Montag, 30.04.2018 07:05 von GlobeNewswire | Aufrufe: 185

Curetis Publishes Full-Year 2017 Financial Results and Updated Guidance For 2018

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Curetis / Curetis Publishes Full-Year 2017 Financial Results and Updated Guidance For 2018 . Processed and transmitted by Nasdaq Corporate Solutions. The issuer is solely responsible for the content of this announcement.

 

Curetis Publishes Full-Year 2017 Financial Results and Updated Guidance For 2018

- Received U.S. FDA clearance for Unyvero System and Unyvero LRT Cartridge; commercial U.S. roll-out initiated

- Launched two novel CE-IVD marked Unyvero Applications

- Strengthened global commercial footprint; expanded installed base

Amsterdam, the Netherlands, and Holzgerlingen, Germany, April 30, 2018 - 01:00 am EDT-- Curetis N.V. (the "Company" and, together with Curetis GmbH, "Curetis"), a developer of next-level molecular diagnostic solutions, today announced financial results for the twelve months ended December 31, 2017 and provided an updated guidance for 2018.

Operational Highlights 2017 up to and including April 2018

  • De Novo request for Curetis' Unyvero System and Unyvero LRT Application granted by U.S. FDA on April 3, 2018;
  • Completed build-out of commercial team and initiated commercial roll-out of Unyvero LRT Application in the U.S.;
  • Launched novel CE-IVD marked Unyvero Application Cartridges for Intra-Abdominal Infections (Unyvero IAI) and, most recently, Urinary Tract Infection (Unyvero UTI);
  • Established U.S. Scientific Advisory Board to provide scientific counsel on advancing the development of pipeline programs for the U.S. market;
  • Raised additional capital of EUR 4.1 million via private share placements and with access to additional USD 10 million in equity over 36 months;
  • Received approval from the Singapore Health Science Authority for the Unyvero HPN and BCU Application Cartridges;
  • Signed strategic agreement in form of a memorandum of understanding with MGI (a BGI Group company, China) to leverage Curetis' sample preparation technology and to enable short-term commercialization of NGS-based molecular microbiology;
  • Awarded grant funding commitment from Austrian Research Promotion Agency (FFG) for Ares Genetics' project 'The Digital Microbe' with total project volume of EUR 1.6 million; 
  • Increased global installed base of Unyvero Analyzers by 33 to 175 by year-end of 2017, a 23% growth rate from 142 Analyzers at the end of 2016.[1] With completion of a pharmaceutical partners' clinical trial, the Company has in Q1-2018 bought back Unyvero Systems deployed in this clinical trial and has continuously taken a stronger focus on higher priority accounts and conversion efficiency, which led to a re-deployment of Unyvero Systems resulting in a temporary decrease to 167 Analyzers by the end of the first quarter 2018;
  • Initiated second U.S. FDA study to obtain clearance for the Unyvero IJI Invasive Joint Infections Application Cartridge;
  • Partnered with Biotest to support academic PEPPER Pentaglobin® Peritonitis trial with Unyvero IAI Application Cartridge;
  • Strengthened Supervisory Board with the appointment of Dr. Nils Clausnitzer, MD, MBA, elected at the 2017 AGM;
  • Founded wholly-owned subsidiary Ares Genetics in Vienna, Austria, to advance the business building on the GEAR database asset acquired form Siemens in September 2016.

2017 Key Financials


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  • Revenues: EUR 1.2 million (EUR 1.3 million in 2016). 1
  • Expenses: EUR 20.1 million total cost of sales, distribution costs, administrative expenses and research & development expenses (EUR 16.7 million in 2016).
  • Operating loss: EUR -18.6 million in 2017 due to the costs of the commercial expansion, R&D and pipeline expansion efforts (EUR -15.2 million in 2016).
  • Net loss: EUR -19.3 million (EUR -15.2 million in 2016).
  • Cash & cash equivalents: EUR 16.3 million as of December 31, 2017 (EUR 22.8 million as of December 31, 2016).1
  • Net cash burn from operating activities: EUR -15.7 million in 2017 (EUR -15.7 million in 2016).
  • Net cash burn from investing activities: EUR -0.4 million in 2017 (EUR -7.4 million in 2016), mainly resulting from the acquisitions of the GEAR database and Gyronimo platform in 2016.

