Aratana Therapeutics Reports Second Quarter 2018 Financial Results
LEAWOOD, Kan., Aug. 2, 2018 /PRNewswire/ -- Aratana Therapeutics, Inc. (Nasdaq: PETX), a pet therapeutics company focused on the licensing, development and commercialization of innovative therapeutics for dogs and cats, announced its second quarter 2018 financial results. For the second quarter ended June 30, 2018, Aratana reported total net revenues of $4.9 million and a net loss of $6.4 million or $0.14 diluted loss per share.
"We believe that our therapeutics, Entyce, Nocita and Galliprant, are helping to elevate the standard of care in veterinary medicine as is evident from the strong clinic uptake, quarter-over-quarter growth and enthusiasm expressed to us by veterinarians," stated Steven St. Peter, M.D., President and Chief Executive Officer of Aratana Therapeutics. "Our commercial organization continues to concentrate on expanding our access to target accounts and growing same clinic revenue."
- Aratana recorded ENTYCE® (capromorelin oral solution) net product sales of $1.3 million in the second quarter of 2018. Approximately 10,000 veterinary clinics in the United States have ordered ENTYCE, an appetite stimulant for dogs, and more than half of ENTYCE customers re-ordered in the second quarter of 2018. In the accounts targeted by Aratana's therapeutic specialists (sales representatives) in the second quarter of 2018, net sales were 250 percent higher as compared to non-targeted accounts. Additionally, within targeted accounts, we observed a positive correlation between the number of interactions (educational events or promotion by our therapeutic specialists) and ENTYCE net sales. Hence, in the second half of the year, Aratana plans to continue educational efforts in targeted accounts to increase the frequency of use and duration of therapy.
- In the second quarter of 2018, the Company reported $1.8 million of NOCITA® (bupivacaine liposome injectable suspension) net product sales. The therapeutic, which provides local post-operative analgesia for up to 72 hours following cranial cruciate ligament surgery in dogs, continues to show quarter-over-quarter sequential growth due to strong re-order rates, brand awareness and satisfaction among surgeons.
- In July 2018, Aratana announced it amended its agreements with the supplier of NOCITA, Pacira Pharmaceuticals, Inc., to include a 10 mL vial size. Aratana believes a 10 mL vial has the potential to be used by veterinarians for dosing smaller dogs. The Company anticipates commencing the FDA post-approval submission process and if approved, Aratana anticipates NOCITA could be available to veterinarians in a 10 mL vial size in the fall of 2019.
- Aratana recorded $1.9 million in licensing and collaboration revenue in the second quarter of 2018 for GALLIPRANT® (grapiprant tablets), which was generated from Elanco Animal Health (a division of Eli Lilly & Co.) recording approximately $10 million in net product sales. According to third-party market research conducted in June 2018, GALLIPRANT, which is for the control of pain and inflammation associated with osteoarthritis in dogs, continues to grow market share in a competitive category and is the second-leading NSAID prescribed by veterinarians. Assuming GALLIPRANT quarterly sales trends remain consistent, Aratana expects to achieve a $15.0 million commercial milestone in 2018.
The second quarter 2018 net loss was $6.4 million or $0.14 diluted loss per share compared to a net loss of $10.4 million or $0.26 diluted loss per share for the corresponding quarter of 2017. Aratana reported $4.9 million in net revenues for the quarter ended June 30, 2018 compared to $5.2 million in net revenues in the second quarter of 2017. In the second quarter of 2018, the Company recognized $1.8 million in net product sales of NOCITA, $1.3 million in net product sales of ENTYCE and $1.9 million in licensing and collaboration revenue from Elanco for GALLIPRANT. In comparison, net revenues in the second quarter of 2017 included $3.7 million in product sales of finished goods sold to Elanco, $0.8 million in licensing and collaboration revenue from Elanco for GALLIPRANT and $0.6 million in net product sales of NOCITA.
The cost of product sales totaled $1.3 million in the second quarter of 2018 in comparison to $3.7 million in the corresponding period in 2017. The decrease year-over-year in cost of product sales was primarily due to Elanco assuming responsibility for GALLIPRANT manufacturing.
Research and development expenses totaled $1.6 million in the second quarter of 2018 compared to $3.7 million for the corresponding quarter ended June 30, 2017. The decrease in research and development expenses was primarily due to fewer on-going pivotal studies compared to the corresponding period in 2017.
Selling, general and administrative expenses totaled $6.7 million for the second quarter ended June 30, 2018 compared to $6.9 million for the same period in 2017.
As of June 30, 2018, Aratana had approximately $60.4 million in cash, cash equivalents, restricted cash and short-term investments, which includes net proceeds in the second quarter from its at-the-market sales agreement of approximately $3.8 million. Consistent with previous guidance, for the remainder of 2018, the Company expects approximately $15 million of additional cash to be used for on-going operations, as well as another approximately $9.8 million of cash to be used to cover its existing debt principal obligations for the remainder of the year.
