Revenue for the third quarter of 2017 was $4.3M.
Inflection Points for Key Development Programs Anticipated Throughout 2018
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| [07-November-2017] |
| DUBLIN, Nov. 7, 2017 /PRNewswire/ -- Theravance Biopharma today reported financial results for the third quarter ended September 30, 2017. Revenue for the third quarter of 2017 was $4.3 million. The third quarter operating loss was $57.0 million, or $46.3 million excluding non-cash share-based compensation expense of $10.7 million. Cash, cash equivalents, and marketable securities totaled $434.4 million as of September 30, 2017. Rick E Winningham, Chairman and Chief Executive Officer, commented: “In 2017, we continue to demonstrate the potential of our portfolio with encouraging clinical data across multiple key programs. Looking forward, we are positioned to achieve numerous clinical and regulatory milestones, with a plan to deliver on the promise of developing differentiated medicines for patients in need.” Recent Updates1
Expected Upcoming Milestones and Events
Notes: Third Quarter Financial Results Revenue Revenue for the third quarter of 2017 was $4.3 million, primarily related to US net product sales of VIBATIV® of $4.1 million. In the same period in 2016, net product sales of VIBATIV® were $3.9 million and revenue from collaborative arrangements was $15.2 million, primarily driven by non-recurring revenue of $15.1 million associated with the Takeda collaboration. Research and Development (R&D) Expenses R&D expenses for the third quarter of 2017 were $39.3 million representing an increase of $7.4 million compared to the same period in 2016. The increase is driven by costs associated with the progression of our key programs as well as employee-related costs. Third quarter R&D expenses include non-cash share-based compensation expense of $5.0 million. Selling, General and Administrative (SG&A) Expenses SG&A expenses for the third quarter of 2017 were $20.9 million, representing an increase of $0.7 million compared to the same period in 2016. The increase is primarily due to employee-related costs and share-based compensation, partially offset by a reduction in external expenses related to commercialization activities. Third quarter SG&A expenses include non-cash share-based compensation expense of $5.7 million. Other-than-Temporary Impairment Loss In the third quarter, a non-cash impairment charge of $8.0 million was recorded to write off the full carrying value of the non-marketable equity securities of Trek Therapeutics, PBC (TREKtx). These securities were received in 2015, pursuant to a license agreement granting TREKtx rights to TD-6450, an internally discovered NS5A inhibitor. Cash, Cash Equivalents and Marketable Securities Cash, cash equivalents and marketable securities, excluding restricted cash, totaled $434.4 million as of September 30, 2017. 2017 Financial Guidance The Company’s guidance on operating loss excluding non-cash share-based compensation for the full-year of 2017 remains unchanged at $205.0 million to $215.0 million. The actual amount could be above or below this forecast as a result of a variety of factors impacting our business, including the timing and cost of clinical and non-clinical studies associated with our key programs and net product sales of VIBATIV®. Conference Call Today at 5:00 pm ET Theravance Biopharma will hold a conference call today at 5:00 pm ET. To participate in the live call by telephone, please dial (855) 296-9648 from the US, or (920) 663-6266 for international callers, using the confirmation code 96855845. Those interested in listening to the conference call live via the internet may do so by visiting Theravance Biopharma’s website at www.theravance.com, under the Investor Relations section, Presentations and Events. Please go to the website 15 minutes prior to the start of the call to register, download, and install any necessary audio software. A replay of the conference call will be available on Theravance Biopharma’s website for 30 days through December 7, 2017. An audio replay will also be available through 8:00 pm ET on November 14, 2017 by dialing (855) 859-2056 from the U.S., or (404) 537-3406 for international callers, and then entering confirmation code 96855845. About Theravance Biopharma Theravance Biopharma is a diversified biopharmaceutical company with the core purpose of creating medicines that help improve the lives of patients suffering from serious illness. Our pipeline of internally discovered product candidates includes potential best-in-class medicines to address the unmet needs of patients being treated for serious conditions primarily in the acute care setting. VIBATIV® (telavancin), our first commercial product, is a once-daily dual-mechanism antibiotic approved in the U.S., Europe and certain other countries for certain difficult-to-treat infections. Revefenacin (TD-4208) is a long-acting muscarinic antagonist (LAMA) being developed as a potential once-daily, nebulized treatment for chronic obstructive pulmonary disease (COPD). Our neprilysin (NEP) inhibitor program is designed to develop selective NEP inhibitors for the treatment of a range of major cardiovascular and renal diseases, including acute and chronic heart failure, hypertension and chronic kidney diseases, such as diabetic nephropathy. Our research efforts are focused in the areas of inflammation and immunology, with the goal of designing medicines that provide targeted drug delivery to tissues in the lung and gastrointestinal tract in order to maximize patient benefit and minimize risk. The first program to emerge from this research is designed to develop intestinally restricted pan-Janus kinase (JAK) inhibitors for the treatment of a range of inflammatory intestinal diseases. In addition, we have an economic interest in future payments that may be made by Glaxo Group Limited or one of its affiliates (GSK) pursuant to its agreements with Innoviva, Inc. relating to certain drug development programs, including Trelegy Ellipta (the combination of fluticasone furoate, umeclidinium, and vilanterol in a single ELLIPTA® inhaler, previously referred to as the Closed Triple), currently approved in the US for the treatment of appropriate COPD patients and in development for the treatment of COPD in several other countries. The product is also currently in development for the treatment of asthma. For more information, please visit www.theravance.com. THERAVANCE®, the Cross/Star logo, and VIBATIV® are registered trademarks of the Theravance Biopharma group of companies. Trademarks, trade names or service marks of other companies appearing on this press release are the property