Cubist Pharmaceuticals, Inc. CBST today announced results for the second quarter ended June 30, 2014. The Company will host a conference call and webcast today at 5:00 p.m. ET (details below).
Financial highlights for the second quarter of 2014 (unaudited)
- Q2 2014 total net revenues were $294.4 million, up 14% compared to $258.8 million in Q2 2013.
- U.S. CUBICIN® (daptomycin for injection) net product revenues increased 3% to $234.7 million from $227.1 million in Q2 2013 which included a $6.6 million favorable adjustment to revenue reserves.
- International product revenues were $17.5 million compared to $15.0 million in Q2 2013.
- Non-GAAP adjusted operating income was $41.4 million compared to $51.3 million in the second quarter of 2013. GAAP operating income was $42.2 million compared to $28.1 million in the second quarter of 2013.
- Non-GAAP diluted earnings per share (EPS) was $0.23 compared to $0.42 in the second quarter of 2013. GAAP diluted EPS was $0.30 compared to $0.23 in the second quarter of 2013.
“This was another exciting quarter for Cubist in which we launched an important new antibiotic treatment and made significant progress advancing another key pipeline program,” said Michael Bonney, CEO of Cubist. “The FDA's approval of SIVEXTRO™, and acceptance of our New Drug Application for our potential blockbuster, ceftolozane/tazobactam, reinforces our position as the worldwide leader in the research, development, and commercialization of antibiotics with activity against a range of resistant and problematic pathogens.”
As of June 30, 2014, Cubist had $643.5 million in cash, cash equivalents and investments. The total number of Cubist's common shares outstanding as of June 30, 2014, was 75,570,915.
Recent Pipeline Highlights
- On June 20, Cubist received U.S. Food and Drug Administration (FDA) approval for and subsequently launched SIVEXTRO™ (tedizolid phosphate). SIVEXTRO is indicated for the treatment of adult acute bacterial skin and skin structure infections caused by susceptible Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), which has been categorized by the U.S. Centers for Disease Control and Prevention (CDC) as a serious public health threat.
- On June 19, the FDA accepted Cubist's New Drug Application (NDA) for its investigational antibiotic ceftolozane/tazobactam with Priority Review. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) action date of December 21, 2014. Cubist is seeking FDA approval of ceftolozane/tazobactam for the treatment of complicated urinary tract Infections (cUTI) and complicated intra-abdominal infections (cIAI).
- On May 9, Cubist announced the first detailed results from positive pivotal Phase 3 clinical trials of ceftolozane/tazobactam in development to treat serious infections including cUTI and cIAI. Cubist presented data on microbiological eradication of key problematic Gram-negative pathogens, including Pseudomonas aeruginosa and extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli (E. coli) and Klebsiella pneumoniae.
Use of Non-GAAP Financial Measures
Cubist has presented certain non-GAAP financial measures, including non-GAAP adjusted operating income, non-GAAP net income, non-GAAP diluted earnings per share, non-GAAP cost of product revenues, non-GAAP R&D expenses, non-GAAP SG&A expenses, non-GAAP other income (expense) and non-GAAP provision for income taxes. These non-GAAP financial measures exclude certain amounts, expenses or income, from the corresponding financial measures determined in accordance with accounting principles generally accepted in the U.S. (GAAP). Management believes this non-GAAP information is useful for investors, taken in conjunction with Cubist's GAAP financial statements, because it provides greater transparency regarding Cubist's operating performance. Management uses these measures, among other factors, to assess and analyze operational results and trends and to make financial and operational decisions. Non-GAAP information is not prepared under a comprehensive set of accounting rules and should only be used to supplement an understanding of Cubist's operating results as reported under GAAP, not as a substitute for GAAP. In addition, these non-GAAP financial measures are unlikely to be comparable with non-GAAP information provided by other companies. The determination of the amounts that are excluded from non-GAAP financial measures is a matter of management judgment and depends upon, among other factors, the nature of the underlying expense or income amounts. Reconciliations between these non-GAAP financial measures and the most comparable GAAP financial measures are included in the tables accompanying this press release after the unaudited condensed consolidated financial statements.
