INNATE PHARMA: consolidated financial results for the year ended December 31, 2017
2017: CLINiCAL PROGRESS, Portfolio expansion and financial strength create the foundation for future growth
- Cash, cash equivalents and financial assets[a] amounted to €176.6m (million euros) as of December 31, 2017
- Revenue and other income amounted to €44.0m (€65.7m in 2016, including a €13.8m milestone payment from Bristol-Myers Squibb)
- Operating expenses amounted to €84.0m (€58.2m in 2016), driven by continued investment in preclinical and clinical portfolio
- Significant progress across Innate Pharma's partnered and proprietary clinical programs, with new focus on clinical development in tumor microenvironment
- Dose-escalation data show favorable safety profile and promising clinical activity for IPH4102 in patients with Sézary syndrome, an advanced form of cutanous T-cell lymphoma - cohort expansion ongoing
- Acquisition of anti-C5aR, now called IPH5401, a clinical-stage antibody, strengthens Innate's proprietary pipeline targeting the tumor microenvironment - a clinical collaboration is now underway with MedImmune
- World renowned immunologist, Professor Eric Vivier, joins Innate Pharma as Chief Scientific Officer
- Innate Pharma will hold a R&D Day for institutional investors and sell-side analysts in London today, to update on its clinical development activities
Marseille, France, March 8, 2018 - 07:00 AM CET
Innate Pharma (the "Company" - Euronext Paris: FR0010331421 - IPH) today reports its consolidated financial results for the year ended December 31, 2017. The consolidated financial statements are attached to this press release.
During 2017, Innate Pharma has made significant progress across its portfolio of partnered and proprietary programs and has laid the foundations for continued clinical development during 2018. The Company reported a favorable safety profile and encouraging clinical activity for IPH4102 in monotherapy in a Phase I trial in patients with Sézary syndrome, an advanced form of cutanous T-cell lymphoma. First data from a cohort expansion part of the ongoing trial are expected in 2018.
In June 2017, the Company strengthened its proprietary pipeline with the acquisition of IPH5401, a first-in-class anti-C5aR antibody targeting the tumor microenvironment, from Novo Nordisk A/S for a total of €40.0m (€2.8m in cash and €37.2m in new Innate Pharma shares). IPH5401 is a clinical-stage, proprietary product that reinforces Innate Pharma's position in the field of antibodies targeting the tumor microenvironment beyond the Company's existing activities in the adenosine pathway. Preclinical findings suggest that C5aR blockade increases immune-mediated tumor killing and efficacy of checkpoint inhibitors. IPH5401 will enter first clinical studies in oncology in 2018, as part of a non-exclusive clinical collaboration with MedImmune/AstraZeneca.
The Company also continued to advance its portfolio of early stage programs targeting the tumor microenvironment with two antibodies directed against enzymes in the adenosine pathway, CD39 and CD73, respectively. Preclinical experiments have demonstrated superior blocking activity of IPH52 (anti-CD39) and IPH53 (anti-CD73) for both the cell surface and soluble forms of the enzymes. Significant progress could also be recorded in the Company's collaboration with Sanofi on NK-cell bispecific engagers, who bring together tumor cells and NK cells and trigger NK cell killing of tumor cells. While the project on a first tumor target is on the way to lead candidate selection, Sanofi decided to include a second target into the framework of the collaborative agreement.
During 2017, the Company announced results from the EffiKIR study which evaluated the efficacy of lirilumab as a single agent for maintenance of remission in patients with acute myeloid leukemia. The study did not meet its primary efficacy endpoint of leukemia-free survival. Towards the end of the year, Innate's partner Bristol-Myers Squibb updated on the lirilumab program in combination with Opdivo (nivolumab) in patients with solid tumors. The assessment of efficacy did not provide an obvious development path. Discussions are ongoing regarding next steps.
After the period, Eric Vivier was appointed Chief Scientific Officer on January 8, 2018. In his new role, Professor Vivier will lead Innate Pharma's science and technology platforms as well as the development of collaborations between fundamental, translational and clinical research.