             
Commenting on Curetis' 2017 results, Curetis' CEO Oliver Schacht, stated: "In 2017, we believe we have paved the way for accelerated future growth and expansion of Curetis' capabilities. This includes the completion of our integration of the GEAR and Gyronimo (now ARESdb and Unyvero A30 RQ, respectively) asset acquisitions to build a truly versatile 'any-plex' platform, which covers a broad range of infectious disease diagnostics. Moreover, we have focused on the clearance of our Unyvero Platform and Unyvero LRT Cartridge in the U.S. and invested in qualified and experienced personnel to initiate the commercial U.S. roll-out of these products immediately following their clearance. The recent U.S. FDA clearance marks a major milestone in expanding our global commercial footprint into one of the largest and most important diagnostics markets worldwide. We are confident in our U.S. roll-out strategy and remain dedicated to achieving a number of additional milestones throughout the year."

Anticipated Milestones and 2018 Guidance

Commercial Operations

  • Curetis plans to continue its EMEA commercial conversion campaign and to roll out new products (e.g. the recently launched Unyvero UTI Cartridge for urinary tract infections and the A30 RQ Platform, which will be further developed in 2018 and which is expected to be marketed under CE-mark in 2019) and plans to grow the installed base of Unyvero Analyzers and, upon commercial conversion of accounts, cartridge utilization on such installed base.
     
  • Following the clearance of the Unyvero System and the Unyvero LRT Application Cartridge by the U.S. FDA in April 2018, the Company has initiated the commercial launch of the products in the U.S. in Q2-2018, with the goal of increasing the global installed base of Unyvero Analyzers. Based on an expected U.S. sales cycle of six to nine months, sales of the LRT Application Cartridge are anticipated to ramp up by the end of 2018. In this context, Curetis expects to experience positive revenue effects towards the end of 2018 and going forward.
     
  • The Company also strives to continuously evolve and expand its commercial distribution network across those EMEA markets that are not covered by direct sales and marketing teams. To that end, Curetis has recently hired Eneko Goya as Global Commercial Partner Manager, who has longstanding experience in sales and business development, to manage and expand the global commercial partner distribution channel.
     
  • In line with the geographic expansion, in particular to the U.S. market and the further commercial roll-out in the markets covered directly or through distribution partners, the Company expects to significantly increase its global installed base of Unyvero Analyzers throughout 2018 and beyond. Starting from 175 Analyzers installed as of December 31, 2017, Curetis in Q1-2018 exercised a buy-back option for several Analyzers previously used in a by now successfully completed clinical trial (Amikacin Phase III trial) by a pharmaceutical industry partner. Further, under new commercial leadership in the EMEA region, the direct sales strategy has taken a reinforced focus on higher priority accounts and commercial conversion effectiveness, which led to a temporary re-deployment and a temporary decreased number of the global installed base to 167 Analyzers by the end of Q1-2018. Building on this consolidated installed base, the Company is targeting to grow its total installed base to around 250 to 300 analyzers by the end of 2018. Of these, a growing number is expected to be placed in the U.S. following the clearance of the Unyvero System and the Unyvero LRT Application Cartridge by the U.S. FDA in April 2018. Hence, Curetis USA Inc. within the next six to nine months targets the installation of around 40 to 50 Unyvero Analyzers across the U.S. and an increase to around 60 to 80 Analyzers within the first year following full commercial launch (i.e. Q2-2019).

         
Research & Development

  • To further advance its U.S. product portfolio, Curetis expects to initiate sites for prospective patient sample enrollment into its second U.S. FDA clinical trial for the Unyvero IJI Invasive Joint Infection Application Cartridge beginning in H2-2018, with the aim of completing this trial in 2019. Curetis will also in the coming months initiate a dialogue with the U.S. FDA on the data requirements for a label claim expansion of its current Unyvero LRT Cartridge to also include bronchoalveolar lavage (BAL) as a sample type and the potential expansion of its panel to include one further microorganism and certain additional resistance markers to further strengthen the clinical utility of this first-in-class application. Further U.S. FDA trials are expected to follow, subject to access to additional funding, thus continuing the portfolio expansion of available differentiated testing applications in the U.S.
     
  • The Company also anticipates that its Chinese partner Beijing Clear Biotech (BCB) is to complete all steps required by the Chinese regulatory agency CFDA in terms of analytical testing needed to initiate prospective clinical trials in China in the second half of 2018. The objective is to complete the first trials in 2019, with subsequent CFDA submission and approvals required for launch and commercialization in the Chinese market.
     
