockholders' equity | 418,852 | 460,267 | ||||
| Total liabilities and stockholders' equity | $ | 670,038 | $ | 936,258 | ||
REGENERON PHARMACEUTICALS,
INC.
CONDENSED STATEMENTS OF OPERATIONS
(Unaudited)
(In thousands, except
per share data)
| For the three months | For the year | |||||||||||||||
| ended December 31, | ended December 31, | |||||||||||||||
| 2008 | 2007 | 2008 | 2007 | |||||||||||||
| Revenues | ||||||||||||||||
| Contract research and development | $ | 42,294 | $ | 54,730 | $ | 192,208 | $ | 96,603 | ||||||||
| Technology licensing | 10,000 | 10,000 | 40,000 | 28,421 | ||||||||||||
| Net product sales | 3,543 | 6,249 | ||||||||||||||
| 55,837 | 64,730 | 238,457 | 125,024 | |||||||||||||
| Expenses | ||||||||||||||||
| Research and development | 76,314 | 64,825 | 278,016 | 201,613 | ||||||||||||
| Selling, general, and administrative | 13,491 | 11,439 | 49,348 | 37,865 | ||||||||||||
| Cost of goods sold | 631 | 923 | ||||||||||||||
| 90,436 | 76,264 | 328,287 | 239,478 | |||||||||||||
| Loss from operations | (34,599 | ) | (11,534 | ) | (89,830 | ) | (114,454 | ) | ||||||||
| Other income (expense) | ||||||||||||||||
| Investment income | 2,648 | 1,473 | 18,161 | 20,897 | ||||||||||||
| Interest expense | (295 | ) | (3,010 | ) | (7,752 | ) | (12,043 | ) | ||||||||
| Loss on early extinguishment of debt | (938 | ) | ||||||||||||||
| 2,353 | (1,537 | ) | 9,471 | 8,854 | ||||||||||||
| Net loss before income tax expense | (32,246 | ) | (13,071 | ) | (80,359 | ) | (105,600 | ) | ||||||||
| Income tax expense (benefit) | (728 | ) | 2,351 | |||||||||||||
| Net loss | $ | (31,518 | ) | $ | (13,071 | ) | $ | (82,710 | ) | $ | (105,600 | ) | ||||
| Net loss per share amounts, basic and diluted | $ | (0.40 | ) | $ | (0.19 | ) | $ | (1.05 | ) | $ | (1.59 | ) | ||||
| Weighted average shares outstanding, basic and diluted | 79,190 | 67,754 | 78,827 | 66,334 | ||||||||||||