Mondher Mahjoubi, Chief Executive Officer of Innate Pharma, said: "During 2017, Innate Pharma has made significant clinical advances, within both its wholly-owned and partnered portfolios, laying the foundations for the future focus of our immuno-oncology development strategy. We expect clinical read-outs for both our monalizumab and IPH4102 program in 2018. Moreover, we are very pleased with the acquisition of IPH5401, a first-in-class anti-C5aR antibody, which strengthens our portfolio in the tumor microenvironment." He added: "We have a robust financial position, giving us the flexibility to invest for future portfolio growth. With multiple value catalysts ahead in 2018, we believe we are poised for a pivotal year."
***
Innate Pharma will host a R&D Day for institutional investors and sell-side analysts on March 8 from 1:30 to 5:00 pm GMT (8:30 to 12:00 pm ET) in London.
To join the live webcast today at 1:30pm (GMT) please use the following link:
https://www.innate-pharma.com/en/news-events/events/rd-day-2018
To join the event by conference call only, please use the following dial-in numbers:
USA: +1 646-828-8156
INTERNATIONAL: 0800 279 7204
PIN code: 3997784
The presentation will be made available on the Company's website 30 minutes before the start of the event.
A webcast replay will be available on Innate Pharma's website after the event.
***
Financial highlights for 2017:
The key elements are as follows:
- Cash, cash equivalents and financial assets amounting to €176.6m (million euros) as of December 31, 2017 (€230.7m as of December 31, 2016), including non-current financial instruments (€60.5m).
- At the same date, the financial liabilities amounted to €5.9m (€5.3m as of December 31, 2016).
- Revenue and other income amounting to €44.0m (€65.7m in 2016). This amount mainly results from licensing revenue (€32.6m) and from research tax credit (€11.0m).
- Revenue from collaboration and licensing agreements mainly results from the spreading of the initial payment received by Innate Pharma in the context of the agreement signed in April 2015 with AstraZeneca/MedImmune (€32.3m in 2017 and €41.6m in 2016).
- The 2016 revenue also included a $15m (€13.8m) milestone payment received from Bristol-Myers Squibb for the continued exploration of lirilumab in combination with nivolumab. The milestone payment followed the presentation at the SITC annual meeting (November 2016) of encouraging preliminary activity results from the cohort of patients with squamous cell carcinoma of the head and neck (SCCHN) of a Phase I/II trial. The payment was received in January 2017 and has generated an exchange gain of €0.3m.
- Operating expenses amounting to €84.0m (€58.2m in 2016) of which 80% related to research and development. The majority of the rise results from the increase in subcontracting costs in relation with the clinical development of the Company's drug candidates (+ €9.7m), in share-based payments (+ €9.0m) and in staff costs (+ €2.4m).
- A net financial loss amounting to €8.0m.
- As a consequence of the items mentioned previously, the net loss for 2017 amounts to €48.4m to be compared to a profit of €12.6m for 2016.
The table below summarizes the IFRS consolidated financial statements for fiscal year 2017, with a comparison to 2016:
Year ended December 31 | ||
In thousand euros (IFRS) | 2017 | 2016 |
Revenue from collaboration and licensing agreements | 32,631 | 56,159 |
Government financing for research expenditures | 11,402 | 9,561 |
Revenue and other income | 44,033 | 65,721 |
Research and Development expenses | (67,000) | (48,628) |
General and Administrative expenses | (17,015) | (9,522) |
Operating expenses | (84,015) | (58,150) |
Operating income / (loss) | (39,983) | 7,571 |
Financial income / (expenses), net | (8,034) | 5,370 |
Income tax | (368) | (301) |
Net income / (loss) | (48,385) | 12,640 |
Pipeline update (second half of 2017):
IPH4102 (anti-KIR3DL2 antibody):
IPH4102 is a first-in-class anti-KIR3DL2 humanized cytotoxicity-inducing antibody, designed for treatment of CTCL, an orphan disease, and in particular, its most aggressive subtypes, Sézary Syndrome and transformed mycosis fungoides.
In October 2017, the final results of the dose-escalation part of the ongoing Phase I study investigating IPH4102 in patients with relapsed/refractory cutaneous T-cell lymphoma (CTCL), an orphan disease, were presented by Pr. Martine Bagot, Principal Investigator and Head of the Dermatology Department at the Saint-Louis Hospital, Paris, in an oral session at the EORTC CLTF in London.
