HENDERSON, Nev.--(BUSINESS WIRE)--Spectrum Pharmaceuticals, Inc. (NasdaqGS: SPPI), a biotechnology company with fully integrated commercial and drug development operations with a primary focus in hematology and oncology, announced today financial results for the three-month period ended June 30, 2015.
“The results from this quarter demonstrate our ability to maintain financial discipline while continuing to fund our highest priority projects,” said Rajesh C. Shrotriya, MD, Chairman and Chief Executive Officer of Spectrum Pharmaceuticals. “The second half of 2015 marks key milestones for several of Spectrum’s drugs. With the potential approval of Evomela in October, we could have six drugs on the market. Pending alignment with the FDA, we expect to initiate a non-inferiority Phase 3 study for SPI-2012 which would be powered at 80% to show superiority against pegfilgrastim. Also, our potentially best-in-class novel pan-HER inhibitor, poziotinib, will target breast cancer in a Phase 2 clinical program. Additionally, with apaziquone, we plan to file an NDA and initiate a confirmatory Phase 3 trial under a SPA by year end. Our pipeline has never been as exciting as it is today, and provides a sound foundation for future growth of the company.”
Two Potential Blockbusters, One Near-term FDA Decision and One Near-term NDA Submission
- SPI-2012, a novel long-acting GCSF: In Phase 2 trials earlier this year, SPI-2012’s efficacy was shown to be non-inferior at the middle dose, and superior to the blockbuster drug pegfilgrastim at the higher dose tested. Based on discussion with the FDA, the Company plans to initiate a Phase 3 study this year, and is seeking an SPA for this study that would be powered at over 90% to demonstrate non-inferiority and at 80% to demonstrate superiority to pegfilgrastim.
- EVOMELA, a propylene-glycol free formulation of melphalan with improved stability: NDA review is ongoing and is on track for an FDA decision on October 23, 2015. This drug is expected to be launched using Spectrum’s existing sales force, and pre-launch activities have commenced.
- Poziotinib, a potential best-in-class, novel, pan-HER inhibitor: The Company plans to initiate a U.S. based breast cancer program based on compelling Phase 1 efficacy data demonstrated in breast cancer patients who had failed multiple other HER-2 directed therapies. In addition, multiple Phase 2 studies funded by Hanmi Pharmaceuticals are currently ongoing.
- Apaziquone, a potent pro-drug being investigated for non-muscle-invasive bladder cancer: Apaziquone is a bio-reductive agent activated by reductase enzymes, such as DT-diaphorase, expressed by bladder tumor cells, to form a cytotoxic alkylating agent. Spectrum expects to file an NDA by year-end. Additionally, the Company is seeking an SPA with the FDA before commencing an additional confirmatory Phase 3 Study.
Three-Month Period Ended June 30, 2015 (All numbers are approximate)
Total product sales were $35.1 million in the second quarter of 2015. Total product sales decreased 25% from $46.9 million in the second quarter of 2014.
Product sales in the second quarter included: FUSILEV® (levoleucovorin) net sales of $14.3 million, FOLOTYN® (pralatrexate injection) net sales of $12.2 million, ZEVALIN® (ibritumomab tiuxetan) net sales of $4.8 million, MARQIBO® (vinCRIStine sulfate LIPOSOME injection) net sales of $2.1 million and BELEODAQ® (belinostat for injection) net sales of $1.7 million.
Spectrum recorded net loss of $2.3 million, or $(0.04) per basic and diluted share in the three-month period ended June 30, 2015, compared to net loss of $3.6 million, or $(0.06) per basic and diluted share in the comparable period in 2014. Total research and development expenses were $9.6 million in the quarter, as compared to $11.3 million in the same period in 2014. Selling, general and administrative expenses were $22.6 million in the quarter, compared to $25.4 million in the same period in 2014.
Spectrum recorded non-GAAP net loss of $0.5 million, or $(0.01) per basic share and diluted share in the three-month period ended June 30, 2015, compared to non-GAAP net income of $6.8 million, or $0.11 per basic share and $0.09 per diluted share in the comparable period in 2014. Non-GAAP research and development expenses were $9.1 million, as compared to $10.8 million in the same period of 2014. Non-GAAP selling, general and administrative expenses were $19.7 million, as compared to $21.8 million in the same period in 2014.
