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Gentian Diagnostics ASA

Investor Presentation Aug 25, 2021

3604_rns_2021-08-25_a0107882-432d-4ea5-be85-edf85013ec3d.pdf

Investor Presentation

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H1 & Q2 21 Presentation

August 25th, 2021

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.

Today's presenters

Hilja Ibert

CEO

Njaal Kind CFO & COO

Introduction and Q2 highlights

Gentian's value proposition

The growing diagnostic market puts increasing pressure on laboratories. Still, many of the existing, clinically relevant biomarkers are only available on slow and inefficient platforms.

By converting biomarkers to the most efficient automated, high-throughput analysers, Gentian contributes to saving costs and protecting life.

Portfolio of high-impact tests provides solid growth opportunity

7* tests contributing to saving costs and protecting life

Revenue ambition of NOK 1bn in 5-7 years

Delivered ~30% annual revenue growth 2017-20

7 diagnostic tests, including two potential blockbusters

Ageing and growing population driving diagnostics demand

Market outlook Key drivers

• Increasing average age and population growth drives increase in chronic diseases and infectious diseases globally

Serviceable market

  • Gentian's selective approach, targeting attractive segments
  • GCAL® addressing severe infections and inflammations, providing exposure to one of the diagnostic industry's highest growing segments

Gentian market share

  • High-value biomarkers offering clinical benefits
  • Attractive solution to improve laboratory productivity

Addressable Market: Total demand within targeted markets 2020 (Kalorama 2020). Serviceable Market: The segment of the TAM targeted by Gentian's products (company estimates). Gentian's target market share is ~15-20%. Share of revenues net of partner take is 30-50% on average with product variations. Market growth rates = CAGR.

Ambitions for impact, high growth and value creation

Market opportunity and long-term ambitions Strategic pillars

5-7 year revenue ambition NOK 1bn

60%+ Gross margin at volume production

Long-term EBITDA margins 40%

  • Grow annual revenue from established products through additional commercial partners and regulatory approvals
  • Prove clinical relevance of GCAL® for the early detection of severe infections, which supports the avoidance of sepsis and the severity assessment of COVID-19 patients
  • Launch one new product per year; SARS-COV-2 Ab scheduled for Q4 2021 and NT-proBNP for Q1 2022
  • Secure one new contract with a global commercial partner per year, building on established partnerships
  • Grow gross margin through economies of scale
  • Deliver healthy long-term EBITDA margins through operational leverage and cost discipline

Q2 2021 highlights

Sales EBITDA
NOK 25m NOK -1m
+48% vs Q2'20 NOK -1m vs Q2'20
Cash Profitable
NOK 139m pre-R&D
NOK -22m vs Q2'20 based on current revenue from
four established products
  • Record total revenues of NOK 31.5m in Q2 21 and NOK 55.7m for H1 21
  • EBITDA for 2Q21 was MNOK -0.8 including MNOK 3.5 of costs related to the transfer of listing to Oslo Børs
  • Sales revenue of NOK 24.6m in Q2 21, a 48% growth compared to Q2 20. Organic growth was 65%*. Sales growth for H1 21 was 35% with corresponding organic growth of 47%
  • Development of the SARS COV-2 assay is on track for launch in Q4 21 and recent market data confirm the need for a high throughput test
  • The Gentian share was successfully transferred to Oslo Børs on June 25th

Operational review and growth opportunities

Sales growth driven by broad-based progress with commercial partners

  • 48% sales growth (65% organic) driven by strong development for all products capturing shares in Europe and Asia
  • Established products Cystatin C, fCAL ® turbo, c-CRP and fPELA addressing serviceable market of ~USD 200m, estimated to grow by 5-10% annually
  • Significant room to expand market access through additional commercial partners
  • Targeting 20%+ annual growth from the established products

GCAL® market development efforts focusing on validation

About GCAL ®

The early inflammation and infection biomarker GCAL ® is the first calprotectin test available on high-throughput analysers, with first sales realized in 2019. Clinical studies confirm the potential of GCAL ® for the early detection and prediction of severe infectious diseases. Sepsis kills 11 million people each year, and fast results provided by GCAL ® could save lives and significantly reduce healthcare costs.

  • New biomarker, requiring adoption by key opinion leaders, public and private laboratories
  • Serviceable market of ~USD 300m, estimated to grow by 15% annually
  • 6 ongoing studies to confirm GCAL's clinical relevance for supporting the avoidance of sepsis and the severity assessment of COVID-19 patients
  • At least 2 publications expected during H2 21
  • In addition, results from COVID-19 study with four hospitals in Spain to be presented at Euromedlab meeting in Dec 21
  • Validation of additional clinical chemistry platforms to drive further the commercial roll-out; 2 additional instruments expected in H2 21
  • Ongoing dialogue with potential global commercial partners

Upcoming product launches progressing as planned

About SARS-CoV-2 Ab

The aim with SARS-CoV-2 Ab, measuring COVID-19 immunity, is to offer the first such test for high-throughput analysers with focus on commercialisation in the Nordic markets.