  • With the recent launch of the Unyvero UTI Application Cartridge for severe urinary tract infections, the Company has further expanded its offering of Unyvero A50 high-multiplex syndromic panels for hospital-acquired infections. The Company expects to further develop and expand its Unyvero A50 application portfolio through stringent life-cycle management of its existing applications as well as through development of selected novel applications.
     
  • In 2018, Curetis expects to work on further expanding the Unyvero platform beyond the core Unyvero A50 high-multiplex Analyzer and Unyvero A50 syndromic testing panels by advancing the development of the Unyvero A30 RQ Analyzer and additional application cartridges for this rapid, low- to mid-plex module to complement the Unyvero product offering as a broader platform in hospital infections. The Company expects to receive CE-IVD marking for the Unyvero A30 RQ Analyzer as well as first A30 RQ Application Cartridges during the course of 2019.

Business Development

  • Following the broad strategic Memorandum of Understanding (MoU) signed with MGI (a BGI Group company, China) in September 2017 and the further collaboration and commercialization agreements under this MoU signed in January 2018, Curetis expects first results and initial product launches from this collaboration in the 2018 and 2019 timeframe. Importantly, Curetis expects to continue to grow, broaden and deepen this strategic partnership with the BGI Group moving forward and to apply the Unyvero as well as Ares Genetics' bioinformatics competencies and assets to their NGS platform to fuel future growth. Curetis expects that the Companies will also explore further options for strategic and commercial collaborations in China and beyond.
     
  • Curetis also aims to enter into additional value-adding R&D and commercial partnerships with well-known players in the relevant industries that are based on the ARES AMR Database, ARESdb, and the ARES Technology Platform and/or the Unyvero A30 RQ Analyzer and further elements of the Unyvero Platform.

Financial Position and Financing

  • Building on stable year-over-year revenue in Q1-2018, a solid sales funnel in the EMEA region, the ongoing commercial launch in the U.S. and other developments described above, the Company aims to at least double its revenue year-over-year in 2018.
     
  • With the expansion of the U.S. commercial organization in December 2017 and Q1-2018 and the initiation of the U.S. commercial roll-out of the Unyvero System and the Unyvero LRT Application Cartridge as well as the continued development of the Unyvero A30 RQ Analyzer and further Unyvero Application Cartridges, in particular for the U.S. market (e.g. the Unyvero IJI Application Cartridge incl. clinical trials), the Company expects the net cash-burn from operating and investment activities for 2018 to be around 30 million EUR, an anticipated significant increase over cash burn of 15.7 million EUR in 2017.
     
  • Curetis will continue to assess all tactical and strategic financing options in the debt and equity capital markets globally. With the cash available at year-end 2017 (plus VAT receivable of EUR 0.3 million) in combination with up to EUR 15 million of additional debt financing from the EIB that may become available for draw-down by Curetis upon it meeting several agreed upon milestones (including an additional EUR 3 million EIB debt tranche which became available immediately upon the April 2018 FDA clearance), and the EUR 4.1 million from the recent private share placements and access to additional USD 10 million in equity mentioned above, Curetis aims to raise additional growth capital as either equity or debt in 2018 to secure appropriate funding and cash for continued operations for at least 12 months to ensure it has the financial resources to continue as a going concern. Depending on commercial success and financing availability, Curetis also expects to further grow its employee base at its various international sites and operations in the coming years.
     
  • Curetis also plans to pursue non-dilutive financing sources such as government grants or licensing and partnering models (e.g. for the Ares AMR Database and Unyvero A30 RQ Platform) to partially fund some of its operations in 2018 and 2019.

Full-Year 2017 Financial Results

For the twelve months ended December 31, 2017, revenues were EUR 1.2 million, as compared to revenues of EUR 1.3 million in 2016.

Gross loss for the year totaled EUR -462 thousand, compared with a gross loss of EUR -290 thousand in 2016, as under IFRS accounting the cost of goods for the Unyvero Application Cartridges still includes significant elements of as-yet unutilized capacity to allow for future expansion in manufacturing output. The full-year 2017 gross margin was -38.9%, compared with -22.2% for 2016.

Operating loss in 2017 totaled EUR -18.6 million, compared with EUR -15.2 million in 2016.

Net loss for the year was EUR -19.3 million compared with a net loss of EUR -15.2 million in 2016 due to expenses related to the commercial expansion, R&D and pipeline expansion efforts.

