AI Terminal

MODULE: AI_ANALYST
Interactive Q&A, Risk Assessment, Summarization
MODULE: DATA_EXTRACT
Excel Export, XBRL Parsing, Table Digitization
MODULE: PEER_COMP
Sector Benchmarking, Sentiment Analysis
SYSTEM ACCESS LOCKED
Authenticate / Register Log In

Apontis Pharma AG

Investor Presentation Aug 11, 2022

725_ip_2022-08-11_42e5c3d3-a647-4806-9d96-d815e32b8077.pdf

Investor Presentation

Open in Viewer

Opens in native device viewer

APONTIS PHARMA

The Single Pill Company

H1 2022 Results

Disclaimer

The following presentation, including any printed or electronic copy of these slides, the talks given by the presenters, the information communicated during any delivery of the presentation and any question and answer session and any document or material distributed at or in connection with the presentation (together, the "Presentation"), has been prepared by APONTIS PHARMA AG (the "Company"), is not an offer to sell any securities or an invitation to purchase securities or the solicitation of an offer to buy securities. This Presentation is not an advertisement and not a prospectus for the purposes of Regulation (EU) 2017/1129 of the European Parliament and of the Council of June 14, 2017, as amended.

The Presentation is provided for general information only and does not purport to contain all the information that may be required to evaluate the Company. The information in the Presentation is subject to updating, completion, revision and verification.

No reliance may be placed for any purpose whatsoever on the information or opinions contained or expressed in the Presentation or on the accuracy, completeness or fairness of such information and opinions. To the extent permitted by law and regulation, no undertaking, representation or warranty or other assurance, express or implied, is made or given by or on behalf of the Company, or any of its parent or subsidiary undertakings or the subsidiary undertakings of any such parent undertakings or any of its respective directors, officers, partners, employees, agents, affiliates, representatives or advisers, or any other person, as to the accuracy, completeness or fairness of the information or opinions contained in the Presentation.

None of the Company, its affiliates and advisers, agents and/or any other party undertakes or is under any duty to update the Presentation or to correct any inaccuracies in any such information which may become apparent or to provide you with any additional information. Save in the case of fraud, no responsibility or liability is accepted by any such person for any errors, omissions or inaccuracies in such information or opinions or for any loss, cost or damage suffered or incurred, however arising, directly or indirectly, from any use of, as a result of the reliance on, or otherwise in connection with, the Presentation. In addition, no duty of care or otherwise is owed by any such person to recipients of the Presentation or any other person in relation to the Presentation.

The Presentation includes statements that are, or may be deemed to be, forward-looking statements. These statements are based on the current views, expectations and assumptions of the management of the Company and involve known and unknown risks and uncertainties that could cause actual results, performance or events to differ materially from those expressed or implied in such statements. Actual results, performance or events may differ materially from those described in such statements due to, among other things, changes in the general economic and competitive environment, risks associated with capital markets, currency exchange rate fluctuations and competition from other companies, changes in international and national laws and regulations, in particular with respect to tax laws and regulations, affecting the Company and other factors. The Company does not assume any obligations to update any forwardlooking statements. The Presentation includes statistics, data and other information relating to markets, market sizes, market shares, market positions and other industry data pertaining to the Company's business and markets. Unless otherwise indicated, such information is based on analysis by the Company of multiple sources, including certain studies commissioned from third parties (the "Market Reports"). The Market Reports may include and be based on, amongst other things, information obtained from primary interviews and field visits conducted by third parties with industry experts and participants, third parties' secondary market research and internal financial and operational information supplied by, or on behalf of, the Company, as well as information obtained from (i) data providers; (ii) industry associations and country organizations; and (iii) publicly available information from other sources, such as information publicly released by the Company's competitors. To the extent available, the industry, market and competitive position data contained in the Presentation has come from official or third-party sources. Third-party industry publications, studies and surveys generally state that the data contained in them have been obtained from sources believed to be reliable, but that there is no guarantee of the accuracy or completeness of such data. While the Company believes that each of these publications, studies and surveys has been prepared by a reputable source, the Company has not independently verified the data contained therein. In addition, certain of the industry, market and competitive position data contained in the Presentation come from the Company's own internal research and estimates based on the knowledge and experience of the Company's management in the markets in which the Company operates. While the Company believes that such research and estimates are reasonable and reliable, they, and their underlying methodology and assumptions, have not been verified by any independent source for accuracy or completeness and are subject to change without notice. Accordingly, undue reliance should not be placed on any of the industry, market or competitive position data contained in the Presentation. All projections, valuations and statistical analyses are provided to assist the recipient in the evaluation of the matters described in the Presentation. They may be based on subjective assessments and assumptions and may use one among alternative methodologies that produce different results and, to the extent that they are based on historical information, they should not be relied upon as an accurate prediction of future performance.