***********************CONFERENCE CALL & WEBCAST INFORMATION***********************
CUBIST Q2 2014 FINANCIAL RESULTS
Tuesday, July 22, 2014 at 5:00 pm
ET
U.S./Canada Attendee Dial-in: (855) 319-7654
International Attendee
Dial-in: (484) 756-4327
Conference ID: 55596186
24-HOUR REPLAY U.S./CANADA: (855) 859-2056
24-HOUR REPLAY
INTERNATIONAL: (404) 537-3406
Conference ID: 55596186
CALL WILL ALSO BE BROADCAST LIVE, LISTEN ONLY, VIA THE WEB AT:
https://cubist.webex.com/cubist/onstage/g.php?t=a&d=625014646
Attendee
Password: 07222014
Replay will be available for 90 days at www.cubist.com
*********************************************************************************
About Cubist
Cubist Pharmaceuticals, Inc. is a global biopharmaceutical company focused on the research, development, and commercialization of pharmaceutical products that address significant unmet medical needs in the acute care environment. Cubist is headquartered in Lexington, Massachusetts, with a central international office located in Zurich, Switzerland. Additional information can be found at Cubist's web site at www.cubist.com. Also, connect with Cubist on Twitter @cubistbiopharma and @cubistcareers, LinkedIn, or YouTube.
Cubist Safe Harbor Statement
This press release contains forward-looking statements. Any statements contained herein which do not describe historical facts, including but not limited to, statements regarding: our expected second quarter 2014 financial results; our belief that ceftolozane/tazobactam has the potential to achieve blockbuster status; the anticipated PDUFA action date for our NDA for ceftolozane/tazobactam; and the therapeutic potential of SIVEXTRO and ceftolozane/tazobactam, are forward-looking statements which involve risks and uncertainties that could cause actual results to differ materially from those discussed in such forward-looking statements. Such risks and uncertainties include, among others: the risk that our final second quarter 2014 financial results will differ materially from our expected results disclosed in this release; regulatory developments, including the risk that the FDA may not agree with our interpretation of the results from the clinical studies of ceftolozane/tazobactam, may not approve on a timely basis or at all our NDA for ceftolozane/tazobactam or may require additional data, analysis, information or further studies that may not be clinically feasible or financially practicable; the review of our NDA for ceftolozane/tazobactam may take longer than anticipated, including as a result of internal FDA constraints; our ability to achieve our strategic milestones and initiatives, including as a result of our ability to continue to grow revenues from the sale of our commercial products, generic and other competition, manufacturing issues, our ability to successfully develop, gain marketing approval for and commercially launch our product candidates for their planned indications and on their expected timelines, and our ability to discover, in-license or acquire new products and product candidates; any marketing approval for ceftolozane/tazobactam may impose significant limitations on its use and additional post-marketing requirements; our ability to obtain adequate pricing and reimbursement levels for our products; our ability to successfully commercialize our products; the acceptance of and demand for new pharmaceutical products; competitive risks from current and future therapeutic alternatives to our products; our ability to obtain, maintain and enforce intellectual property for our products and product candidates; additional clinical trials of SIVEXTRO and/or ceftolozane/tazobactam may produce negative or inconclusive results or may not be initiated or conducted in a timely manner; technical difficulties, excessive costs or other issues relating to the manufacture or supply of our products and product candidates, including our ability to work with our third party contract manufacturers that manufacture and supply our product and product candidates on our behalf; our ability to work with, and the performance of our third party contract research organizations that help us conduct our clinical trials; we may encounter other unanticipated or unexpected risks with respect to the development or manufacture of our products and product candidates; the fact that drug discovery and development is complex, time consuming, expensive and fraught with a high risk of failure; and those additional factors discussed in our most recent Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q filed with the Securities and Exchange Commission. We caution investors not to place considerable reliance on the forward-looking statements contained in this press release. These forward-looking statements speak only as of the date of this document, and we undertake no obligation to update or revise any of these statements.