On December 31, 2017, Curetis Group's cash, cash equivalents and financial assets amounted to EUR 16.3 million (including the proceeds from an EIB loan facility drawn-down in April 2017 of EUR 10 million) compared with EUR 22.8 million as of December 31, 2016.

The financial statements 2017 have been prepared on a going concern basis despite the fact that as of December 31, 2017, remaining cash reserves were insufficient to cover at least 12 months after the signing date of the auditor's report. This determination was based on work conducted by the auditors PwC including detailed scenario analysis and risk assessments, incl. assessment of all strategic and tactical financing options with several additional cash inflows based on potential debt or equity financings and various cost reduction and cash preserving measures identified for implementation during 2018. Please also refer to Note 3.27 on 'Going Concern' of the Group's audited 2017 consolidated financial statements.

Earnings Conference Call and Webcast
Curetis will host a public earnings conference call and webcast today, April 30, 2018, at 03:00 pm CET / 09:00 am EST to discuss the financial results of 2017, highlight the most important events and provide an outlook for 2018 and beyond.

For participating in the earnings call conference please access the presentation at
https://webcasts.eqs.com/curetis20180430/no-audio

To access the call, please dial the following numbers using the passcode 93120684#

Belgium: +3211500307
Germany: +49 69 222229043
The Netherlands: +31107137273
UK: +44 20 30092452
US: +1 855 4027766

For further international dial-in numbers, please open the following link: http://events.arkadin.com/ev/docs/International%20Access%20Numbers_%20UKFELBRI1_SU7.pdf

The full annual financial report 2017 will be available as of today, April 30, 2018, at http://www.curetis.com/en/investors/financial-reports-and-conferences/financial-reports.html

The conference call will be supplemented by a presentation and a conference call webcast which can be accessed after completion of the call at http://www.curetis.com/en/investors/financial-reports-and-conferences/financial-reports.html

About Curetis
Curetis N.V.'s (Euronext: CURE) goal is to become a leading provider of innovative solutions for molecular microbiology diagnostics designed to address the global challenge of diagnosing severe infectious diseases and identifying antibiotic resistances in hospitalized patients.

Curetis' Unyvero System is a versatile, fast and highly automated molecular diagnostic platform for easy-to-use, cartridge-based solutions for the comprehensive and rapid detection of pathogens and antimicrobial resistance markers in a range of severe infectious disease indications. Results are available within hours, a process that can take days or even weeks if performed with standard diagnostic procedures, and thereby facilitates improved patient outcomes, stringent antibiotic stewardship and health economic benefits. Unyvero in vitro diagnostic (IVD) products are marketed in Europe, the Middle East, Asia and the U.S.

Curetis' wholly owned subsidiary Ares Genetics GmbH offers next-generation solutions for infectious disease diagnostics and therapeutics. The ARES Technology Platform combines the world's most comprehensive database on the genetics of antimicrobial resistances, ARESdb, with advanced bioinformatics and artificial intelligence.  

For further information, please visit www.curetis.com and www.ares-genetics.com.
Legal Disclaimer
This document constitutes neither an offer to buy nor an offer to subscribe for securities and neither this document nor any part of it should form the basis of any investment decision in Curetis.
The information contained in this press release has been carefully prepared. However, Curetis bears and assumes no liability of whatever kind for the correctness and completeness of the information provided herein. Curetis does not assume an obligation of whatever kind to update or correct information contained in this press release whether as a result of new information, future events or for other reasons.
This press release includes statements that are, or may be deemed to be, "forward-looking statements." These forward-looking statements can be identified by the use of forward-looking terminology, including the terms "believes," "estimates," "anticipates," "expects," "intends," "targets," "may," "will," or "should" and include statements Curetis makes concerning the intended results of its strategy. By their nature, forward-looking statements involve risks and uncertainties and readers are cautioned that any such forward-looking statements are not guarantees of future performance. Curetis' actual results may differ materially from those predicted by the forward-looking statements. Curetis undertakes no obligation to publicly update or revise forward-looking statements, except as may be required by law.