The distribution of this Presentation in certain jurisdictions is restricted by law. Therefore, it must not be distributed, published or reproduced (in whole or in part) or disclosed by its recipients to any other person for any purpose, other than with the consent of the Company. All trademarks remain the property of their respective owners. By accepting receipt of, attending any delivery of, or electronically accessing, the Presentation, you agree to be bound by the above limitations and conditions and, in particular, you represent, warrant and undertake to the Company that: (i) you will not forward the Presentation to any other person or reproduce or publish this document, in whole or in part, for any purpose; and (ii) you have read and agree to comply with the contents of this notice.

APONTIS PHARMA Executive Team

Thomas Milz

Chief Product Officer

  • Business Development
  • Market Access
  • Medical & Regulatory Affairs
  • Product Development

Karlheinz Gast

Chief Executive Officer

  • Strategy
  • Marketing & Sales
  • Human Resources
  • Investor Relations

Thomas Zimmermann

Chief Finance Officer

  • Finance
  • Supply Chain
  • IT
  • Compliance

"Drug non-compliance is a stealth epidemic exacting a heavy toll on the healthcare system – our broad portfolio of Single Pills is designed to help tackle this epidemic"

APONTIS PHARMA with successful first half-year 2022

Financial Highlights H1 2022

Successful H1 2022 strengthens financial position

APONTIS PHARMA with successful first half-year 2022

New Single Pill launches, pipeline progress and extended cooperation

Launch Marketing Marketing Development Development Co-Promotion Divesture
of authorization authorization agreement agreement agreement of
Tonotec
Lipid
granted application with with with gynecology
and for submitted Develco Midas AstraZeneca products
for for for prolonged (legacy)
AmloAtor RosuASS Caramlo
HCT
2 Single Pills 2 Single Pills 2023

Further expansion of our Single Pill portfolio

APONTIS PHARMA with successful first half-year 2022

Business Execution

Full publications Expansion 7.770 physicians +10 sales reps Limited physician
of of promotional trained to support access
START-study activities to on Single Pills related to
in rehabilitation START-study and additional
peer-reviewed hospitals Single Pill AstraZeneca COVID-19-work,
journals treatment co-operation e.g., vaccination

Further expansion of our Single Pill portfolio

APONTIS PHARMA: Dynamic continuation of growth course

Key performance indicators H1 2022

(in EUR million)

Revenues

  • Single Pills +27%
  • Co-Marketing +2%
  • Others +19% (influenced by the selling of the Gyn products)

Gross Profit

Decline in gross profit margin impacted by Ulunar (Novartis): contract changed from Co-marketing to distribution model. Changed treatment of post-milestone payments in 2022 (impact EURm 0.5).

EBITDA/Net Result

  • Higher sales in H1 compared to previous period and IPO costs of EURm 3.5 last year main driver of profitability increase.
  • Gross profit impact related to changed Co-Marketing contract
  • Income from divestment of Gyn products in the amount of approx. EUR 0.6 Mio.
  • Repayment of shareholder loan in 2021: EUR 0.4 Mio lower interest expense.

Momentum for Single Pills continues

  • Growth in Single Pills driven in particular by Atorimib, Tonotec, Tonotec HCT and LosAmlo
  • 4 out of 7 single pills with high double-digit growth
  • Two new Single Pills launched
  • Caramlo below prior year due to tender and high wholesaler stockpiling in December 2021 (EURk 500)
  • Growth in co-marketing/co-promotion driven by Copromotion of AstraZeneca's product Trixeo
  • Ulunar sales declined with 12% lower than expected
  • Jalra/Icandra at prior year level due to supply constraints at Novartis
  • Others benefit from
  • Normal cough season after COVID-19 restrictions fall end of Q1 2021
  • Sale of complete inventories with divestment of gynecology business