About NT-proBNP

Gentian's NT-proBNP is the first test to support diagnosis of congestive heart failure available on high-throughput analysers – contributing to better diagnosis, monitoring and treatment.

  • On track for launch of SARS-COV-2 Ab in Q4 21
  • Preparations for transfer into validation phase ongoing
  • Serviceable market of USD 20m in the Nordics
  • The Norwegian Ministry of Health and Care Services, has made a change in regulations that allows for the use of antibody tests to assess immunisation levels of vaccinated individuals
  • NT-proBNP scheduled for launch Q1 22
  • Conclusion on reference method for standardisation on track for Q3 21
  • Outcome of reference method will impact rollout
  • Serviceable market of USD 800m, estimated to grow by 5-8% annually
  • Limited contingency included in project plans
  • Further 3 biomarkers addressing inflammations and infections, and cancer, currently in exploration and 'proof of concept'

Regulatory update: IVDR being introduced in 2022

  • The market Gentian operates in is highly regulated and the company must at all times comply with current legislation
  • A new legislation is being introduced in Europe from May 2022
  • The current in vitro diagnostic directive will be replaced by a new in vitro diagnostic regulation (IVDR)
  • The regulatory environment in Europe will be tightened, increasing the regulatory responsibilities of in vitro diagnostic manufacturers
  • Gentian's implementation of the regulation is on track according to the timeline in an established milestone plan, and the company expects to complete the IVDR certification by 26th of May 2022 to ensure continued supply of products in accordance with IVDR
  • The introduction of IVDR is expected to have limited impact on established products as Gentian is well prepared for the new regulation; for future launches there is a potential for industry wide bottlenecks based on external capacity with notified bodies

On track for one new global commercial partnership per year

Partnerships prove viability of go-to-market model

Long-standing commercial partnership for Cystatin C

Partnership for fCAL initiated through Bühlmann Laboratories

  • Adding one new resource to strengthen partner efforts
  • Dialogue to extend existing partnership for one additional product ongoing
  • Ongoing dialogue with 6 potential new global partnerships
  • On track for closing one new global partner for one Gentian product per year

Collaboration agreement for Canine CRP

Stable gross margin expected next 18 months

3 NOKm

NOKm

  • Ambition for 60% gross margin at volume production
  • Expect COGS in % of sales to decline over time as sales grow and new products at higher margin increases as percentage of total sales
  • Stable gross margin levels expected in 2021 and 2022 with quarterly variations driven by customer and product mix
  • Ambition for 40% long-term EBITDA margin
  • Plan to continue to increase investments throughout 2021 and 2022 to commercialize GCAL® and NT-proBNP

Financial review

Financial highlights

NOKm Q2 2021 Q2 2020 H1 2021 H1 2020
Sales 24.6 16.6 44.2 32.9
Other
revenues
6.9 3.2 11.5 6.1
Total revenues 31.5 19.9 55.7 39.0
COGS 11.4 6.3 21.8 16.2
Employee benefit expenses 8.7 9.4 18.4 18.4
D&A 2.0 1.6 4.0 3.1
Other OPEX 12.3 3.9 18.3 9.1
EBITDA -0.9 0.2 -2.8 -4.7
EBIT -2.8 -1.3 -6.8 -7.8

Sales and other revenues

  • Total revenue of NOK 31.5m in the quarter, up 58% vs Q2 20
  • 65% organic sales (48% reported) growth driven by broad-based progress with commercial partners across product portfolio
  • Established products Cystatin C and fCAL® turbo experienced strong demand growth in Asia and Europe
  • Other revenue growth driven by increased investments in R&D, boosting amounts received from grants and tax incentives

Sales - geographic split

NOKm Q2 21 Q2 20 H1 21 H1 20
US 1.0 1.0 1.4 1.7
Europe 15.7 9.9 29.7 21.1
Asia 7.9 5.7 13.1 10.1
Total 24.6 16.6 44.2 32.9

Sales - product split

NOKm Q2 21 Q2 20 H1 21 H1 20
Cystatin C 11.1 8.5 18.5 15.0
fCAL® turbo 8.3 3.9 16.7 9.2
Other 5.2 4.3 9.0 8.7
Total 24.6 16.6 44.2 32.9

