Market Overview

Onxeo Reports Half-Year 2018 Financial Results and Provides Business Outlook

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  • Clinical development of Onxeo's lead product candidate AsiDNA™
    progressing to plan
    • Preliminary safety and activity results of DRIIV-1 study are
      expected in Q4 2018
    • Two combination clinical trials with AsiDNA™ planned for early
      2019
  • New optimized candidate from platON™ proprietary platform ready to
    enter preclinical stage by end 2018
  • Cash position of €11m at June 30, 2018 enables an expanded clinical
    development plan of AsiDNA™ into 2020

Regulatory News:

Onxeo S.A. (Euronext Paris, NASDAQ Copenhagen: ONXEO
FR0010095596), a clinical-stage biotechnology company specializing in
the development of innovative drugs in oncology, in particular against
rare or resistant cancers, today reported its consolidated half-year
financial results1, as of June 30, 2018 and provided a
business update.

Judith Greciet, Chief Executive Officer of Onxeo, said: "The
first half of 2018 was marked by an important step in the development of
our lead product candidate AsiDNA™ as it entered a phase I clinical
trial DRIIV-1 in patients with advanced solid tumors. We expect
preliminary data in Q4 2018 which will confirm both the safety and
systemic activity of this first-in-class DNA repair inhibitor. In
parallel, we have conducted substantial preclinical work with AsiDNA™ in
combination with other anticancer agents to assess its full potential.
In that context, we have already obtained very compelling data regarding
the synergistic effects and reversion of tumor resistance by AsiDNA™
when combined with a PARP inhibitor. Additional results on the interest
of combining AsiDNA™ with belinostat have also been acquired and other
experiments are ongoing to show the value of combining AsiDNA™ with
carboplatin, a standard-of-care in chemotherapy. Together with the
expected outcomes from the DRIIV-1 clinical study, this solid body of
preclinical data opens a range of new clinical development opportunities
to harvest the full potential of AsiDNA™ and we have planned already to
broaden its development in combination as soon as 2019.

"Furthermore, the extensive screening and optimization work on new
molecules sourced from our PlatON™ platform is bearing fruit and we
expect to advance the next optimized candidate into preclinical
development by the end of the year, thereby enlarging Onxeo's pipeline.

"At this time and considering our available preclinical data, it
appears that AsiDNA™ in combination with PARPi and/or carboplatin is the
most promising option while belinostat could be best combined with a new
candidate sourced from platON™, due to the respective pharmacokinetic
properties of these assets.

"During this half-year, we also strengthened our cash position with
an equity line and the monetization of Beleodaq® royalties, to support
the momentum of our development programs with this highly attractive
technology in DNA targeting."

1 Half-year financial statements have been the subject of a
limited review. The limited review report will be issued after the
procedures required for the publication of the half-yearly financial
report have been finalized.

HALF-YEAR 2018 FINANCIAL RESULTS

Revenues for the first half of 2018 stood at €2.1 million and
consisted of:

  • €1.2 million in recurring revenues, corresponding to product sales
    from the European named patient program (NPP) and sales-based
    royalties related to the license agreements with Spectrum
    Pharmaceuticals. The decrease compared to 2017 mainly comes from the
    sale of the Loramyc® and Sitavig products to Vectans Pharma at the end
    of July 2017.
  • €0.9 million in non-recurring revenues including mainly milestone
    payments from a licensing agreement. The implementation of the new
    IFRS15 standards on revenue recognition as of January 1, 2018,
    negatively impacted Onxeo's non-recurring revenue by approximately
    €0.5 million in the first half of 2018.

Operating expenses amounted to €7.6 million in H1 2018, which
represented a decrease of 48% compared to H1 2017 which was essentially
due to cost reduction following the interruption of the Livatag® program.

The Company also booked a €4 million operational income corresponding to
the write-off of a cash advance from Bpifrance relating to the Livatag®
program, for which the objective of commercial success was not achieved.

On July 27, 2018, the board of directors reviewed the Company's
consolidated accounts for the first-half of 2018 and recorded an
impairment charge of €8.6 million pursuant to value tests performed in
accordance with IFRS accounting standards. This accounting adjustment
results from a potential better synergy between belinostat and a future
compound from platON™ versus a development with AsiDNA™, thereby
postponing cumulative future cash flows on this product. This does not
impact in any way the Company's current or future cash balance or its
ability to advance its strategic value creation strategy as planned. The
impairment triggered a reduction of the Company's deferred tax liability
by €1.7 million, recognized as a profit.