Note: Rounding differences may occur. Source: Company data

Solid Financial Position: Well-Funded for Planned Activities

€ thousand ACT PY
Dec
21
Growth
Total equity and capitalization difference 42 858 41 413 1 445 3%
A. Total working capital - 2 976 - 1 290 - 1 686 131%
I. Trade net working capital 3 624 5 177 - 1 553 -30%
1. Inventories 4 080 4 598 - 518 -11%
2. Receivables and other assets 4 258 3 581 677 19%
3. Accounts payables - 4 714 - 3 002 - 1 712 57%
II. Prepaid expenses 514 443 70 16%
III. Other liabilities - 836 - 724 - 112 16%
IV. Other accruals - 6 277 - 6 186 - 91 1%
B. Long-term assets 15 884 14 886 998 7%
I. Intangible fixed assets 15 547 14 691 855 6%
II. Tangible fixed assets 16 19 - 3 -15%
III. Deferred tax assets 322 176 146 83%
C. Net cash 29 949 27 817 2 132 8%
I. Pension accruals - 2 502 - 2 423 - 79 3%
II. Financial assets 779 784 - 5 -1%
III. Tax accruals - 551 - 384 - 167 43%
IV. Cash 32 223 29 840 2 383 8%
  • Total working capital negative.
  • Inventories with normal monthly fluctuation.
  • Receivables higher in June due to high portion of sales end of month.
  • Increase in fixed assets driven by further milestone payments for development projects.
  • Increase net cash driven by profit and lower working capital.
  • Equity increased due to profit. Purchase of own shares (EURm 0.9); equity ratio at 73.1%.

Strong cash generation in H1 2022 based on sales development and lower working capital

€ thousand ACT PY
H1 21
Growth
Cash BoP 29 840 8 059 21 781 270%
Operating flow 4 953 2 660 2 292 86%
Net profit 2 351 - 2 197 4 548 107%
Depreciation & amortization 859 761 98 13%
Accruals 144 - 470 614 31%
Inventories & receivables - 230 - 2 945 2 715 -92%
Payables 1 824 3 275 - 1 451 -44%
Taxes 167 94 73 77%
Interests 17 381 - 364 -96%
Other - 180 3 761 - 3 942 -105%
Investing flow - 1 697 - 328 - 1 369 417%
Financing flow - 872 20 121 - 20 994 -104%
Cash EoP 32 223 30 512 1 711 6%
Change in cash and cash equivalents 2 383 22 453 - 20 070 -89%
  • Higher sales in H1 compared to previous period and IPO costs last year main driver of profitability increase.
  • Inventory build-up was higher in H1 2021 compared to H2 2022.
  • Investing cash flow for milestone payments.
  • Financing cash flow represents the buy-back of shares.

Single Pill Portfolio and Pipeline

APONTIS PHARMA: The Single Pill Strategy – Repeating Success

APONTIS expertise and market access meets demand for Single Pill development of commonly prescribed drugs available only as loose combinations

14

14

The Development of a Single Pill: Many Steps – One Goal

Short-term Pipeline: Accelerating the Development of Single Pills

1
Field of
application
AmloAtor RosuASS Tonotec Lipid Rosazimib
(AP –
D 01)
Caramlo HCT
(AP –
T 01)
Caramlo Lipid
(AP –
T 02)
Planned market launch Launched in May 2022 Launched in July 2022 Launched in May 2022 Q2 2023 Q3 2023 Q4 2023
Update August 2022 Q1 2024 Q3 2024
Status §
Launched in
Germany
§
Launched in
Germany
§
Launched in
Germany
§
Application for
Marketing
Authorization
submitted
§
Application for
Marketing
Authorization
submitted
§
Development
ongoing
§
Application for
Marketing
Authorization
expected in Q4 2022
Competitive environment §
No other Single Pill
provider with this
combination
§
No other Single Pill
provider with this
combination
§
No other Single Pill
provider with this
combination
§
Other Single Pill
provider with this
combination
§
No other Single Pill
provider with this
combination
§
No other Single Pill
provider with this
combination
Min. patient
potential²
510k 100k 230k 60k 180k 140k
Total
development cost
EURm 0.3
(exclusive licensing
agreement)
EURm 0.4
(semi-exclusive
licensing agreement)
EURm 1.9 EURm 0.0
(exclusive licensing
agreement)
EURm 1.3 EURm 2.5
Mid-term annual revenue
potential
EURm 3.2 EURm 2.5 EURm 5.0 EURm 3.0 EURm 9.0 EURm 3.0