Tables to follow
CUBIST PHARMACEUTICALS, INC. CONDENSED CONSOLIDATED BALANCE SHEETS UNAUDITED (in thousands) |
||||||||
June 30, 2014 | December 31, 2013 | |||||||
ASSETS | ||||||||
Cash, cash equivalents and investments | $ | 643,482 | $ | 578,558 | ||||
Accounts receivable, net | 107,395 | 123,155 | ||||||
Inventory | 113,774 | 116,829 | ||||||
Property and equipment, net | 179,584 | 177,544 | ||||||
Deferred tax assets, net | 65,556 | 52,108 | ||||||
In-process research and development | 237,400 | 896,400 | ||||||
Goodwill | 383,018 | 383,018 | ||||||
Other intangible assets, net | 1,350,383 | 721,066 | ||||||
Other assets | 100,380 | 97,143 | ||||||
Total assets | $ | 3,180,972 | $ | 3,145,821 | ||||
LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||||
Accounts payable and accrued liabilities | $ | 256,757 | $ | 276,955 | ||||
Deferred tax liabilities, net | 363,358 | 357,802 | ||||||
Deferred revenue | 34,335 | 37,421 | ||||||
Contingent consideration | 165,230 | 223,322 | ||||||
Debt and other liabilities, net | 873,593 | 856,590 | ||||||
Total liabilities | 1,693,273 | 1,752,090 | ||||||
Total stockholders' equity | 1,487,699 | 1,393,731 | ||||||
Total liabilities and stockholders' equity | $ | 3,180,972 | $ | 3,145,821 |
CUBIST PHARMACEUTICALS, INC. CONDENSED CONSOLIDATED STATEMENTS OF INCOME UNAUDITED (in thousands, except share and per share data) |
||||||||||||||||
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
2014 | 2013 | 2014 | 2013 | |||||||||||||
Revenues: | ||||||||||||||||
U.S. CUBICIN product revenues, net | $ | 234,723 | $ | 227,117 | $ | 446,907 | $ | 429,162 | ||||||||
U.S. DIFICID product revenues, net | 15,930 | — | 30,283 | — | ||||||||||||
U.S. ENTEREG product revenues, net | 14,606 | 12,386 | 28,527 | 23,589 | ||||||||||||
Total U.S. product revenues, net | 265,259 | 239,503 | 505,717 | 452,751 | ||||||||||||
International product revenues | 17,485 | 14,959 | 34,512 | 27,362 | ||||||||||||
Other revenues | 11,654 | 4,317 | 15,402 | 8,595 | ||||||||||||
Total revenues, net | 294,398 | 258,779 | 555,631 | 488,708 | ||||||||||||
Costs and expenses: | ||||||||||||||||
Cost of product revenues | 88,613 | 63,041 | 162,154 | 118,716 | ||||||||||||
Research and development expense | 104,862 | 115,190 | 225,465 | 229,399 | ||||||||||||
Contingent consideration (income) expense | (24,774 | ) | 2,586 | (58,092 | ) | 4,639 | ||||||||||
Selling, general and administrative expense | 80,057 | 49,889 | 149,719 | 98,090 | ||||||||||||
Restructuring charges | 3,469 | — | 5,908 | — | ||||||||||||
Total costs and expenses | 252,227 | 230,706 | 485,154 | 450,844 | ||||||||||||
Operating income | 42,171 | 28,073 | 70,477 | 37,864 | ||||||||||||
Total other expense (income), net | 14,135 | 6,678 | 28,222 | 12,880 | ||||||||||||
Income before income taxes | 28,036 | 21,395 | 42,255 | 24,984 | ||||||||||||
Provision (benefit) for income taxes | 4,008 | 6,153 | (6,006 | ) | 3,654 | |||||||||||
Net income | $ | 24,028 | $ | 15,242 | $ | 48,261 | $ | 21,330 | ||||||||
Basic net income per common share | $ | 0.32 | $ | 0.23 | $ | 0.64 | $ | 0.33 | ||||||||
Diluted net income per common share | $ | 0.30 | $ | 0.23 | $ | 0.61 | $ | 0.32 | ||||||||
Shares used in calculating: | ||||||||||||||||
Basic net income per common share | 75,421,354 | 65,558,376 | 75,179,275 | 65,248,707 | ||||||||||||