2015 Financial Guidance
Spectrum projects year-end aggregate cash and cash equivalents and marketable securities of over $110 million, up from the Company’s previous guidance of $100 million excluding any new business development transactions.
Thursday, August 6, 2015 @ 4:30 p.m. Eastern/1:30 p.m. Pacific
Domestic: (877) 837-3910, Conference ID# 85787537
International: (973) 796-5077, Conference ID# 85787537
This conference call will also be webcast. Listeners may access the webcast, which will be available on the investor relations page of Spectrum Pharmaceuticals' website: www.sppirx.com on August 6, 2015 at 4:30 p.m. Eastern/1:30 p.m. Pacific.
About Spectrum Pharmaceuticals, Inc.
Spectrum Pharmaceuticals is a leading biotechnology company focused on acquiring, developing, and commercializing drug products, with a primary focus in hematology and oncology. Spectrum markets five hematology/oncology drugs, and expects an FDA decision on another hematology drug later this year. Additionally, Spectrum's pipeline includes three drugs targeting blockbuster markets in advanced stages of clinical development. Spectrum's strong track record in in-licensing and acquiring differentiated drugs, and expertise in clinical development have generated a robust, diversified, and growing pipeline of product candidates in advanced-stage Phase 2 and Phase 3 studies. More information on Spectrum is available at www.sppirx.com.
Evomela, a propylene glycol-free formulation of melphalan,is being investigated for the multiple myeloma transplant setting, for which it has been granted an Orphan Drug Designation by the FDA. This formulation eliminates the need to use propylene glycol containing custom diluent, which has been reported to cause renal and cardiac side effects, which in turn limit the ability to deliver higher doses of therapeutic compounds. The use of the Captisol® technology to reformulate melphalan also improves its stability and is anticipated to allow for slower infusion rates and longer administration durations, potentially enabling clinicians to safely achieve a higher dose intensity for pre-transplant chemotherapy.
Captisol is a patent-protected, chemically modified cyclodextrin with a structure designed to optimize the solubility and stability of drugs. Captisol was invented and initially developed by scientists in the laboratories of Dr. Valentino Stella at the University of Kansas’ Higuchi Biosciences Center for specific use in drug development and formulation. This unique technology has enabled six FDA-approved products, including Onyx Pharmaceuticals’ Kyprolis®, Baxter International’s Nexterone® and Merck’s NOXAFIL IV. There are also more than 30 Captisol-enabled products currently in clinical development.
Forward-looking statement - This press release may contain forward-looking statements regarding future events and the future performance of Spectrum Pharmaceuticals that involve risks and uncertainties that could cause actual results to differ materially. These statements are based on management's current beliefs and expectations. These statements include, but are not limited to, statements that relate to our business and its future, including certain company milestones, Spectrum's ability to identify, acquire, develop and commercialize a broad and diverse pipeline of late-stage clinical and commercial products, leveraging the expertise of partners and employees around the world to assist us in the execution of our strategy, and any statements that relate to the intent, belief, plans or expectations of Spectrum or its management, or that are not a statement of historical fact. Risks that could cause actual results to differ include the possibility that our existing and new drug candidates may not prove safe or effective, the possibility that our existing and new applications to the FDA and other regulatory agencies may not receive approval in a timely manner or at all, the possibility that our existing and new drug candidates, if approved, may not be more effective, safer or more cost efficient than competing drugs, the possibility that our efforts to acquire or in-license and develop additional drug candidates may fail, our lack of sustained revenue history, our limited marketing experience, our dependence on third parties for clinical trials, manufacturing, distribution and quality control and other risks that are described in further detail in the Company's reports filed with the Securities and Exchange Commission. We do not plan to update any such forward-looking statements and expressly disclaim any duty to update the information contained in this press release except as required by law.
SPECTRUM PHARMACEUTICALS, INC. ®, FUSILEV®, FOLOTYN®, ZEVALIN®, MARQIBO®, and BELEODAQ® are registered trademarks of Spectrum Pharmaceuticals, Inc and its affiliates. REDEFINING CANCER CARE™, EVOMELA™ and the Spectrum Pharmaceuticals logos are trademarks owned by Spectrum Pharmaceuticals, Inc. Any other trademarks are the property of their respective owners.
