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Gentian Diagnostics ASA

Investor Presentation May 7, 2025

3604_rns_2025-05-07_0178a5f1-f1da-4ca9-85d4-c01fc153ea65.pdf

Investor Presentation

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Q1 25 Presentation

7 May 2025

Important notice

This presentation has been prepared by and is the sole responsibility of Gentian Diagnostics ASA (the "Company" or "Gentian"). The presentation is furnished to you solely for your information and may not be reproduced or redistributed, in whole or in part, to any other person. The information herein and any other material discussed is subject to change.

The presentation contains certain forward-looking statements relating to the business, future financial performance and results of the Company and/or the industry in which it operates. Forward-looking statements concern future circumstances and results and other statements that are not historical facts, sometimes identified by the words "believes", "expects", "predicts", "intends", "projects", "plans", "estimates", "aims", "foresees", "anticipates", "targets", and similar expressions. Any forward-looking statements contained herein, including assumptions, opinions and views of the Company or cited from third party sources are solely opinions and forecasts

which are subject to risks, uncertainties and other factors that may cause actual events to differ materially from any anticipated development. Potential investors are expressly advised that financial projections, such as the revenue and cash flow projections contained herein, cannot be used as reliable indicators of future revenues or cash flows. The Company (nor any of its parent or subsidiary undertakings) does not provide any assurance that the assumptions underlying such forward-looking statements are free from errors nor does any of them accept any responsibility for the future accuracy of the opinions expressed in this presentation or the actual occurrence of the forecasted developments. No obligation is assumed to update any forward-looking statements or to conform these forwardlooking statements to our actual results.

The distribution of this presentation may also in other jurisdictions be restricted by law. Accordingly, this presentation may not be distributed in any jurisdiction except under circumstances that will result in compliance with applicable laws and regulations. The Company require persons in possession of this presentation to inform themselves about, and to observe, any such restrictions.

Nothing in this presentation shall constitute an offer to sell or a solicitation of an offer to buy any shares in the Company in any jurisdiction in which such offer or solicitation is unlawful.

Nothing contained in this presentation is or should be relied upon as a promise or representation as to the future. Except where otherwise expressly indicated, this presentation speaks as of the date set out on its cover. In addition, no responsibility or liability or duty of care is or will be accepted by the Company for updating this presentation (or any additional information), correcting any inaccuracies in it which may become apparent or providing any additional information.

Efficient diagnostics for better treatment decisions

Gentian Diagnostics at a glance

A MedTech company targeting \$1.8Bn serviceable diagnostic market with 5-10% annual growth

Focused strategy, lean business model & appealing value proposition

Industry-leading capabilities - strong focus on inhouse R&D and Operations

At commercial phase and making profit

High quality standards (IVDR and ISO13485 certified) and focus on ESG

Gentian Diagnostics is listed on Euronext Oslo Børs, ticker: GENT

Appealing value proposition

Value proposition

Many clinically relevant diagnostic biomarkers are available only on slow and inefficient platforms

By leveraging existing, open-channel instrumentation, Gentian converts these tests to high-throughput analysers

Faster results → better treatment decisions

Up to 10x improved efficiency and cost savings

Lean business model

Partnerships with global IVD companies

OEM partnerships to secure broad roll-out and acceptance of product

Distributors in select markets

In selected markets we do not serve directly

Direct end-users

Large central laboratories in selected markets

Focused strategy targeting large, existing market with our world-leading knowledge on PETIA*

Highly specialised with PETIA assays on high volume diagnostic segments.

Addressing customer needs with worldclass R&D, production, clinical data generation and regulatory support.

Leveraging growing volumes, cost pressure and market consolidation trends.

Sustained growth with diverse product pipeline, technological improvements for PETIA, or via adjacent new technologies.

Key disease areas: inflammation & infection, kidney disease, heart failure

Key drivers for long-term growth and value creation

Five established products with potential to grow 20%+ annually

Prove clinical relevance of GCAL® and bring NT-proBNP to market

Bring a steady stream of new high-impact diagnostic tests to market

Secure one new contract with a global commercial partner per year

Grow gross margin from ~50% to 60%+ through economies of scale

Long-term EBITDA margins of 40%

revenue potential of NOK 1bn in 5-7 years Targeting a serviceable market of USD 1.8bn*

combined net

Highlights

1Q highlights: Record sales and profitability improvements

1Q25 financials and key milestones Additional highlights

Sales Gross margin
MNOK 44.5 64%
+16% vs 1Q24 53% in 1Q24
EBITDA
MNOK 14.0
MNOK 4.8 in 1Q24
Sales to Asia
+30% vs 1Q24
  • Gentian's business in China recovering well from H2 '24 softness (impact of Value Based Pricing tendering)
  • Cystatin C had the highest quarterly result ever (17.6 mNOK, +18% vs. Q1 '24) driven by China and US sales.
  • From "Other" category, fPELA, cCRP and GCAL experienced high double-digit growth in Q1 2025 vs. PY.
  • Gross margin improvement is a result of strong operational performance and scale effects from increased production
  • For our first-in-class turbidimetric NT-proBNP assay, calibration strategy has been decided, and the company continues with the development of an assay detecting total NT-proBNP not affected by glycosylation - creating the opportunity for clinical differentiation.