Diluted net income per common share | 86,108,783 | 67,731,976 | 85,853,847 | 67,385,141 |
CUBIST PHARMACEUTICALS, INC. RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION UNAUDITED (in thousands) |
||||||||||||||||
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
2014 | 2013 | 2014 | 2013 | |||||||||||||
Operating income reconciliation: 1 | ||||||||||||||||
GAAP operating income | $ | 42,171 | $ | 28,073 | $ | 70,477 | $ | 37,864 | ||||||||
Cost of product revenues adjustments 1 | 17,157 | 5,611 | 33,141 | 10,999 | ||||||||||||
Research and development expense adjustments 1 | 1,833 | 15,000 | 6,555 | 40,000 | ||||||||||||
Contingent consideration (income) expense | (24,774 | ) | 2,586 | (58,092 | ) | 4,639 | ||||||||||
Selling, general and administrative expense adjustments 1 | 1,497 | — | 2,158 | — | ||||||||||||
Restructuring charges | 3,469 | — | 5,908 | — | ||||||||||||
Non-GAAP adjusted operating income | $ | 41,353 | $ | 51,270 | $ | 60,147 | $ | 93,502 | ||||||||
Non-GAAP other expense (income) 2 | 5,577 | 3,008 | 11,241 | 5,603 | ||||||||||||
Non-GAAP provision for income taxes 2 | 16,732 | 15,240 | 22,061 | 28,705 | ||||||||||||
Non-GAAP net income | $ | 19,044 | $ | 33,022 | $ | 26,845 | $ | 59,194 | ||||||||
|
1 Detail on the adjustments included herein is provided in the tables below.
2 A reconciliation to the most comparable GAAP financial measure is included in the tables below.
CUBIST PHARMACEUTICALS, INC. RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION UNAUDITED (in thousands, except percentages) |
|||||||||||||||||
Three Months Ended June 30, | Six Months Ended June 30, | ||||||||||||||||
2014 | 2013 | 2014 | 2013 | ||||||||||||||
Cost of product revenues reconciliation: | |||||||||||||||||
GAAP cost of product revenues | $ | 88,613 | $ | 63,041 | $ | 162,154 | $ | 118,716 | |||||||||
Intangible asset amortization | (16,052 | ) | (4,552 | ) | (30,790 | ) | (8,977 | ) | |||||||||
Inventory fair value step-up | (1,105 | ) | (1,059 | ) | (2,351 | ) | (2,022 | ) | |||||||||
Non-GAAP cost of product revenues | $ | 71,456 | $ | 57,430 | $ | 129,013 | $ | 107,717 | |||||||||
Product gross margin reconciliation: | |||||||||||||||||
GAAP product gross margin | 68.7 | % | 75.2 | % | 70.0 | % | 75.3 | % | |||||||||
Intangible asset amortization | 5.7 | % | 1.8 | % | 5.7 | % | 1.9 | % | |||||||||
Inventory fair value step-up | 0.4 | % | 0.4 | % | 0.4 | % | 0.4 | % | |||||||||
Non-GAAP product gross margin | 74.8 | % | 77.4 | % | 76.1 | % | 77.6 | % | |||||||||
Research and development expenses reconciliation: | |||||||||||||||||
GAAP research and development expenses | $ | 104,862 | $ | 115,190 | $ | 225,465 | $ | 229,399 | |||||||||
Acquisition-related expenses | (1,017 | ) | — | (4,922 | ) | — | |||||||||||
Intangible asset amortization | (816 | ) | — | (1,633 | ) | — | |||||||||||
Upfront license fees | — | (15,000 | ) | — | (40,000 | ) | |||||||||||
Non-GAAP research and development expenses | $ | 103,029 | $ | 100,190 | $ | 218,910 | $ | 189,399 | |||||||||
Selling, general and administrative expenses reconciliation: | |||||||||||||||||
GAAP selling, general and administrative expenses | $ | 80,057 | $ | 49,889 | $ | 149,719 | $ | 98,090 | |||||||||
Acquisition-related expenses | (1,497 | ) | — | (2,158 | ) | — | |||||||||||