© 2015 Spectrum Pharmaceuticals, Inc. All Rights Reserved
|SPECTRUM PHARMACEUTICALS, INC.|
|Condensed Consolidated Statements of Operations|
(In thousands, except per share amounts)
Three Months Ended
Six Months Ended
|Product sales, net||$||35,144||$||46,855||$||73,557||$||86,951|
|License fees and service revenue||9,838||—||10,042||28|
|Cost of product sales (excludes amortization of purchased intangible assets)||5,990||6,156||13,061||12,434|
|Selling, general and administrative||22,552||25,399||45,886||48,802|
|Research and development||9,558||11,335||25,409||40,832|
|Amortization and impairment of intangible assets||6,916||5,361||20,938||10,721|
|Total operating costs and expenses||45,016||48,251||105,294||112,789|
|Loss from operations||(34||)||(1,396||)||(21,695||)||(25,810||)|
|Change in fair value of contingent consideration related to acquisitions||(146||)||(1,005||)||(646||)||(1,729||)|
|Other income (expense), net||69||(487||)||(966||)||(845||)|
|Total other expenses||(2,335||)||(3,468||)||(6,098||)||(6,617||)|
|Loss before income taxes||(2,369||)||(4,864||)||(27,793||)||(32,427||)|
|Benefit (provision) for income taxes||23||1,301||(115||)||1,223|
|Net loss per share:|
|Weighted average shares outstanding:|
|SPECTRUM PHARMACEUTICALS, INC.|
|Condensed Consolidated Balance Sheets|
(In thousands, expect per share and par value amounts)
|Cash and equivalents||$||142,271||$||129,942|
|Accounts receivable, net of allowance for doubtful accounts of $120 and $120, respectively||41,684||70,758|
|Deferred tax assets||172||—|
|Total current assets||207,162||222,469|
|Property and equipment, net of accumulated depreciation||1,265||1,405|
|Intangible assets, net of accumulated amortization||207,955||230,100|
|LIABILITIES AND STOCKHOLDERS’ EQUITY|
|Accounts payable and other accrued obligations||$||71,823||$||84,994|
|Accrued payroll and benefits||5,777||8,444|
|Drug development liability||573||1,141|
|Acquisition-related contingent obligations||5,243||4,901|
|Total current liabilities||90,503||109,439|
|Drug development liability, less current portion||13,916||14,644|
|Deferred revenue, less current portion||414||—|
|Acquisition-related contingent obligations, less current portion||2,745||2,441|
|Deferred tax liability||6,753||6,569|
|Other long-term liabilities||6,994||6,088|
|Convertible senior notes||98,866||96,298|
|Preferred stock, $0.001 par value; 5,000,000 shares authorized:|
|Series B junior participating preferred stock, $0.001 par value; 1,500,000 shares authorized; no shares issued and outstanding||—||—|
|Series E convertible voting preferred stock, $0.001 par value and $10,000 stated value; 2,000 shares authorized; 20 shares issued and outstanding at June 30, 2015 and December 31, 2014, respectively (convertible into 40,000 shares of common stock, with aggregate liquidation value of $240)||123||123|
|Common stock, $0.001 par value; 175,000,000 shares authorized; 67,245,602 and 65,969,699 shares issued and outstanding at June 30, 2015 and December 31, 2014, respectively||66||66|
|Additional paid-in capital||545,359||538,553|
|Accumulated other comprehensive loss||(165||)||(850||)|
|Total stockholders’ equity||234,138||254,554|
|TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY||$||454,329||$||490,033|
Non-GAAP Financial Measures
In this press release, Spectrum reports certain historical and expected non-GAAP results. Non-GAAP financial measures are reconciled to the most directly comparable GAAP financial measure in the tables of this press release and the accompanying footnotes. The non-GAAP financial measures contained herein are a supplement to the corresponding financial measures prepared in accordance with generally accepted accounting principles (GAAP). The non-GAAP financial measures presented exclude the items summarized in the below table. Management believes that adjustments for these items assist investors in making comparisons of period-to-period operating results and that these items are not indicative of the Company's on-going core operating performance.
Management uses non-GAAP net income (loss) in its evaluation of the Company's core after-tax results of operations and trends between fiscal periods and believes that these measures are important components of its internal performance measurement process. Management believes that providing these non-GAAP financial measures allows investors to view the Company's financial results in the way that management views the financial results.