of their respective owners. This press release contains and the conference call will contain certain “forward-looking” statements as that term is defined in the Private Securities Litigation Reform Act of 1995 regarding, among other things, statements relating to goals, plans, objectives, expectations and future events. Theravance Biopharma intends such forward-looking statements to be covered by the safe harbor provisions for forward-looking statements contained in Section 21E of the Securities Exchange Act of 1934 and the Private Securities Litigation Reform Act of 1995. Examples of such statements include statements relating to: the Company’s strategies, plans and objectives, the Company’s regulatory strategies and timing of clinical studies (including the data therefrom), the potential benefits and mechanisms of action of the Company’s product and product candidates, the Company’s expectations for product candidates through development, potential regulatory approval and commercialization (including their potential as components of combination therapies), product sales and the Company’s expectations for its 2017 operating loss, excluding share-based compensation. These statements are based on the current estimates and assumptions of the management of Theravance Biopharma as of the date of the press release and the conference call and are subject to risks, uncertainties, changes in circumstances, assumptions and other factors that may cause the actual results of Theravance Biopharma to be materially different from those reflected in the forward-looking statements. Important factors that could cause actual results to differ materially from those indicated by such forward-looking statements include, among others, risks related to: delays or difficulties in commencing, enrolling or completing clinical studies, the potential that results from clinical or non-clinical studies indicate the Company’s product candidates are unsafe or ineffective (including when our product candidates are studied in combination with other compounds), the feasibility of undertaking future clinical trials for our product candidates based on FDA policies and feedback, dependence on third parties to conduct clinical studies, delays or failure to achieve and maintain regulatory approvals for product candidates, risks of collaborating with or relying on third parties to discover, develop, manufacture and commercialize products, risks associated with establishing and maintaining sales, marketing and distribution capabilities with appropriate technical expertise and supporting infrastructure, and risks of developing an institutional customer mix for VIBATIV® (telavancin) that meet the Company’s plan for the product. Other risks affecting Theravance Biopharma are described under the heading “Risk Factors” contained in Theravance Biopharma’s Form 10-Q filed with the Securities and Exchange Commission (SEC) on August 9, 2017 and Theravance Biopharma’s other filings with the SEC. In addition to the risks described above and in Theravance Biopharma’s filings with the SEC, other unknown or unpredictable factors also could affect Theravance Biopharma’s results. No forward-looking statements can be guaranteed and actual results may differ materially from such statements. Given these uncertainties, you should not place undue reliance on these forward-looking statements. Theravance Biopharma assumes no obligation to update its forward-looking statements on account of new information, future events or otherwise, except as required by law. Contact Information: Alexander Dobbin THERAVANCE BIOPHARMA, INC. CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (In thousands, except per share data) Three Months Ended September 30, Nine Months Ended September 30, -------------------------------- ------------------------------- 2017 2016 2017 2016 ---- ---- ---- ---- (Unaudited) (Unaudited) Revenue: Product sales $4,140 $3,901 $10,664 $12,571 Revenue from collaborative arrangements 135 15,174 207 30,385 --- ------ --- ------ Total revenue 4,275 19,075 10,871 42,956 Costs and expenses: Cost of goods sold 985 332 2,914 1,748 Research and development (1) 39,343 31,951 122,835 99,698 Selling, general and administrative (1) 20,944 20,286 66,069 64,143 ------ ------ ------ ------ Total costs and expenses 61,272 52,569 191,818 165,589 ------ ------ ------- ------- Loss from operations (56,997) (33,494) (180,947) (122,633) Interest expense (2,136) - (6,410) - Other-than-temporary impairment loss (8,000) - (8,000) - Interest and other income (expense), net 1,124 344 3,579 839 ----- --- ----- --- Loss before income taxes (66,009) (33,150) (191,778) (121,794) Provision for income taxes 868 812 6,705 1,542 --- --- ----- ----- Net loss $(66,877) $(33,962) $(198,483) $(123,336) ======== ======== ========= ========= Net loss per share: Basic and diluted net loss per share $(1.27) $(0.73) $(3.80) $(2.86) ====== ====== ====== ====== Shares used to compute basic and diluted net loss per share 52,611 46,470 52,165 43,080 ====== ====== ====== ====== (1)Amounts include share-based compensation expense as follows: Three Months Ended September 30, Nine Months Ended September 30, -------------------------------- ------------------------------- (In thousands) 2017 2016 2017 2016 ------------- ---- ---- ---- ---- Research and development $5,005 $4,933 $15,023 $15,052 Selling, general and administrative 5,680 4,962 16,329 16,077 Total share-based compensation expense $10,685 $9,895 $31,352 $31,129 ======= ====== ======= =======
THERAVANCE BIOPHARMA, INC. CONDENSED CONSOLIDATED BALANCE SHEETS (In thousands) September 30, December 31, 2017 2016 ---- ---- Assets (Unaudited) (1) Current assets: Cash and cash equivalents and short-term marketable securities $335,001 $501,096 Receivables from collaborative arrangements 11,547 9,076 Prepaid taxes 289 3,060 Inventories 15,258 12,220 Other prepaid and current assets 5,038 3,051 Property and equipment, net 8,618 8,460 Long-term marketable securities 99,399 91,565 Tax receivable 8,070 - Restricted cash 833 833 Other assets 2,106 9,893 Total assets $486,159 $639,254 ======== ======== Liabilities and Shareholders’ Equity Current liabilities 48,786 49,268 Long-term liabilities 253,256 239,755 Shareholders’ equity 184,117 350,231 ------- ------- Total liabilities and shareholders’ equity $486,159 $639,254 ======== ======== ________________________________
(1) The condensed consolidated balance sheet at December 31, 2016 has been derived from the audited consolidated financial statements included in the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2016.
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Company Codes: NASDAQ-NMS:TBPH |