- These data confirm the good safety profile and promising activity of IPH4102 in this elderly and heavily pretreated patients population (n=25). The objective response rate in the 20 patients with Sézary syndrome was 50%; the rate of response lasting at least more than 4 months (ORR4) was 40%, the disease control rate (DCR), 90%, the median duration of response (DOR), 9.9 months and the median progression free survival (PFS), 10.8 months, respectively. Data on pruritus were reported for the first time and show substantial improvement in patients having a global clinical response but also in patients with stable disease. The Recommended Phase 2 Dose (RP2D) has been identified at 750 mg, a fixed dose equivalent to 10 mg/kg. Expansion cohorts started, including 2 cohorts of 15 patients each in two CTCL subtypes: Sézary syndrome and transformed mycosis fungoides.
- Biomarker results were presented in an oral presentation by Dr. Maxime Battistella, Assistant Professor Pathology and Dermatopathology at St Louis Hospital and Université L. Diderot.
- Data from a cohort expansion part of the ongoing phase I trial in patients with Sézary syndrome are expected in 2018 and will be presented at an upcoming medical conference.
IPH5401 (anti-C5aR antibody):
IPH5401 is a first-in-class fully human therapeutic antibody that specifically binds and blocks C5a receptors (C5aR) expressed on subsets of myeloid-derived suppressor cells (MDSC) and neutrophils.
- In September 2017, at the third CRI-CIMT-EATI-AACR International Cancer Immunotherapy conference, Innate Pharma has presented preclinical data that reinforce the IPH5401 rationale. This data show the selective expression of C5aR on myeloid-derived suppressor cells (MDSC) and neutrophils. These cells accumulate within the tumor microenvironment and secrete pro-angiogenic factors which promote tumor progression. They also inhibit NK and T cells and suppress anti-tumor immunity. In this poster, the data demonstrate that IPH5401 selectively inhibits the activation of neutrophils. Moreover, the data show that the combined administration of anti-C5aR with anti-PD-1 synergistically reduced tumor growth. Taken together, these data suggest that C5aR blockade may result in a more permissive environment for immune-mediated tumor killing and treatment with checkpoint inhibitors.
- IPH5401 will enter clinical studies in oncology in 2018.
Monalizumab (anti-NKG2A antibody), partnered with AstraZeneca/MedImmune:
Monalizumab is a checkpoint inhibitor targeting NKG2A, an inhibitory receptor expressed on tumor infiltrating cytotoxic CD8 T lymphocytes and NK cells. This monoclonal antibody is currently being tested in an exploratory program of Phase I or I/II clinical trials in various cancer indications in combinations in solid tumors.
- In September 2017, the Company presented new preclinical data at the third CRI-CIMT-EATI-AACR International Cancer Immunotherapy conference that reinforce the rationale, that combined NKG2A/HLA-E and PD-1/PD-L1 blockade enhance CD8+ T Cell-mediated killing of tumors.
- First clinical data read-outs from the Phase I/II trial in advanced solid tumors are expected in the course of 2018 and will be presented at upcoming medical conferences.
Lirilumab (anti-KIR antibody), licensed to Bristol-Myers Squibb:
Lirilumab is a fully human monoclonal antibody that is designed to block the interaction between KIR2DL-1,-2,-3 inhibitory receptors and their ligands. Blocking these receptors facilitates activation of NK cells and, potentially some subsets of T cells, ultimately leading to destruction of tumor cells.
- In November 2017, Innate Pharma provided an update on the clinical study program of lirilumab, licensed to Bristol-Myers Squibb. While lirilumab was shown to be well-tolerated, the assessment of efficacy from the ongoing exploration of doublet combinations, notably the nivolumab combination in an extended population of SCCHN patients, did not provide clear evidence of benefit to patients or an obvious development path. Discussions are ongoing regarding next steps for the program.
- In December 2017, full data for EffiKIR[b] study have been disclosed in an oral presentation by Pr. Norbert Vey, Team leader Translational Medicine - Hematology at the Paoli-Calmettes Institute (IPC), at the ASH annual meeting. These data suggest that alternate dosing regimens, where KIR receptors are not permanently occupied and allow the interaction with their cognate ligands during maturation, could be worth exploring.
IPH52 (anti-CD39 antibody) and IPH53 (anti-CD73[c] antibody):
CD39 and CD73 are membrane-bound extracellular enzyme which play a major role in promoting immunosuppression through the pathway degrading adenosine triphosphate (ATP) into adenosine. The blockade of CD39 and CD73 has the potential to promote anti-tumor immune responses across a wide range of tumors.