H1 2018 total net loss was of €8.8 million, compared to €11.6
million in H1 2017.

         
Consolidated income statement (IFRS)

In thousands of euros

  30/06/2018

(6 months)

  30/06/2017

(6 months)

Revenues, of which:

    Recurring revenues

    Non-recurring revenues

  2,102

1,040

1 062

  3,367

1,893

1,474

Operating expenses, of which

    R&D expenses (net of R&D tax credit)

  (7,578)

(3,187)

  (14,674)

(10,481)

Operating income/(loss) before non-recurring items   (5,476)   (11,307)

Non-recurring operating income/(loss), of which

    impairment of R&D assets related to Beleodaq®

  (4,627)

(8,549)

  (17)

-

Financial income/(loss)   (444)   (338)
Income tax   1,711   35
Net profit/(loss)   (8,836)   (11,627)

CASH POSITION AT JUNE 30, 2018

At June 30, 2018, the Company had a consolidated cash position of €11
million compared with €14.3 million at December 31, 2017, providing
visibility until Q1 2020, based on the current financing plan that
includes an expanded development for AsiDNA™.

Cash variation takes into account the $7.5 million (net proceed of
€6.1m) of non-dilutive capital from SWK Holdings Corporation through the
sale of rights related to future Beleodaq® royalties on June 7, 2018. In
order to actively pursue its R&D programs, Onxeo also implemented, on
June 15, 2018, an equity financing line including an incentive program
through the issuance of new shares over a 10-month period representing a
maximum amount of €5.4 million with Nice & Green SA, included in the
financing plan.

HALF-YEAR 2018 CORPORATE HIGHLIGHTS, RECENT EVENTS & OUTLOOK

  • AsiDNA™
    • Onxeo obtained a new ‘composition of matter' patent in Europe in
      January 2018 covering multiple compounds, including AsiDNA™, and
      providing protection until 2031 with a potential extension to
      2036. Together with previously granted patents, Onxeo's
      intellectual property for its DNA-targeting technologies, products
      and combinations is now protected by 10 patent families worldwide.
    • The Company also initiated, end of April 2018, a dose-escalation
      phase I study (DRIIV-1) with AsiDNA™ to assess the compound's
      safety profile and identify its optimal clinical dose, as well as
      determine its active dose at tumor level, in patients with
      advanced solid cancer. Preliminary results are expected in Q4 2018.
    • New preclinical results of AsiDNA™ in combination with PARP
      inhibitors, announced in July 2018, showed a strong synergistic
      effect and a reversion of tumor resistance, thereby confirming the
      relevance of combining AsiDNA™ with PARP inhibitors. These
      positive in vitro and in vivo data, together with
      the expected activity results of the DRIIV-1 study, will support
      further clinical development of AsiDNA™ in combination with PARP
      inhibitors, which should start from end 2018. Results from
      preclinical studies of other combinations will be available after
      the summer.

These results comfort AsiDNA™ as the Company's priority development
program.

  • platON™
    • Onxeo's patented chemistry platform enables the Company to
      generate additional innovative DNA-targeting drug candidates.
    • Several compounds are currently in the selection and optimization
      phase and Onxeo expects to initiate the preclinical evaluation of
      a new drug candidate by the end of 2018.
  • Belinostat
    • Preclinical data obtained in combination with AsiDNA™ were
      presented to the scientific community during one of the two poster
      presentations at AACR 2018.
  • Corporate governance
    • On May 16, 2018, the shareholders' Ordinary General Meeting
      renewed for three years the terms of office as director of Mr.
      Thomas Hofstaetter, President of Onxeo's Compensation and
      Scientific & Business Development committees.

UPCOMING FINANCIAL PUBLICATIONS & EVENTS

  • Q3 2018 financial information: Thursday, October 25, 2018,
    after market

About Onxeo

Onxeo (Euronext Paris, NASDAQ Copenhagen: ONXEO) is a French
biotechnology company developing innovative oncology drugs based on
DNA-targeting and epigenetics, two of the most sought-after mechanisms
of action in cancer treatment today. The Company is focused on bringing
early-stage first-in-class or disruptive compounds (proprietary,
acquired or in-licensed) from translational research to clinical
proof-of-concept, a value-creating inflection point appealing to
potential partners.