Webcast & Conference Call Details
The Company will host a live conference call on Friday, August 3, 2018 at 8:30 a.m. ET to discuss financial results from the second quarter ended June 30, 2018.
Interested participants and investors may access the audio webcast or use the conference call dial-in:
1 (866) 364-3820 (U.S.)
1 (855) 669-9657 (Canada)
1 (412) 902-4210 (International)
A replay of the second quarter 2018 results teleconference will be available the same day of the event by approximately 11 a.m. ET and an audio webcast will be accessible for 90 days in the Aratana Investor Room. For a replay of the call, use the below dial-in and conference ID 10122186:
1 (877) 344-7529 (U.S.)
1 (855) 669-9658 (Canada)
1 (412) 317-0088 (International)
About Aratana Therapeutics
Aratana Therapeutics is a pet therapeutics company focused on licensing, developing and commercializing innovative therapeutics for dogs and cats. As a pioneer in pet therapeutics, Aratana's mission is to deliver safe and effective therapeutics that elevate the standard of care in veterinary medicine. We work with companion animal veterinarians to bring new therapeutics to market that support the needs of pets and their owners. For more information, please visit www.aratana.com.
IMPORTANT SAFETY INFORMATION
GALLIPRANT® (grapiprant tablets) is not for use in humans. For use in dogs only. Keep this and all medications out of reach of children and pets. Store out of reach of dogs and other pets in a secured location in order to prevent accidental ingestion or overdose. Do not use in dogs that have a hypersensitivity to grapiprant. If Galliprant is used long term, appropriate monitoring is recommended. Concomitant use of Galliprant with other anti-inflammatory drugs, such as COX-inhibiting NSAIDs or corticosteroids, should be avoided. Concurrent use with other anti-inflammatory drugs or protein-bound drugs has not been studied. The safe use of Galliprant has not been evaluated in dogs younger than 9 months of age and less than 8 lbs (3.6 kg), dogs used for breeding, pregnant or lactating dogs, or dogs with cardiac disease. The most common adverse reactions were vomiting, diarrhea, decreased appetite, and lethargy. Please see full product label or call 1-888-545-5973 for full prescribing information.
ENTYCE® (capromorelin oral solution) is for use in dogs only. Do not use in breeding, pregnant or lactating dogs. Use with caution in dogs with hepatic dysfunction or renal insufficiency. Adverse reactions in dogs may include diarrhea, vomiting, polydipsia, and hypersalivation. Should not be used in dogs that have a hypersensitivity to capromorelin. Please see the full Prescribing Information for more detail.
NOCITA® (bupivacaine liposome injectable suspension) is for local infiltration injection in dogs only. Do not use in dogs younger than 5 months of age, dogs that are pregnant, lactating or intended for breeding. Do not administer by intravenous or intra?arterial injection. Adverse reactions in dogs may include discharge from incision, incisional inflammation and vomiting. Avoid concurrent use with bupivacaine HCl, lidocaine or other amide local anesthetics. Please see the full Prescribing Information for more detail.
Forward-Looking Statements Disclaimer
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including without limitation statements with respect to anticipated financial performance; our anticipated use of cash in the remainder of 2018; our ability to bring innovative therapeutics to the market; steps necessary for and timing of regulatory submissions and approvals of therapeutic candidates; study, development and commercialization of therapeutics or therapeutic candidates; timing of anticipated study results; increased market recognition of and demand for our therapeutics; potential use and timing of availability of the 10 mL vial size of NOCITA; expectations regarding trends in selling, general and administrative expenses; and statements regarding the Company's efforts, plans and opportunities, including, without limitation, advancing our therapeutic candidates and offering innovative therapeutics that help manage pet's medical needs safely and effectively and that result in longer and improved quality of life for pets.