In November 2017, preclinical data for IPH52 and IPH53 were presented at the Immune Checkpoint Inhibitors Summit in Munich. These data demonstrate the expression of CD39 and CD73 in the tumor microenvironment, the blockade rationale in tumor models, especially in combination with checkpoint inhibitors, as well as the efficacy in blocking the ATP/Adenosine pathway.
Corporate update:
In January 2018, Innate Pharma announced the appointment of Prof. Eric Vivier as Chief Scientific Officer of the Company.
Also in January, the Company announced the appointment of Prof. Jean-Yves Blay to the Innate Pharma's Supervisory Board. Additionally, Marcus Schindler, SVP and Head of External Innovation and Strategy at Novo Nordisk A/S has replaced Karsten Munk Knudsen as Novo Nordisk A/S' s permanent representative on the Supervisory Board effective March 7, 2018. Karsten Munk Knudsen was appointed Executive Vice President & Chief Financial Officer of Novo Nordisk A/S on February 15, 2018.
In 2017, Innate Pharma recruited 34 new people, mostly in research and development, to support the expansion of the preclinical portfolio and the increase in the number of clinical trials performed by the Company. As at December 31, 2017, the headcount was 188 employees.
Post period events:
Clinical collaborations:
On January 30, the Company announced a non-exclusive clinical trial collaboration with MedImmune, the global biologics research and development arm of AstraZeneca. The Phase I/II study (STELLAR-001) will evaluate the safety and efficacy of durvalumab, an anti-PD-L1 immune checkpoint inhibitor, in combination with Innate's investigational first-in-class anti-C5aR monoclonal antibody, IPH5401, as a treatment for patients with selected solid tumors. Innate will sponsor the study with costs equally shared by both parties.
Next scientific publications:
Innate Pharma will present a broad range of preclinical and clinical data on on its development portfolio at the AACR 2018 Annual Meeting being held April 14 - 18, 2018, in Chicago, Illinois. Abstracts will be available on the conference website on March 14 after 4:30 p.m. U.S. ET.
About Innate Pharma:
Innate Pharma S.A. is a clinical-stage biotechnology company with a focus on discovering and developing first-in-class therapeutic antibodies that harness the innate immune system to improve cancer treatment and clinical outcomes for patients.
Innate Pharma specializes in immuno-oncology, a new therapeutic field that is changing cancer treatment by mobilizing the power of the body's immune system to recognize and kill cancer cells.
The Company's aim is to become a fully-integrated biopharmaceutical company in the area of immunotherapy and focused on serious unmet medical needs in cancer. Innate Pharma has pioneered the discovery and development of checkpoint inhibitors to activate the innate immune system. Innate Pharma's innovative approach has resulted in three first-in-class, clinical-stage antibodies targeting natural killer cell receptors that may address a broad range of solid and hematological cancer indications as well as additional preclinical product candidates and technologies. Targeting receptors involved in innate immunity also creates opportunities for the Company to develop therapies for inflammatory diseases.
The Company's expertise and understanding of natural killer cell biology have enabled it to enter into major alliances with leaders in the biopharmaceutical industry including AstraZeneca, Bristol-Myers Squibb and Sanofi.
Based in Marseille, France, Innate Pharma has more than 180 employees and is listed on Euronext Paris.
Learn more about Innate Pharma at www.innate-pharma.com.
Information about Innate Pharma shares:
ISIN code Ticker code | FR0010331421 IPH |
Disclaimer:
This press release contains certain forward-looking statements. Although the company believes its expectations are based on reasonable assumptions, these forward-looking statements are subject to numerous risks and uncertainties, which could cause actual results to differ materially from those anticipated. For a discussion of risks and uncertainties which could cause the company's actual results, financial condition, performance or achievements to differ from those contained in the forward-looking statements, please refer to the Risk Factors ("Facteurs de Risque") section of the Document de Reference prospectus filed with the AMF, which is available on the AMF website (http://www.amf-france.org) or on Innate Pharma's website.
This press release and the information contained herein do not constitute an offer to sell or a solicitation of an offer to buy or subscribe to shares in Innate Pharma in any country.