Operating expenditures in the quarter

OPEX

NOKm Q2 21 Q2 20 H1 21 H1 20
Sales and marketing
expenses
3.7 3.0 7.8 6.4
Administration
expenses
8.9 6.0 14.4 11.0
Research
and
development expenses
10.7 5.0 18.3 10.7
Total 23.3 14.0 40.5 28.1
  • OPEX increased by NOK 9.3 million vs Q2 20
  • Listing cost estimated to NOK 3.5 million booked in Q2
  • Increase in R&D spend primarily driven by development of SARS COV-2 and NT-proBNP assays
    • Partially offset by NOK 3.7 million increase in other revenue

Strong cash position; fully financed business plan

NOKm Q2 21 Q2 20 H1 21 H1 20
Operating activities -2.9 1.1 -11.8 -8.6
Investing
activities
-4.0 -1.2 -6.2 -1.7
Financing
activities
-0.6 -0.1 -1.2 -0.1
Changes in cash and cash equivalent -7.5 -0.2 -19.2 -10.4
Cash
and cash equivalent at the beginning of period
146.1 161.4 158.0 171.6
Cash
and cash equivalent at the end of period
138.6 161.2 138.6 161.2

Summary and outlook

Several de-risking milestones next ~18 months

ESTABLISHED PRODUCTS GCAL® SARS-COV-2 AB NT-PROBNP
S Targeting additional large
commercial partners
Clinical studies confirming
relevance for early detection of
infections and with this the
Successful validation and
launch, scheduled for Q4 2021
Successful verification during
2021
E
N
O
T
S
E
L
Additional regulatory approvals,
including IVDR*
support to avoid sepsis and the
severity assessment of COVID
19 patients –
6 ongoing
Entering commercial
partnerships for the Nordics
Publication on the reference
method for standardisation
MI
022
021-2
Securing endorsements from
key opinion leaders
Successful validation and
launch, scheduled for Q1 2022
2 Securing global commercial
partnerships and continuation
of EU rollout
Securing endorsements
from
key opinion leaders and
global commercial
partnerships

Further potential milestones in pipeline with 3 biomarkers currently in exploration and 'proof of concept'

* IVDR: A new regulation coming into force 26 May 2022, requiring extensive documentation of the safety, performance and quality of each diagnostic test from manufacturers through several studies on both analytical and clinical performance.

Q&A

Appendix

Gentian Diagnostics develops and supplies innovative and efficient reagents for the clinical diagnostics market

  • Gentian serves the global market for human and veterinary clinical diagnostic tests
  • Expertise and focus within immunochemistry, specifically in the disease areas infection, inflammation, kidney failure and congestive heart failure
  • Gentian's innovative and efficient reagents can be used on all major clinical chemistry analysers, meaning no extra investments is required by the customer
  • Sales mainly through global commercial partners, which are serving the laboratories being the end users
  • 5 products launched to date and two further launches scheduled for Q4 2021 and Q1 2022, respectively
  • Preparing to scale with a fully funded business plan

Founded 2001

Employees

~50

Revenue 2020 NOK 79m Up 32% OSE: GENT

~NOK 0.9bn

How Gentian contributes to efficient diagnostics for better treatment decisions

The industry challenge

A growing diagnostics market puts increasing pressure on clinical laboratory efficiency

Many of the existing, but clinically relevant biomarkers are available only on slow and inefficient platforms

Hours from initiation of analysis to results

Gentian's solution

Particle-enhanced turbidimetric immunoassays (PETIA) based on proprietary nanoparticle technology and knowhow

Converting existing biomarkers to the most efficient automated, high-throughput analysers

10 minutes from initiation of analysis to results

3-10x higher throughput significantly improves laboratory productivity and costefficiency

Early disease detection and faster availability of clinically relevant information leads to better treatment decisions

Products targeting large and growing disease groups

DISEASE GROUP PRODUCT APPLICATION ATTRACTIVE CLINICAL BENEFITS
Kidney
disease
Cystatin C Early detection of reduced kidney function Preventing severe kidney failure
Inflammation
& infection
fCAL Fast diagnosis of inflammatory bowel disease Reducing time-consuming and costly colonoscopy
GCAL Early detection of severe infections, including sepsis Reducing chance of fatality and treatment costs
SARS-CoV-2 Ab Measuring COVID-19 immunity Supporting community management
Canine CRP Early detection and diagnosis of inflammation in dogs High relevance of results due to dog specific CRP
Cardiac NT-proBNP Diagnosis, monitoring and assessment
of congestive heart failure
Contributing to standardization
of NT-proBNP
assays
Pancreas fPELA Diagnosis of pancreatic elastase insufficiency
in combination with fCAL
Reducing time-consuming
and costly colonoscopy