Both the US and Asia growing by ~30% followed by Europe

Highlights

  • Record sales with 16% growth (13% organic) vs. 1Q24.
  • Growth from all products and all geographic markets.
  • Sales of Cystatin C increased 18% in 1Q25 compared to 1Q24, mainly due to normalisation of supply to China.
  • Good momentum in the US continued in Q1 (+31% in 1Q25 vs 1Q24) driven by Cys C and cCRP.

Sales revenues (MNOK)

Sales revenue - geographic split

MNOK 1Q25 1Q24 2024
US 3.8 2.9 12.2
Europe 30.7 27.9 116.2
Asia 10.0 7.7 23.7
Total 44.5 38.5 152.1

Sales revenue - product split

MNOK 1Q25 1Q24 2024
Cystatin C 17.7 14.9 50.6
fCAL® turbo 14.8 13.7 61.3
Third-party
products
5.1 4.7 18.3
Other 6.9 5.2 21.8
Total 44.5 38.5 152.1

Stable cost development

OPEX Capitalised R&D expenses

Operating expenses

MNOK 1Q25 1Q24 2024
Sales and marketing expenses 6.1 6.4 28.1
Administration expenses 6.3 6.0 21.7
Research and development
expenses
5.1 6.1 21.9
Total 17.5 18.5 71.7
  • Operating expenses ended at NOK 17.5 million in 1Q25 compared to NOK 18.5 million in 1Q24
  • Capitalised R&D expenses was MNOK 2.0 in 1Q24 compared to MNOK 2.5 in 1Q24

Strong gross margin improvement crossing 60%

Gross and EBITDA margin % .

  • Gross margin increase factors:
    • Strong operational performance
      • Cost improvement initiatives
      • Productivity gains from scale advantages

▪ EBITDA margin increase factors:

  • Higher revenue base
  • Improved gross margin
  • Stable OPEX compared to 1Q24

Significant EBITDA improvement

EBITDA development (MNOK)

  • Significant EBITDA improvement in 1Q25 to NOK 14.0 million vs 4.8 million in 1Q24
  • Scale effects are materializing on current revenue level

Solid cash position

1Q25 balance sheet and cash flow

.

Cash Capex
MNOK 88.7 MNOK 2.0
MNOK 85.6 in 1Q24 MNOK 3.2 in 1Q24
FCF Equity ratio
MNOK 4.6 86.3%
MNOK -0.6 in 1Q24 81.2% in 1Q24

Capital priorities

  • NOK 4.0 million increase in cash from 31 December 2024
  • Solid cash position of 88.7 million
  • No interest-bearing debt
  • Long-term net working capital/sales assumed at ~30%

Product update

Cystatin C Record sales with growth coming from all markets

  • Cystatin C had the highest quarterly result ever driven by strong China and US sales.
  • Good momentum in China with a solid orderbook for Q2.
  • Received the largest Cys C order ever from South-Korea.
  • The USA: already 19 new Cys C customers added this year – a result of our direct sales efforts and improved collaboration with commercial partners capitalizing the positive KDIGO kidney guidelines update last year.

Sales of fCAL® turbo last 2 years (MNOK)

  • After record high Q4, fCAL grew +8% in 1Q25 compared to 1Q24.
  • Sales driven by growing demand for fecal calprotectin testing and market share gain from traditional ELISA tests.
    • Overall, the outlook for 2025 is positive.

Other products* delivering 33% YoY growth

Sales of other products last 2 years (MNOK)

  • Q1 sales of NOK 6.9 million, up 33% compared to Q1 last year
  • fPELA, cCRP and GCAL experienced high double-digit growth in Q1 '25 vs. Q1 '24.
  • Pivoting our GCAL focus on inflammatory rheumatic diseases (IRDs), while fine-tuning our positioning in the field of severe infections and sepsis prevention through targeted studies

Third-party products High single digit growth in Q1 2025

Sales of third-party products last 2 years (MNOK)

  • Q1 sales up by 9% compared to Q1 last year.
  • Increased presence in Finland and Denmark
  • Conversion of home-brew assays to IVDR certified assays
  • Agreement with Thermofisher for distribution of cCRP in Sweden

All regions delivering good growth – Asia back on track after soft H2 2024

R&D update and summary

NT-proBNP development proceeding as planned

A Total NT-proBNP calibration option selected for further development

About NT-proBNP

Measuring NT-proBNP levels support diagnosis of heart failure. The Gentian assay will be the first test of its kind available on high-throughput analysers which should increase laboratory productivity and reduce overall costs. Additional benefit may include addressing underserved needs especially with specific patient subgroups.