For additional information, please contact:
Investors Innate Pharma Markus Metzger / Jérôme Marino Investor relations Tel.: +33 (0)4 30 30 30 30 investors@innate-pharma.com | International Media Consilium Strategic Communications Mary-Jane Elliott / Jessica Hodgson Tel.: +44 (0)20 3709 5700 InnatePharma@consilium-comms.com |
French Media ATCG Press Marie Puvieux Mob: +33 (0)6 10 54 36 72 presse@atcg-partners.com |
APPENDIX
Innate Pharma SA
Consolidated financial statements
at December 31, 2017
The following consolidated balance sheet, income statement and statement of cash flows are prepared in accordance with International Financial Reporting Standards.
The audit procedures on the consolidated financial statements have been performed. The auditors' report will be issued after the finalization of the required procedures relating to the filing of the annual report ('Document de Référence'). The consolidated financial statements were approved by the Company's Executive board on March 7, 2018. These statements were reviewed by the Company's Supervisory board on March 7, 2018 and will be submitted for approval to the Shareholders' General Meeting on May 29, 2018.
Innate Pharma's financial annual report, included in the reference document, will be available during the second quarter of 2017.
Statement of financial position
(in thousand euros)
Year ended December 31, | ||
2017 | 2016 | |
Assets | ||
Current assets | ||
Cash and cash equivalents | 99,367 | 175,906 |
Short term investments | 16,743 | 21,782 |
Current receivables | 21,412 | 32,390 |
Total current assets | 137,521 | 230,078 |
Non-current assets | ||
Intangible assets | 46,192 | 9,075 |
Tangible assets | 10,729 | 9,094 |
Non-current financial assets | 60,469 | 32,975 |
Other non-current financial assets | 111 | 355 |
Total non-current assets | 117,501 | 51,499 |
Total assets | 255,023 | 281,577 |
Liabilities | ||
Current liabilities | ||
Trade payables | 24,657 | 20,265 |
Financial liabilities - current portion | 1,343 | 1,264 |
Deferred revenue - current portion | 47,909 | 54,912 |
Total current liabilities | 73,909 | 76,441 |
Non-current liabilities | ||
Financial liabilities - non-current portion | 4,521 | 4,063 |
Defined benefit obligations | 2,621 | 2,418 |
Deferred revenue - non-current portion | 87,005 | 112,348 |
Provisions | 1,012 | 136 |
Total non-current liabilities | 95,158 | 118,965 |
Shareholders' equity attributable to equity holders of the Company | ||
Share capital | 2,880 | 2,696 |
Share premium | 234,874 | 187,571 |
Consolidated reserves | (103,595) | (116,235) |
Net income (loss) | (48,385) | 12,640 |
Other reserves | 180 | (503) |
Total shareholders' equity attributable to equity holders of the Company | 85,956 | 86,169 |
Total liabilities and equity | 255,023 | 281,577 |
Statement of income (loss)
(in thousand euros)
Year ended December 31, | |||
2017 | 2016 | ||
Revenue from collaboration and licensing agreements | 32,631 | 56,159 | |
Government financing for research expenditures | 11,402 | 9,561 | |
Revenue and other income | 44,033 | 65,721 | |
Research and development | (67,000) | (48,628) | |
General and administrative | (17,015) | (9,522) | |
Net operating expenses | (84,015) | (58,150) | |
Operating income (loss) | (39,983) | 7,571 | |
Financial income | 2,482 | 7,327 | |
Financial expenses | (10,516) | (1,957) | |
Net income (loss) before tax | (48,016) | 12,941 | |
Income tax expense | (368) | (301) | |
Net income (loss) | (48,385) | 12,640 | |
Net income (loss) per share attributable to equity holders of the Company: | |||
Weighted average number of shares (in thousand): | 54,352 | 53,869 | |
(in € per share) | |||
- Basic loss per share | (0.89) | 0.23 | |
- Diluted loss per share | (0.89) | 0.23 |
Statement of cash flows
(in thousand euros)
Year ended December 31, | |||
2017 | 2016 | ||
Net income (loss) | (48,385) | 12,640 | |
Depreciation and amortization | 4,393 | 3,263 | |
Provisions for defined benefit obligations | 381 | 609 | |
Provisions for charges | 877 | 136 | |
Share-based compensation expense | 9,829 | 1,031 | |
Change in valuation allowance on financial assets | (26) | (826) | |
Gains (losses) on financial assets | 3,381 | (834) | |
Change in valuation allowance on financial instruments | (204) | (183) | |
Gains on assets and other financial assets | (1,442) | (1,699) | |
Interest paid | 113 | 124 | |
Others | - | (324) | |
Operating cash flow before change in working capital | (31,080) | (13,937) | |
