12.04.2018
Heidelberg Pharma AG DE000A11QVV0
DGAP-News: Heidelberg Pharma AG: Interim Management Statement on the First Three Months of 2018
DGAP-News: Heidelberg Pharma AG / Key word(s): Interim Report
Heidelberg Pharma AG: Interim Management Statement on the First Three Months
of 2018
12.04.2018 / 07:03
The issuer is solely responsible for the content of this announcement.
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Heidelberg Pharma AG: Interim Management Statement on the First Three Months
of 2018
- Exclusive research agreement signed with Magenta for the development of
Antibody Targeted Amanitin Conjugates
- License agreement signed with the University of Texas MD Anderson Cancer
Center
- Outlook for 2018: increase investments in proprietary ATAC pipeline for
the preparation of the clinical development
Ladenburg, Germany, 12 April 2018 - Heidelberg Pharma AG (FSE: WL6) today
reported on the first three months of fiscal year 2018 (1 December 2017 - 28
February 2018) and the Group's financial figures.
Important operational achievements
- License agreement with the University of Texas MD Anderson Cancer Center:
At the beginning of March 2018, Heidelberg Pharma Research GmbH as the
licensee and The University of Texas System, Houston, TX, USA, signed a
license agreement for patent rights related to the diagnosis and treatment
of patients with so-called RNA polymerase II deletion. The subject of the
license is a patent application, filed in the name of the Board of Regents
of The University of Texas System, which covers important aspects of a
potential personalized treatment of patients based on Heidelberg Pharma's
ATAC technology (Antibody Targeted Amanitin Conjugates).
- Exclusive research agreement with Magenta for the development of Antibody
Targeted Amanitin Conjugates: On 5 March 2018, Heidelberg Pharma announced
that it had signed an exclusive multi-target research agreement with Magenta
Therapeutics, Cambridge, MA, USA, (Magenta). The collaboration will combine
Magenta's stem cell platform with proprietary antibodies for up to four
exclusive targets with Heidelberg Pharma's proprietary ATAC technology for
the development of new Antibody Targeted Amanitin Conjugates. Magenta is
granted access to Heidelberg Pharma's Amanitin linker platform technology,
and it has an option for an exclusive license for global development and
commercialization rights to each of the product candidates resulting from
the collaboration.
As licensor, Heidelberg Pharma receives upfront technology access and
exclusivity fees and payments for research support. Under the exclusive
license agreement, Heidelberg Pharma would be eligible to receive clinical
development, regulatory and sales-related milestone payments of up to USD
334 million, if Magenta were to exercise the options on all target molecules
and all milestones were reached.
Results of operations, financial position and net assets
The Heidelberg Pharma Group - as of the reporting date comprising Heidelberg
Pharma AG and subsidiary Heidelberg Pharma Research GmbH - reports
consolidated figures. The reporting period referred to below concerns the
period from 1 December 2017 to 28 February 2018 (first quarter 2018).
In the first three months of fiscal year 2018, the Group generated sales
revenue and income totaling EUR 0.7 million (previous year: EUR 0.6
million). This figure includes sales revenue of EUR 0.6 million (previous
year: EUR 0.5 million), which stems solely from the business of Heidelberg
Pharma Research GmbH. Income from the research agreement with Magenta is not
included, as the agreement was signed in March after the reporting period.
At EUR 0.1 million, other income remained at the previous year's level (EUR
0.1 million). It primarily consists of German and European grants and of the
reversal of unutilized accrued liabilities and provisions.
Operating expenses including depreciation and amortization amounted to EUR
3.1 million in the reporting period (previous year: EUR 2.5 million). Cost
of sales for customer-specific research amounted to EUR 0.4 million
(previous year: EUR 0.2 million). Research and development (R&D) costs of
EUR 2.1 million were up EUR 0.5 million compared to the prior-year period
(EUR 1.6 million) due to an increase in costs related to preparations for
external GMP production (Good Manufacturing Practice) incurred by Heidelberg
Pharma Research GmbH. At 66% of operating expenses, R&D was by far the
largest cost item as expected. Administrative costs in the first quarter of
2018 remained constant at EUR 0.6 million compared to the prior-year period.
Among others, this figure includes holding company costs and costs related
to the stock market listing. Other expenses for business development,
marketing and commercial market supply activities amount to EUR 0.03 million
in the current reporting period (previous year: EUR 0.05 million).
The Heidelberg Pharma Group's net loss for the first three months of the
fiscal year increased to EUR 2.4 million, as planned (previous year: EUR 2.0
million).
In spite of the higher net loss, earnings per share improved from EUR -0.15
in the previous year to EUR -0.11 in the quarter just ended, due to the
higher average number of shares.
Total assets as of 28 February 2018 amounted to EUR 38.1 million compared to
the 30 November 2017 reporting date (EUR 41.5 million) due to a decrease in
cash and cash equivalents. At EUR 34.6 million, equity was also down
compared to the end of fiscal year 2017 (EUR 37.0 million). This corresponds
to an equity ratio of 91.0% (30 November 2017: 89.2%). The exercise of
convertible bonds (mandatory convertible bonds) resulted in 5,649,964 new no
par value shares that increased the share capital of Heidelberg Pharma AG
from EUR 22,452,570 to EUR 28,102,534 divided into 28,102,534 no par value
bearer shares.
No corporate actions were implemented during the reporting period.