1Q highlights:

  • Based on expert opinions and preliminary clinical evaluation, a calibration strategy has been decided, and the company continues with the development of an assay detecting total NT-proBNP not affected by glycosylation. This assay will report unique values and will rely on new clinical cut-offs
  • Unpredictable and individual variation in glycosylation of NT-proBNP creates the opportunity for clinical differentiation using the Gentian NT-proBNP assay, especially in underserved patient subgroups. The company is currently investigating the scope for clinical evidence generation.
  • Significant progress is made in the assay development. The aim is to introduce the assay as a research-use-only product in the second half of 2025 and full commercial launch in 2026 (depending on regulatory timelines).
  • Patent application in Japan is accepted protecting Gentian's innovative approach to NT-proBNP measurement using turbidimetric immunoassay technology.

Q&A

Appendix

P&L highlights

MNOK 1Q25 1Q24 2024
Sales 44.5 38.5 152.1
Cost of goods sold -16.1 -18.2 -69.3
Gross profit 28.4 20.3 82.8
Other
revenues
0.9 0.8 4.6
R&D expenses -5.1 -6.1 -21.9
Sales and marketing expenses -6.1 -6.4 -28.1
Administrative expenses -6.3 -6.0 -21.7
Operating profit 11.7 2.6 15.7
Net financial
items
-1.6 1.6 4.3
Net profit (loss) 7.8 4.2 45.3

Balance sheet highlights

MNOK 1Q25 1Q24 2024
Inventory 52.3 36.6 45.9
Accounts-
and other receivables
29.6 22.8 31.3
Cash and cash equivalents 88.7 85.6 84.7
Total non-current assets 65.3 41.6 67.7
Total assets 235.9 186.6 229.7
Total paid-in equity 317.2 314.5 316.3
Total retained equity -113.8 -163.1 -122.2
Total equity 203.5 151.4 194.1
Total
non-current liabilities
4.3 9.0 5.5
Total current
liabilities
28.1 26.2 30.1
Total equity
and liabilities
235.9 186.6 229.7

Cash flow highlights

MNOK 1Q25 1Q24 2024
Operating activities 6.6 2.6 13.5
Investing
activities
-2.0 -3.2 -11.0
Financing
activities
-1.3 -1.2 -5.0
Changes in cash and cash
equivalent
3.3 -1.8 -2.4
Cash
and cash equivalent at the
beginning of period
84.7 87.6 87.6
Cash
and cash equivalent at the
end of period
88.7 85.6 84.7

Achieved 26% p.a. sales growth last six years

0

20

40

60

80

100

120

140

160

Partnerships prove viability of go-to-market model

Global distribution agreement for GCAL®, initial roll-out in Europe

Long-standing commercial partnership for Cystatin C

Partnership for fCAL®turbo initiated through Bühlmann Laboratories

USD 1.8bn global serviceable market estimated to grow by 5-10% annually next 4-6 years

Total Addressable
Market, USDm
Total Serviceable
Market, USDm
Target market share,
unrisked
Gentian's
revenue take
Serviceable Market
annual growth rate,
next 4-6 years
Established products 2,220 240* ~25% 30-50% 5-10%
GCAL infection
(sepsis)
1,000 440 ~15% 30-50% 7%
GCAL inflammation 1,250 250 Under evaluation 30-50 Under evaluation
NT-proBNP 1,700 900 ~15% 30-50% 5-10%
Total 6,100 1,830 >15% 30-50% 5-10%

Key risks to target market shares include market adoption rates for GCAL, and successful launch of NT-proBNP