USD 1.3bn global serviceable market estimated to grow by 8-9% annually next 5-7 years

Total Addressable
Market, USDbn
Total Serviceable
Market, USDm
Target market share,
unrisked
Gentian's
revenue take
Serviceable Market
annual growth rate,
next 5-7 years
Established products 1.5 180 ~25% 30-50% 5-10%
GCAL 2.0 300 ~15% 30-50% 15%
NT-proBNP 1.6 800 ~15% 30-50% 5-8%
SARS-CoV-2 Ab 2.0 20 ~25% 50% n.m.
Total 7.1 1,300 15-20% 30-50% 8-9%

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

Combining avian antibodies and PETIA enables fast results and improved lab productivity

Avian antibodies

Avoiding interference enables conversion to PETIA

Antibodies: Proteins used by the immune system to identify bacteria and viruses

Avian antibodies: Extracted from hen eggs. Avoids interference due to lack of complement system binding antibodies and molecules, enabling analysis at lower concentrations than mammalian antibodies and conversion of existing biomarkers to PETIA

Advantages: Gentian uses avian antibodies when applicable and believes extraction from eggs rather than puncturing animals contributes to better animal welfare while also offering a cost advantage at scale

PETIA

Removing separation steps increases throughput and reduces cost

Immunoassays: Biochemical tests measuring molecule presence or concentration in human cells using an antibody

Particle-enhanced turbidimetric immunoassays: Enables moving immunoassays from low-volume to high-volume clinical analysers

Advantages: Moving immunoassays to PETIA enables removing separation steps, which increases throughput and laboratory efficiency compared to the traditional ELISA and other methods

Structured approach to product development

Diversified sales model to ensure broad market access and maximize penetration

Global diagnostics companies Specialized/local distributors Healthcare providers

  • Gentian's main strategy to secure broad roll-out and acceptance of product
  • Beckman Coulter and Bühlmann/Roche Diagnostics are current partners falling into this category
  • Ambition to secure one new contract with global commercial partner per year

  • Accelerating time to revenue and awareness

  • Distribution agreements in several European countries and South Korea for GCAL, Cystatin C and Canine CRP

  • Direct sales to select end-users and key opinion leaders, including laboratory and hospitals

  • Sales representatives in US, Sweden and HQ in Norway
  • Sales office in Sweden distributes Gentian and Bühlmann Laboratories complimentary products

Gentian management

CEO Hilja Ibert

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. Dr. Ibert holds a PhD degree in Nutrition Science from the University of Bonn, Germany.

CSO Erling Sundrehagen

Erling Sundrehagen, cofounder of Gentian, holds 25 int. patents. He has headed the development of a dozen diagnostic products, creating businesses with NOK 1bn+ revenue. Dr. Sundrehagen held management positions in Axis-Shield, Axis Biochemicals and Axis Research, and is dr.med. & cand.real from University of Oslo, Norway.

CFO & COO

20+ years experience and

financial management and reporting, corporate governance and Investor Relations. Mr. Kind has served as the CFO for

in Eramet Comilog Manganese, France, and Investment Director in Tinfos. Kind holds a MSc from BI Norwegian Business School.

Njaal Kind

VP R&D Torsten Knüttel

extensive track-record from TiZir, UK, Business Analyst 18+ years' experience from the diagnostic industry and commercial supply chain. His background includes OEM/B2B business development at Thermo Fisher Scientific and development and production at GE Healthcare. He holds a PhD in Chemistry from the Leibniz University Hannover, Germany.

VP Clinical Affairs Alexandra Havelka

Extensive experience in laboratory medicine. She was previously Biochemist and Unit Manager at Karolinska University Laboratory, with research focusing on biomarkers for inflammation and infection. Dr Havelka holds a PhD in Experimental Oncology from Karolinska Institute in Stockholm, Sweden.

VP Global Sales Markus Jaquemar

30+ years experience in life science and diagnostics commercialisation and marketing. He held marketing, sales and business management positions at Beckman Coulter, Agilent Technologies and Becton Dickinson. He holds a Master's degree in Biology from Vienna University, Austria.

VP QA & RA Anne-Mette Horsrud Akre

20+ years of pharma industry experience, including production of pharmaceuticals and medical devices, quality management and assurance and management positions at GE Healthcare and Fresenius Kabi. She holds a Msc in Biotechnology from the Technical University of Trondheim,

VP BD Jack Andreassen

20+ years of experience from sales, market and business development from the global diagnostics industry. He was previously Associate Director, Global Market Development for OEM at Thermo Fisher. He holds a Msc in Chemistry, Biochemistry/Molecular Biology from the University of Oslo, Norway.