Non-GAAP selling, general and administrative expenses | $ | 78,560 | $ | 49,889 | $ | 147,561 | $ | 98,090 | |||||||||
Other (income) expense reconciliation: | |||||||||||||||||
GAAP other (income) expense | $ | 14,135 | $ | 6,678 | $ | 28,222 | $ | 12,880 | |||||||||
Non-cash debt discount amortization | (8,558 | ) | (3,670 | ) | (16,981 | ) | (7,277 | ) | |||||||||
Non-GAAP other (income) expense | $ | 5,577 | $ | 3,008 | $ | 11,241 | $ | 5,603 | |||||||||
Provision (benefit) for income taxes reconciliation: | |||||||||||||||||
GAAP provision (benefit) for income taxes | $ | 4,008 | $ | 6,153 | $ | (6,006 | ) | $ | 3,654 | ||||||||
Tax adjustment | 12,724 | 9,087 | 28,067 | 25,051 | |||||||||||||
Non-GAAP provision for income taxes | $ | 16,732 | $ | 15,240 | $ | 22,061 | $ | 28,705 |
CUBIST PHARMACEUTICALS, INC. RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION UNAUDITED (in thousands, except share and per share amounts) |
||||||||||||||||||||
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||||||
2014 | 2013 | 2014 | 2013 | |||||||||||||||||
Non-GAAP net income reconciliation: |
||||||||||||||||||||
GAAP net income | $ | 24,028 | $ | 15,242 | $ | 48,261 | $ | 21,330 | ||||||||||||
Non-cash debt discount amortization | 8,558 | 3,670 | 16,981 | 7,277 | ||||||||||||||||
Intangible asset amortization | 16,868 | 4,552 | 32,423 | 8,977 | ||||||||||||||||
Inventory fair value step-up | 1,105 | 1,059 | 2,351 | 2,022 | ||||||||||||||||
Restructuring charges | 3,469 | — | 5,908 | — | ||||||||||||||||
Acquisition-related expenses | 2,514 | — | 7,080 | — | ||||||||||||||||
Upfront license fees | — | 15,000 | — | 40,000 | ||||||||||||||||
Contingent consideration (income) expense | (24,774 | ) | 2,586 | (58,092 | ) | 4,639 | ||||||||||||||
Tax adjustment | (12,724 | ) | (9,087 | ) | (28,067 | ) | (25,051 | ) | ||||||||||||
Non-GAAP net income | $ | 19,044 | $ | 33,022 | $ | 26,845 | $ | 59,194 | ||||||||||||
Diluted earnings per common share reconciliation: |
||||||||||||||||||||
GAAP diluted earnings per common share | $ | 0.30 | $ | 0.23 | $ | 0.61 | $ | 0.32 | ||||||||||||
Non-GAAP dilutive adjustments | (0.07 | ) | (1 | ) | 0.19 | (1 | ) | (0.27 | ) | (1 | ) | 0.45 | (1 | ) | ||||||
Non-GAAP diluted earnings per common share | $ | 0.23 | $ | 0.42 | $ | 0.34 | $ | 0.77 | ||||||||||||
Shares used in diluted per common share calculation reconciliation: |
||||||||||||||||||||
GAAP shares used in diluted earnings per common share | 86,108,783 | 67,731,976 | 85,853,847 | 67,385,141 | ||||||||||||||||
Non-GAAP dilutive share adjustments | 4,246,131 | (2 | ) | 15,424,084 | (2 | ) | — | 15,424,118 | (2 | ) | ||||||||||
Non-GAAP shares used in diluted earnings per common share | 90,354,914 | 83,156,060 | 85,853,847 | 82,809,259 | ||||||||||||||||
|
1. Includes impact of non-GAAP adjustments from GAAP net income to non-GAAP net income and add back of interest expense and debt issuance costs on Cubist's outstanding convertible notes, net of tax effect
2. Additional dilutive weighted average shares issuable upon conversion of Cubist's outstanding convertible notes
Cubist Pharmaceuticals, Inc.
INVESTORS:
Eileen C. McIntyre,
781-860-8533
Vice President, Investor Relations
eileen.mcintyre@cubist.com
or
MEDIA:
Julie
DiCarlo, 781-860-8063
Senior Director, Corporate Communications
julie.dicarlo@cubist.com
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