Contact details
Curetis
Max-Eyth-Str. 42
71088 Holzgerlingen, Germany
Tel. +49 7031 49195-10
pr@curetis.com or ir@curetis.com
www.curetis.com - www.unyvero.com

International Media & Investor Inquiries
akampion
Dr. Ludger Wess / Ines-Regina Buth
Managing Partners
info@akampion.com
Tel. +49 40 88 16 59 64
Tel. +49 30 23 63 27 68

U.S. Media & Investor Inquiries
The Ruth Group
Lee Roth
lroth@theruthgroup.com
Tel. +1 646 536 7012


CONSOLIDATED STATEMENT OF PROFIT OR LOSS AND OTHER COMPREHENSIVE INCOME

in kEuro 2017 2016
     
Revenue 1,187 1,306
Cost of sales -1,649 -1,596
Gross loss -462 -290
     
Distribution costs -7,302 -5,091
Administrative expenses -3,755 -3,024
Research & development expenses -7,362 -7,027
Other income 314 198
Operating loss -18,567 -15,234
     
Finance income 21 101
Finance costs -1,004 -30
Finance result -  net  -983 71
     
Loss before income tax -19,550 -15,163
Income tax expenses  52 -10
Loss for the period -19,498 -15,173
Other comprehensive income for the year, net of tax 171 -28
Total comprehensive income for the period -19,327 -15,201
     
Loss per share attributable to the ordinary equity holders of the company 2017 2016
Basic -1.26 -0.98
Diluted -1.26 -0.98


CONSOLIDATED STATEMENT OF FINANCIAL POSITION

Assets


in kEuro
  31 December 2017 31 December 2016
       
Current assets   24,009 30,272
  Cash and cash equivalents 16,311 22,832
  Trade receivables 200 101
  Inventories 6,946 5,870
  Other current assets 552 1,469
       
Non-current assets 11,506 12,514
  Intangible assets 7,524 7,520
  Property, plant and equipment 3,566 4,466
  Other non-current assets 182 212
  Other non-current financial assets 156 316
  Deferred tax assets 78 -
       
Total assets   35,515 42,786


CONSOLIDATED STATEMENT OF FINANCIAL POSITION

Liability & Equity

  in kEuro 31 December 2017 31 December 2016
       
Current liabilities 2,926 2,384
  Trade and other payables 928 721
  Provisions current 124 51
  Tax liabilities 24 10
  Other current liabilities 1,226 1,120
  Other current financial liabilities 624 482
       
Non-current liabilities 10,385 41
  Provisions non-current 43 41
  Other non-current financial liabilities 10,342 -
       
Total liabilities   13,311 2,425
       
Equity   22,204 40,361
  Share capital 155 155
  Capital reserve 152,793 152,793
  Other reserves 8,527 7,360
  Currency translation differences 143 -29
  Retained earnings -139,414 119,918
       
Total equity and liabilities 35,515 42,786


CONSOLIDATED STATEMENT OF CASH FLOWS

in kEuro    
  2017 2016
Profit before income tax -19,498 -15,172
Adjustment for:    
- Net finance income / costs 983 -71
- Depreciation, amortization and impairments 1,327 1,744
- Gain on disposal of fixed assets 2 2
- Changes in provisions 75 23
- Changes in equity settled stock options 1,167 767
- Changes in the PSOP-liability 0 -367
- Net exchange differences 371 -30
- Changes in deferred tax assets and liabilities -78 0
     
Changes in working capital relating to:    
- Inventories -1,076 -3,083
- Trade receivables and other receivables 1,008 201
- Trade payables and other payables 911 270
     
Effects of exchange rate differences not realized from consolidation -199 2
Income taxes received (+) / paid (-) -52 0
Interest paid (-) -622 -10
Net cash flow provided by operating activities -15,681 -15,724
Payments for intangible assets -111 -7,025
Payments for property, plant and equipment -320 -456
Interest received 10 51
Net cash flow used in investing activities -421 -7,430
Proceeds from other non-current financial liabilities 10,000 0
Payments for finance lease liabilities -48 -105
Net cash flow provided by financing activities 9,952 -105
     
Net increase in cash and cash equivalents -6,150 -23,259
Net cash and cash equivalents at the beginning of the year 22,832 46,060
Net decrease in cash and cash equivalents -6,150 -23,258
Effects of exchange rate changes on cash and cash equivalents -371 30
Net Cash and cash equivalents at the end of the period 16,311 22,832



[1] as previously announced on February 5, 2018




This announcement is distributed by Nasdaq Corporate Solutions on behalf of Nasdaq Corporate Solutions clients.
The issuer of this announcement warrants that they are solely responsible for the content, accuracy and originality of the information contained therein.
Source: Curetis via Globenewswire

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Curetis
Max-Eyth-Str. 42 Holzgerlingen Germany
 
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