Norway.

Gentian board

Tomas
Settevik
Espen Tidemann
Jørgensen
Ingrid Teigland
Akay
Kari E.
Krogstad
Susanne
Stuffers
Runar
Vatne
Tomas
Kramar
Chair of
the Board
Board member Board member Board member Board member Board member Board member
Tomas Settevik
has
experience in both life
sciences and retail and is
currently an independent
investor and non-exec
director in several
companies. He was
previously CEO of
Stokke, and CEO of
Pronova
BioPharma
after
serving as Vice President
Pharmaceuticals and
Manufacturing. Mr.
Settevik
has also held
several senior positions –
VP Northern Europe, VP
Marketing and R&D, and
Managing Director
UK/Nordic –
at Tyco
Healthcare EMEA. Mr.
Settevik
holds a degree
from Copenhagen
Business School.
Espen Tidemann
Jørgensen is currently
Portfolio Manager of
Holta Invest and
Managing Director of
Holta Life Sciences. He
has 18 years of financial
markets experience as
equity analyst at DNB
Markets and investor. Mr.
Jørgensen was
previously member of the
Board of Directors at
Weifa
and Cortendo, and
is currently board
member at Decisions.
Mr. Jørgensen holds a
Msc
in Economics and
has completed 3 years of
Medicine studies at the
University of Oslo.
Ingrid Teigland
Akay
is a
life science investor and
medical doctor. She has
previously served as a
Senior Investment
Manager at Inventages.
Ms. Akay
has broad
clinical experience in
internal medicine and
surgery at Scandinavian
and UK hospitals. Today
she is Managing Partner
of Hadean
Ventures, a
life science investment
firm with focus on the
Nordics. Ms. Akay
holds
a medical degree from
Medizinische
Hochschule
Hannover and an MBA in
Finance from London
Business School.
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.
Susanne Stuffers is
currently managing
partner of P53 Invest AS.
Previously she was an
equity analyst with Arctic
Securities covering the
healthcare sector, and
management consultant
at EY. Ms. Suffers has
held medical and
commercial roles at
Novartis and has had
clinical practice as a
resident in oncology at
OUS Ullevål. Ms. Stuffers
holds an M.D. degree
from the Erasmus
University Rotterdam and
a Ph.D. degree in cancer
biomedicine from the
Norwegian Radium
Hospital.
Mr. Vatne
is the principal
and owner of Vatne
Capital, a family office
investing in financial
assets and real estate.
He is co-founder of
Søylen
Eiendom, a
leading Oslo based real
estate company, and
was previously partner
and stock broker in
Pareto Securities. Mr.
Vatne
also serves as
board member of listed
companies Solon
Eiendom
ASA and Self
Storage Group ASA.
Vatne
and associated
companies currently own
14.49% of the
outstanding shares in
Gentian Diagnostics
AS.
Mr. Kramar
has more
than 40 years of
experience from the
diagnostic industry
including Siemens,
Abbott and Roche
Diagnostics. Mr. Kramar
has held several senior
positions like Global
Business Manager,
Business Director and
CEO, as well as being a
founding partner in the
Kramar
Group. In
addition, Mr. Kramar
has
held several board
positions over the
years.
Mr. Kramar
holds
an MSc degree in
Chemistry from the
Faculty of Engineering at
Lund University in
Sweden.

Top 20 shareholders

Shareholder No of Shares %
Vatne Equity AS 2 010 224 13,04 %
Norda ASA 1 250 068 8,11 %
Holta Life Sciences AS 1 188 702 7,71 %
Safrino AS 1 050 000 6,81 %
Verdipapirfondet Delphi Nordic 817 045 5,30 %
Salix AS 786 903 5,11 %
Skandinaviska Enskilda Banken AB 783 903 5,09 %
Verdipapirfondet Storebrand Vekst 425 572 2,76 %
Verdipapirfondet DNB SMB 377 682 2,45 %
Equinor Pensjon 337 320 2,19 %
Portia AS 300 000 1,95 %
Cressida AS 235 000 1,52 %
Lioness AS 220 000 1,43 %
Silvercoin Industries AS 214 692 1,39 %
Marstal AS 212 407 1,38 %
Mutus AS 210 465 1,37 %
Vingulmork Predictor AS 184 083 1,19 %
Bård Sundrehagen 181 645 1,18 %
OM Holding AS 179 000 1,16 %
Viola AS 170 916 1,11 %
Other Shareholders 4 276 262 27,75 %
Total Shares 15
411 889
100.00%

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