The non-GAAP financial measures presented herein have certain limitations in that they do not reflect all of the costs associated with the operations of the Company's business as determined in accordance with GAAP. Therefore, investors should consider non-GAAP financial measures in addition to, and not as a substitute for, or as superior to, measures of financial performance prepared in accordance with GAAP. The non-GAAP financial measures presented by the Company may be different from the non-GAAP financial measures used by other companies.
|SPECTRUM PHARMACEUTICALS, INC.|
|Reconciliation of Non-GAAP Adjustments for Condensed Consolidated Statements of Operations|
(In thousands, expect per share amounts)
Three months ended
June 30, 2015
Six months ended
June 30, 2015
|GAAP product sales, net & license fees and service revenue||$||44,982||$||46,855||$||83,599||$||86,979|
|Non GAAP adjustments to product sales, net & license fees and service revenue:||(9,682||)||—||(9,682||)||—|
|Total adjustments to product sales, net & license fees and service revenues||(9,682||)||—||(9,682||)||—|
|Non-GAAP product sales & license and contract revenue||35,300||46,855||73,917||86,979|
|GAAP cost of product sales (excludes amortization of intangible assets)||5,990||6,156||13,061||12,434|
|Non-GAAP adjustments to cost of product sales||—||—||—||—|
|Non-GAAP cost of product sales (excludes amortization of intangible assets)||5,990||6,156||13,061||12,434|
|GAAP selling, general and administrative expenses||22,552||25,399||45,886||48,802|
|Non GAAP adjustments to SG&A:|
|Shareholder lawsuit expenses||25||(884||)||441||(1,263||)|
|Insurance reimbursement under D&O policy||365||—||1,746||—|
|Total adjustments to SG&A||(2,874||)||(3,619||)||(3,274||)||(6,650||)|
|Non-GAAP selling, general and administrative||19,678||21,780||42,612||42,152|
|GAAP research and development||9,558||11,335||25,409||40,832|
|Non-GAAP adjustments to R&D:|
|Beleodaq milestone cash payment & stock issuance||—||—||—||(17,790||)|
|Other R&D milestone payments||—||—||(3,000||)||—|
|Total adjustments to R&D||(444||)||(522||)||(3,879||)||(18,794||)|
|Non-GAAP research and development||9,114||10,813||21,530||22,038|
|GAAP amortization and impairment of intangible assets||6,916||5,361||20,938||10,721|
|Non-GAAP adjustments to amortization and impairment of intangible assets:|
|Impairment of FUSILEV distribution rights||—||—||(7,160||)||—|
|Total adjustments to amortization and impairment of intangibles||(6,916||)||(5,361||)||(20,938||)||(10,721||)|
|Non-GAAP amortization and impairment of intangibles||—||—||—||—|
|GAAP loss from operations||(34||)||(1,396||)||(21,695||)||(25,810||)|
|Non-GAAP adjustments to loss from operations||552||9,502||18,409||36,165|
|Non-GAAP income (loss) from operations||518||8,106||(3,286||)||10,355|
|GAAP total other expenses, net||(2,335||)||(3,468||)||(6,098||)||(6,617||)|
|Market-to-market of contingent consideration||146||1,005||646||1,729|
|Loss on foreign currency exchange||(127||)||—||1,019||—|
|Accretion of discount on 2018 Convertible Notes||1,298||1,185||2,569||2,332|
|Total adjustments to other expense, net||1,317||2,190||4,234||4,061|
|Non-GAAP total other expenses, net||(1,018||)||(1,278||)||(1,864||)||(2,556||)|
|GAAP benefit (provision) for income taxes||23||1,301||(115||)||1,223|
|Adjustment to benefit (provision) for income taxes||(23||)||(1,301||)||115||(1,223||)|
|Non-GAAP benefit (provision) for income taxes||—||—||—||—|
|GAAP net loss||(2,346||)||(3,563||)||(27,908||)||(31,204||)|
|Total non-GAAP adjustments||1,846||10,391||22,758||39,003|
|Non-GAAP net (loss) income||$||(500||)||$||6,828||$||(5,150||)||$||7,799|
|Non-GAAP (loss) income per share:|
|Weighted average shares outstanding:|