These forward-looking statements are based on management's current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: our history of operating losses and our expectation that we will continue to incur losses for the foreseeable future; failure to obtain sufficient capital to fund our operations; risks relating to the impairment of intangible assets; risks pertaining to stockholder class action lawsuits; unstable market and economic conditions; restrictions on our financial flexibility due to the terms of our credit facility; our substantial dependence upon the commercial success of our therapeutics; development of our biologic therapeutic candidates is dependent upon relatively novel technologies and uncertain regulatory pathways, and biologics may not be commercially viable; denial or delay of regulatory approval for our existing or future therapeutic candidates; failure of our therapeutic candidates that receive regulatory approval to achieve market acceptance or achieve commercial success; product liability lawsuits that could cause us to incur substantial liabilities and limit commercialization of current and future therapeutics; failure to realize anticipated benefits of our acquisitions and difficulties associated with integrating the acquired businesses; development of pet therapeutics is a lengthy and expensive process with an uncertain outcome; competition in the pet therapeutics market, including from generic alternatives to our therapeutic candidates, and failure to compete effectively; failure to identify, license or acquire, develop and commercialize additional therapeutic candidates; failure to attract and retain senior management and key scientific personnel; our reliance on third-party manufacturers, suppliers and partners; regulatory restrictions on the marketing of our approved therapeutics and therapeutic candidates; our small commercial sales organization, and any failure to create a sales force or collaborate with third-parties to commercialize our approved therapeutics and therapeutic candidates; difficulties in managing the growth of our company; significant costs of being a public company; risks related to the effectiveness of our internal controls; changes in distribution channels for pet therapeutics; consolidation of our veterinarian customers; limitations on our ability to use our net operating loss carryforwards; the impact of tax reform legislation; impacts of generic products; safety or efficacy concerns with respect to our therapeutic candidates; effects of system failures or security breaches; delay or termination of the development of grapiprant therapeutic candidates and commercialization of grapiprant products that may arise from termination of or failure to perform under the collaboration agreement and/or the co-promotion agreement with Elanco; failure to obtain ownership of issued patents covering our therapeutic candidates or failure to prosecute or enforce licensed patents; failure to comply with our obligations under our license agreements; effects of patent or other intellectual property lawsuits; failure to protect our intellectual property; changing patent laws and regulations; non-compliance with any legal or regulatory requirements; litigation resulting from the misuse of our confidential information; the uncertainty of the regulatory approval process and the costs associated with government regulation of our therapeutic candidates; failure to obtain regulatory approvals in foreign jurisdictions; effects of legislative or regulatory reform with respect to pet therapeutics; the volatility of the price of our common stock; our status as an emerging growth company, which could make our common stock less attractive to investors; dilution of our common stock as a result of future financings; the influence of certain significant stockholders over our business; and provisions in our charter documents and under Delaware law could delay or prevent a change in control. These and other important factors discussed under the caption "Risk Factors" in the Company's Annual Report on Form 10-K filed with the Securities and Exchange Commission, or SEC, on March 14, 2018, along with our other reports filed with the SEC could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, we disclaim any obligation to do so, even if subsequent events cause our views to change, except as required under applicable law. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.
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ARATANA THERAPEUTICS, INC. Consolidated Statements of Operations (Unaudited) (Amounts in thousands, except share and per share data) Three Months Ended Six Months Ended June 30, June 30, -------- -------- 2018 2017 2018 2017 ---- ---- ---- ---- Revenues Licensing and collaboration revenue $1,891 $804 $3,597 $1,707 Product sales 3,017 4,354 5,354 7,246 ----- ----- ----- ----- Total revenues 4,908 5,158 8,951 8,953 ----- ----- ----- ----- Costs and expenses Cost of product sales 1,305 3,691 1,841 6,785 Royalty expense 915 353 1,721 676 Research and development 1,576 3,700 3,781 8,354 Selling, general and administrative 6,709 6,918 14,408 14,413 Amortization of intangible assets 129 86 259 150 In-process research and development - - 500 - --- --- --- --- Total costs and expenses 10,634 14,748 22,510 30,378 ------ ------ ------ ------ Loss from operations (5,726) (9,590) (13,559) (21,425) Other income (expense) Interest income 141 88 282 173 Interest expense (788) (871) (1,641) (1,731) Other expense, net - (7) (3) (9) --- --- --- --- Total other expense (647) (790) (1,362) (1,567) ---- ---- ------ ------ Net loss $(6,373) $(10,380) $(14,921) $(22,992) ======= ======== ======== ======== Net loss per share, basic and diluted $(0.14) $(0.26) $(0.33) $(0.60) Weighted average shares outstanding, 46,258,395 40,206,042 45,527,293 38,486,329 basic and diluted
ARATANA THERAPEUTICS, INC. Consolidated Balance Sheets (Unaudited) (Amounts in thousands) June 30, 2018 December 31, 2017 ------------- ----------------- Assets Current assets: Cash, cash equivalents and short-term investments $60,034 $67,615 Accounts receivable, net and prepaid expenses and other 3,763 4,048 current assets Inventories 15,196 13,576 Total current assets 78,993 85,239 Property and equipment, net 929 1,166 Goodwill 40,846 41,295 Intangible assets, net 6,357 6,616 Restricted cash 350 350 Other long-term assets 502 526 Total assets $127,977 $135,192 ======== ======== Liabilities and Stockholders' Equity Current liabilities: Accounts payable, accrued expenses and other current $4,595 $11,163 liabilities Licensing and collaboration commitment 200 7,000 Current portion - loans payable 21,333 17,333 ------ ------ Total current liabilities 26,128 35,496 Loans payable, net 8,271 19,492 Other long-term liabilities 64 70 --- --- Total liabilities 34,463 55,058 ------ ------ Total stockholders' equity 93,514 80,134 ------ ------ Total liabilities and stockholders' equity $127,977 $135,192 ======== ========
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SOURCE Aratana Therapeutics
Company Codes: NASDAQ-NMS:PETX