Dedicated and experienced management team

CEO Matti Heinonen

CFO & COO Njaal Kind

CSO

CTO Dr. Frank Frantzen Dr. Alexandra Havelka

VP R&D Dr. Torsten Knüttel

VP QA & RA Anne-Mette Horsrud Akre

20+ years of relevant industry experience across management positions

Track record from leading global diagnostics companies in across all phases

CCO Markus Jaquemar

Board of directors

Hilja
Ibert
Kari E.
Krogstad
Kjersti
Grimsrud
Runar
Vatne
Christian
Åbyholm
Chair of
the Board
Board member Board member Board member Board member
Dr. Hilja Ibert has more than 25
years' experience from the
international diagnostic
industry, including VP
International Diagnostic
Solutions at Hologic and senior
positions within Becton
Dickinson and bioMerieux. She
was previously the CEO for
miDiagnostics
in Belgium. In
2018, she was appointed CEO
of Gentian Diagnostics ASA, a
position she served until May
2024. She is currently a board
member in Gradientech
and
VitaDx.
Kari Krogstad has
more than 25 years of experience
from the biomedical industry,
from commercial leadership roles
within the pharma, biotech and
medtech
sectors. Ms. Krogstad
has held her current role as
President and CEO at Medistim
ASA since 2009. She was
previously General Manager at
Invitrogen Dynal. Ms. Krogstad
holds a Cand. Scient. degree in
Molecular Biology from the
University of Oslo as
well as a Business degree from
IHM Business School.
Kjersti Grimsrud is currently President and
COO of Infusion care at Convatec
plc,
where she has spent the last 5 years. She
has over 30 years' experience in MedTech
and IVD companies with roles in science,
operations and commercial in Axis-Shield
ASA and Alere Inc./Abbott, where she last
held the position of VP Commercial EME
(Europe Middle East)
and International (APAC). Ms Grimsrud
served as a board member of Biotec
Pharmacon
(now ArcticZymes
technologies)
from 2011 to 2015. Ms. Grimsrud holds a
master's degree in biotechnology from the
Norwegian University of Science and
Technology
in Trondheim.
Mr. Vatne is the principal and owner of
Vatne Capital, a family office investing in
financial assets and real estate. He has
extensive experience from the real
estate sector, primarily from Søylen
Eiendom, a leading Oslo based real
estate company which he co‐founded in
2004. Prior to Søylen
Eiendom, Mr.
Vatne was a Partner and stock broker
in
Pareto Securities. Mr. Vatne served as
board member of Gentian Diagnostics
from November 2019 to May 2022.
Mr. Vatne and companies controlled by
him currently own 15.12% of the
outstanding shares in Gentian
Diagnostics ASA.
Christian Åbyholm is a partner in Kvantia
AS
where he joined in 2007. Prior to joining Kvantia
AS, Christian worked as Head of Department
within Mergers and Acquisitions in Norsk Hydro
and as Senior Vice President in business
development in Aker RGI. Christian has also
worked in London as an Associate in Equity
Research in Morgan Stanley where he was part
of the number one European Paper and
Packaging team ranked by Institutional Investor.
Prior to that, Christian worked as an Analyst in
Merrill Lynch's Investment Banking division.
Mr. Åbyholm is a CFA charter holder and has an
MBA from IMD and a Siviløkonom
degree from
Norwegian School of Economics and Business
Administration. In addition, Christian has
Dr. Ibert holds a PhD degree in
Nutrition Science from the
University of Bonn, Germany.
completed first two years of law school at
University of Oslo.

Caaby AS, a wholly owned company by Mr. Åbyholm owns 173,500 shares in the company. Kvantia AS and its subsidiaries (Victoria India Fund AS and Obligasjon 2 AS) own 1,992,208 shares in the company. In addition, Christian Åbyholm is Chairman in INSR ASA and Norda ASA, which both own 614,215 shares in the company. The combined shareholding corresponds to 22% of the outstanding shares in Gentian Diagnostics ASA.

Top 20 shareholders

Shareholder No of shares %
Vatne Equity AS 2 110 224 13.68 %
Kvantia AS 1 803 368 11.69 %
Carpe Diem Afseth AS 721 907 4.68 %
Verdipapirfondet Delphi Nordic 697 006 4.52 %
Safrino AS 649 700 4.21 %
Insr ASA 614 251 3.98 %
Norda ASA 614 251 3.98 %
J.P. Morgan SE 523 631 3.40 %
Verdipapirfondet Delphi Norge 384 572 2.49 %
Verdipapirfondet DNB SMB 344 957 2.24 %
Portia AS 300 000 1.95 %
Krefting, Johan Henrik 298 000 1.93 %
Viola AS 258 421 1.68 %
Intertrade Shipping AS 257 716 1.67 %
Cressida AS 235 000 1.52 %
Lioness AS 220 000 1.43 %
Marstal AS 212 407 1.38 %
Verdipapirfondet Storebrand Vekst 211 665 1.37 %
Mutus AS 210 465 1.36 %
Silvercoin Industries AS 187 455 1.22 %
Other Shareholders 4 567 354 29.62 %
Total Shares 15
422 350
100.00%

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