Onxeo is developing AsiDNA™, a first-in-class DNA break repair
inhibitor based on a unique decoy mechanism. AsiDNA™ has already
successfully completed a Phase I trial in metastatic melanoma via local
administration and is currently being evaluated for systemic (IV)
administration in solid tumors in the DRIIV-1 phase I study (DNA Repair
Inhibitor administered IntraVenously).

AsiDNA™ is the first compound generated from platON™, the
Company's proprietary chemistry platform of decoy oligonucleotides based
on three components, a sequence of double strand oligonucleotides, a
linker and a cellular uptake facilitator. PlatON™ will continue to
generate innovative compounds targeting tumor DNA functions and broaden
Onxeo's pipeline.

Onxeo's R&D pipeline also includes belinostat, an HDAC
inhibitor (epigenetics), of which an oral form could be used in
combination with other anti-cancer agents for liquid or solid tumors.
Belinostat is already conditionally FDA-approved in the US as a 2nd
line treatment for patients with peripheral T cell lymphoma and marketed
in the US by Onxeo's partner, Spectrum Pharmaceuticals, under the name
Beleodaq® (belinostat IV form).

For further information, please visit www.onxeo.com.

Forward looking statements

This communication expressly or implicitly contains certain
forward-looking statements concerning Onxeo and its business. Such
statements involve certain known and unknown risks, uncertainties and
other factors, which could cause the actual results, financial
condition, performance or achievements of Onxeo to be materially
different from any future results, performance or achievements expressed
or implied by such forward-looking statements. Onxeo is providing this
communication as of this date and does not undertake to update any
forward-looking statements contained herein as a result of new
information, future events or otherwise. For a discussion of risks and
uncertainties which could cause actual results, financial condition,
performance or achievements of Onxeo to differ from those contained in
the forward-looking statements, please refer to the section 5.7.1.4
"Risk Factors" ("Facteurs de Risque") of the 2017
registration document filed with the Autorité des marchés financiers
on April 25, 2018 under number D.18-0389, which is available on the Autorité
des marchés financiers
website (www.amf-france.org)
or on the Company's website (www.onxeo.com).

APPENDICES - HALF-YEARLY CONSOLIDATED ACCOUNTS AT JUNE 30, 2018

The 2018 half-yearly financial report will be available on the Company's
website within the prescribed deadlines.

CONSOLIDATED STATEMENT OF FINANCIAL POSITION

         
ASSETS in K€   30/06/2018   31/12/2017
   
Non-current assets
Intangible assets 38,734 47,535
Tangible assets 275 344
Financial assets   244   232
Total non-current assets   39,253   48,111
 
Current assets
Stock and work-in-progress 33 30
Trade receivables 1,483 552
Other receivables 6,519 15,103
Cash 11,014 14,277
Total current assets 19,049 29,962
         
TOTAL ASSETS   58,302   78,073
 
         
LIABILITIES AND SHAREHOLDERS' EQUITY K€   30/06/2018   31/12/2017
Shareholders' equity
Share capital 12,684 12,674
Less: treasury shares -96 -89
Premium 39,892 269,060
Reserves -1,395 -172,700
Earnings   - 8,836   -59,071
Total shareholders' equity   42,248   49,873
 
Non-current liabilities
Deferred tax liabilities 2,366 4,094
Provisions 546 550
Other financial liabilities   7,067   4,714
Total non-current liabilities   9,979   9,358
 
Current liabilities
Short-term financial debt 101 130
Trade payables and related accounts 4,330 5,956
Other liabilities   1,644   12,755
Total current liabilities   6,075   18,842
         