Change in working capital | (16,980) | (50,788) | |
Net cash generated from / (used in) operating activities | (48,060) | (36,851) | |
Acquisition of property and equipment | (2,964) | (1,350) | |
Acquisition of intangible assets | (3,062) | (8,043) | |
Purchase of current financial instruments | (2,543) | (16,629) | |
Purchase of non-current financial instruments | (40,729) | (1,525) | |
Disposal of current financial instruments | 5,646 | 78,565 | |
Disposal of non-current financial instruments | 12,750 | 7,793 | |
Gains on assets and other financial assets | 1,442 | 1,699 | |
Net cash generated from / (used in) investing activities | (29,460) | 60,510 | |
Proceeds from the exercise / subscription of equity instrument | 491 | 193 | |
Proceeds from new loans | 1,739 | - | |
Repayment of financial liabilities | (1,202) | (685) | |
Interest paid | (113) | (124) | |
Purchase/sale of treasury shares | - | 14 | |
Net cash generated from / (used in) financing activities | 915 | (602) | |
Effect of the exchange rate changes | 68 | (23) | |
Net increase / (decrease) in cash and cash equivalents | (76,539) | 23,036 | |
Cash and cash equivalents at the beginning of the year | 175,906 | 152,870 | |
Cash and cash equivalents at the end of the year | 99,367 | 175,906 |
Management discussion on annual results for 2017:
Revenue and other income
Revenue and other income result from government financing for research expenditure and collaboration and licensing agreements. The Company's revenue and other income were €65.7 million and €44.0 million for the fiscal years ended December 31, 2016 and 2017, from the following sources:
Year ended December 31 (in thousand euros) | 2017 | 2016 |
Revenue from collaboration and licensing agreements | 32,631 | 56,159 |
Government financing for research expenditures | 11,402 | 9,561 |
Revenue and other income | 44,033 | 65,721 |
Revenue from collaboration and licensing agreements
Revenue from collaboration and licensing agreements amounted to €56.2 million and €32.6 million for the fiscal years ended December 31, 2016 and 2017, respectively. These revenues result from the agreements signed with Bristol-Myers Squibb in July 2011 (for 2016 only) and AstraZeneca in April 2015.
Following the licensing agreement signed with Bristol-Myers Squibb for the development and commercialization of the drug candidate lirilumab (July 2011), the Company received an upfront payment of €24.9 million ($35.3 million). This upfront payment, which is non-refundable and non-creditable, was recognized in turnover during the expected period of duration of the clinical program in course at the date of the contract. The amount recognized as revenue amounted to €0.4 million for the fiscal year 2016. This payment was entirely recognized in revenue as of June 30, 2016.
Following the presentation at the SITC annual meeting (November 2016) of preliminary activity results from the cohort of patients with SCCHN of a Phase I/II trial, the Company has been eligible to a milestone payment of $15 million (€13.8 million). The consideration was received in January 2017 but principaly recognized as revenue in 2016, since the trigger event occurred in 2016. The payment received in 2017 has generated an exchange gain of €0.3m.
The Company entered into a global co-development and commercialization agreement with AstraZeneca for monalizumab in April 2015. The Company received an initial payment amounting to $250 million on June 30, 2015. The recognition of this amount is based on the costs Innate Pharma is engaged to bear in the context of the agreement. The amount recognized for the fiscal year 2016 amounts to €41.6 million and €32.3 million for the fiscal year 2017. The percentage of completion has been determined on the basis of the costs recognized during the period compared to the total expected costs. As of December 31, 2017, the amount not yet in revenue amounts to €134.9 million (€47.9 million as "Operational liabilities" and €87.0 million as "Other non-current liabilities").
Consequently, the fall of the turnover in 2017 results from both the revenue relating to Bristol-Myers Squibb agreement (€14.3 million decrease) and the AstraZeneca agreement (€9.2 million decrease).
Government funding for research expenditures
The table below details government financing for research expenditure for the fiscal years ended December 31, 2016 and 2017:
By: Nasdaq / GlobeNewswire
- 08 Mar 2018
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