Notes: (1) Main application essential hypertension; (2) Patient potential: Number of patients with same substance class combination in loose form Source: Patient INSIGHTS Analytics (PIA). A web-based pharma tool from INSIGHT Health GmbH & Co. KG; Company information

Licensed-in

own development

16

Mid-term Development Pipeline: Continuous Market Opportunities

Development candidates (n = 13) (Exclusive) In-Licensing agreements (n = 17)

AP - T 11 to be discussed 25 3,0-4,0

Product Patient potential
Revenue potential
Product
Projekt status
Projekt status
(narrow-Germany)
(narrow-Germany)
(in k, substance level)
(in EURm, peak sales)
Patient potential
(narrow-Germany)
(substance level)
Revenue potential
(narrow-Germany)
(in EURm, peak sales)
AP -
D 05
30 projects
in progress
AP -
D 01 (Rosazimib)
MAA submitted
in development
680
8,0-10,0
70 2,5
AP -
D 06
AP -
D 02
in negotiation
in development
585
7,5-9,5
10 1,0
AP -
D 07
AP -
D 03
in advanced
negotiation
in development
610
19,0
65 8,0-10,0
AP -
D 09
AP -
D 04
in negotiation
in negotiation
260
7,3
10 2,0-3,0
AP -
D 10
AP -
D 08
in negotiation
in negotiation
425
6,0-8,0
40 6,0-8,0
AP -
T 01 (Caramlo HCT)

3
in registration
AP -
D 11
in negotiation
MAA submitted
155
6,0-8,0
590 8,0-10,0
AP -
T 02
(Caramlo Lipid)
AP -
D 12
in negotiation
MAA submitted
115
6,0
AP -
D 13
in negotiation
880
95
7,7
1,7
AP -
T 03

4
in development
in development
20
11,6
AP -
D 14
in negotiation
60 4,0
AP -
T 04
to be discussed
150
5,0-6,0
AP -
D 15
to
be
discussed
90 4,0-5,0
AP -
T 05
to be discussed
35
3,0-4,0
AP -
D 16
to be discussed
100 0,8 -1,6
AP -
T 06

10
in negotiation
AP -
D 17
to
be
discussed
to
be
discussed
30
5,0
120 2,5-3,5
AP -
T 09
AP -
D 18
in negotiation
in negotiation
125
4,5-5,5
70 2,0-3,0
AP -
T 12

13
in discussion
AP -
T 07
in negotiation
in negotiation
15
5,0-6,0
95 2,5-3,5
AP -
T 08
in negotiation
95 7,5-8,5
AP -
T 10
in negotiation
30 2,4

Single Pill Outlook

Scientific

New publications at the Congress of the European Cardiology Society (ESC) by end of August 2022 START:

• Additional Data from START Data Base to support Single Concept

SECURE (prospective study):

• Comparison of Single Pill Iltria® (Ramipril/ Atorvastatin/ASA) vs. usual care

Commercial

Expansion of Marketing and Sales activities

  • Increasing number of scientific events and digital activities
  • Higher number of salesforce calls in second half of 2022 expected
  • Increasing acceptance of substitution activities as a result of new launches

Potential COVID-19 impact on access to physicians for patients and sales force, and on new launches caused by regulatory delays in the approval process

FY22 Forecast confirmed

Notes: * EURk 500 stock in trade increase at wholesaler with approx. EURk 325 gross profit impact Source: Company information, audited financials

Vision: To Establish the Single Pill as the Gold Standard. For a better life. Together. Every day.

  • Increasing acceptance of the Single Pill concept by physicians
  • Greater awareness of Single Pill company APONTIS PHARMA driven by growing portfolio
  • Strong support from key opinion leaders and scientific experts and call for action for Single Pill concept based on convincing study results (retrospective and prospective)

Increasing importance of Single Pill concept underpins strategy of APONTIS PHARMA

THANK YOU FOR YOUR ATTENTION!

[email protected] T: +49 2173 89 55 4900 F: +49 2173 89 55 1521

Alfred-Nobel-Str. 10 40789 Monheim am Rhein Germany

apontis-pharma.de

Talk to a Data Expert

Have a question? We'll get back to you promptly.