TOTAL LIABILITIES AND SHAREHOLDERS' EQUITY   58,302   78,073

CONSOLIDATED STATEMENT OF COMPREHENSIVE INCOME

         
In K€   30/06/2018   30/06/2017
   
 
Recurrent sales from licensing agreement 1,040 1,893
Non-current sales from licensing agreement   1,062   1,474
Total sales   2,102   3,367
Purchases -211 -415
Personnel costs -2,682 -,3,716
External expenses -4,228 -,9,672
Duties and taxes -196 -179
Depreciation and amortization, net -311 -900
Allowances to provisions, net 163 969
Other operating income 3
Other operating expenses   -114   -765
Operating expenses   -7,578   -14,674
Current operating income   -5,476   -11,307
Share of income under the equity method -17
Other operational income 4,036
Other operational expenses   -8,663    
Operating income after share of income under the equity method   -10,103   -11,324
Income from cash and cash equivalents 530
Other financial income 87 16
Financial expenses   -532   -884
Financial income   -444   -338
Pre-tax income   -10,547   -11,663
Income tax 1,711 35
-of which deferred tax   1,728   0
Net profit/loss   -8,836   -11,627
Earnings per share -0,17 -0,23
Diluted earnings per share   -0,17   -0,23

OTHER ELEMENTS OF THE STATEMENT OF COMPREHENSIVE INCOME

         
In K€   30/06/2018   30/06/2017
Income for the period   -8,836   -11,627
Other comprehensive income    
Translation adjustments 2,201 955
Losses and gains on derecognition of assets available for sale
Cash flow hedges
Tax related to elements of the comprehensive income
Other items recycled as income 2 201 955
Actuarial gains and losses 0 -21
Other non-recyclable items classified as income   0   -21
Other elements of the comprehensive income for the period net of
taxes
  2,201   934
Total comprehensive income for the period   -6,635   -10,693
Total comprehensive income attributable to :

- Owners of the parent company

- Minority interests

  -6,635   -10,593

CONSOLIDATED NET CASH FLOW STATEMENT

             
In K€   30/06/2018   31/12/2017   30/06/2017
Consolidated net loss   -8,836   -59,071   -11,627
+/- Depreciation, impairment and provisions, net   8,888   40,253   949
(excluding provisions against working capital)
-/+ Unrealized gains and losses associated with changes in fair value 432
+/- Non-cash income and expenses on stock options and similar items 311 980 249
-/+ Other calculated income and expenses -67 -137 -92
-/+ Capital gains and losses on disposal
-/+ Dilution gains and losses
+/- Share of earning associates 0 0 17
- Dividends (non-consolidated equity)
Gross operating cash flow after net cost of debt and tax 728 -17,973 -10,504
+ Cost of financial debt, net 12 492 338
+/- Tax liabilities (including deferred tax) -1,728 -7,801 35
Gross operating cash flow before net cost of debt and tax -988 -25,282 -10,130
- Taxes paid
+/- Changes in operating WCR (including debt related to employee
benefits)
  -8,631   -2,999   -5,547
NET CASH FLOW FROM OPERATING ACTIVITES   -9,620   -28,281   -15,677
- Expenditures on acquisition of tangible and intangible assets -17 -65 -25
+ Proceeds of disposals of tangible and intangible assets 2
- Expenditures on acquisition of financial assets (non-consolidated
equity)
12 -2 -2
+ Proceeds of disposals of financial assets (non-consolidated equity) 2
+/- Impact of perimeter variations
+ Dividends received (non-consolidated equity, associated companies)
+/- Changes in agreed upon loans and advances
+ Investment grants received
+/- Other cash flow from investment activities            
NET CASH FLOW FROM OPERATING ACTIVITIES   -5   -67   -23
Cash flow from merger
+ Amounts received from shareholders at capital increases
. From parent company shareholders 48 14,012 14,702
. From minority interest of merged entity
+ Amounts received from stock options
-/+ Buy-back and resale of treasury shares -1 -68 -1
- Dividends paid during period
. To shareholders of parent company
. To minority interests of merged entity
+ Proceeds of new loans 6,375
- Reimbursement of loans (including finance leases) -77 -154 -320
- Net interests paid (including finance leases)
+/- Other flows related to financing activities   -12   -354   -229
NET CASH FLOW FROM FINANCING ACTIVITIES   6,333   13,437   14,155
+/- Impact of fluctuations in foreign exchange rates   29   -55   -44
CHANGES IN CAHS AND CASH EQUIVALENTS   -3,263   -14,966   -1,590
CASH AND CASH EQUIVALENTS at start of period   14,277   27,654   29,243
CASH AND CASH EQUIVALENTS at end of period   11,014   14,277   27,654

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