Cash and cash equivalents as of the end of the first quarter amounted to EUR
27.2 million (30 November 2017: EUR 30.4 million). This represents an
average monthly cash outflow of EUR 1.08 million in the first quarter of the
fiscal year (previous year: EUR 0.67 million).
Financial outlook for 2018
Financial guidance remains unchanged compared to that provided on 22 March
2018. The Heidelberg Pharma Group expects to generate between EUR 3.0
million and EUR 5.0 million in sales revenue and other income (2017: EUR 2.5
million) for the 2018 fiscal year. This guidance takes into account
potential cash inflows from new licensing activities. According to current
plans, operating expenses should be in the range of EUR 16.0 million to EUR
20.0 million (2017: EUR 13.2 million). Earnings before interest and taxes
(EBIT) for the 2018 fiscal year are projected to be between EUR -12.0
million and EUR -16.0 million (2017: EUR -10.8 million).
Heidelberg Pharma expects to require funds of EUR 13.0 million to EUR 17.0
million in 2018. Monthly cash use should be in the range of EUR 1.1 million
to EUR 1.4 million. Based on current planning, the Company's financing is
secured into 2020.
Heidelberg Pharma will not hold a conference call on this interim management
statement. The complete figures for the interim financial statement can be
downloaded at www.heidelberg-pharma.com > Press+Investors > Announcements >
Financial Reports > Interim Management Statement of 12 April 2018.
Key figures for the Heidelberg Pharma Group
In EUR'000 Q1 2018 1 Q1 2017 1 EUR
EUR'000. '000.
Earnings
Sales revenue 592 455
Other income 124 134
Operating expenses (3,130) (2,498)
of which research and development (2,075) (1,634)
costs
Operating result (2,414) (1,909)
Earnings before tax (2,414) (1,965)
Net loss for the period (2,414) (1,965)
Earnings per share in EUR (0.11) (0.15)
Balance sheet as of the end of the
period
Total assets 38,064 13,304
Cash and cash equivalents 27,151 2,568
Equity 34,641 7,823
Equity ratio2 in % 91.0 58.8
Cash flow statement
Cash flow from operating activities (3,087) (1,904)
Cash flow from investing activities (154) (104)
Cash flow from financing activities 0 0
Employees (number) 60 53
Employees as of the end of the 54 49
period3
Full-time equivalents as of the end
of the period3
1 The reporting period begins on 1 December and ends on 28 February.
2 Equity / total assets
3 Including members of the Executive Management Board
Rounding of exact figures may result in differences.
Contact Heidelberg Pharma AG IR/PR support MC Services AG
Corporate Communications Sylvia Katja Arnold (CIRO) Managing
Wimmer Tel.: +49 89 41 31 38-29 Director & Partner Tel.: +49 89
Email: investors[at]hdpharma.com 210 228-40 Cell: +49 160 9360
Schriesheimer Str. 101, 68526 3022 Email:
Ladenburg Germany katja.arnold[at]mc-services.eu
About Heidelberg Pharma
Heidelberg Pharma AG is a biopharmaceutical company based in Ladenburg,
Germany. Heidelberg Pharma is an oncology specialist and the first company
to develop the toxin Amanitin into cancer therapies using its proprietary
Antibody Targeted Amanitin Conjugate (ATAC) technology and to advance the
biological mode of action of the toxin as a novel therapeutic principle.
This proprietary technology platform is being applied to develop the
Company's proprietary therapeutic ATACs as well as in third-party
collaborations to create a variety of ATAC candidates. The proprietary lead
candidate HDP-101 is a BCMA ATAC for multiple myeloma.
The Company has entered into partnerships to further develop and
commercialize its clinical assets MESUPRON(R) and REDECTANE(R), while
RENCAREX(R) is available for out-licensing and further development.
Heidelberg Pharma AG is listed on the Frankfurt Stock Exchange: ISIN
DE000A11QVV0 / WKN A11QVV / Symbol WL6. More information is available at
http://www.heidelberg-pharma.com/.
This communication contains certain forward-looking statements relating to
the Company's business, which can be identified by the use of
forward-looking terminology such as "estimates", "believes", "expects",
"may", "will", "should", "future", "potential" or similar expressions or by
a general discussion of the Company's strategy, plans or intentions. Such
forward-looking statements involve known and unknown risks, uncertainties
and other factors, which may cause our actual results of operations,
financial position, earnings, achievements, or industry results, to be
materially different from any future results, earnings or achievements
expressed or implied by such forward-looking statements. Given these
uncertainties, prospective investors and partners are cautioned not to place
undue reliance on such forward-looking statements. We disclaim any
obligation to update any such forward-looking statements to reflect future
events or developments.
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12.04.2018 Dissemination of a Corporate News, transmitted by DGAP - a
service of EQS Group AG.
The issuer is solely responsible for the content of this announcement.
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Language: English
Company: Heidelberg Pharma AG
Schriesheimer Str. 101
68526 Ladenburg
Germany
Phone: +49 (0)89 41 31 38 - 0
Fax: +49 (0)89 41 31 38 - 99
E-mail: [email protected]
Internet: www.heidelberg-pharma.com
ISIN: DE000A11QVV0
WKN: A11QVV
Listed: Regulated Market in Frankfurt (Prime Standard); Regulated
Unofficial Market in Berlin, Dusseldorf, Munich,
Stuttgart, Tradegate Exchange
End of News DGAP News Service
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