Regulatory News:
THERACLION (ISIN: FR0010120402; Mnemo: ALTHE), an innovative
company developing a robotic platform for non-invasive
high-intensity focused ultrasound (HIFU) therapy for the treatment
of varicose veins, reports on its 2024 activities.
- On-track progress of the pivotal FDA clinical trial
- Sharp increase in the number of scientific presentations and
publications
- Over 3,000 SONOVEIN® treatments performed to date
- Product maturity reached and commercialization
accelerated
Martin Deterre, Theraclion’s Chief Executive Officer, states,
"In 2024, Theraclion achieved key milestones in its strategy
focused on accessing the U.S. and Chinese markets and advancing a
market-ready SONOVEIN® product. In addition to the continued
progress of our FDA (Food&Drug Administration) clinical study,
SONOVEIN reached a new level of maturity, in particular in terms of
clinical efficacy and treatment speed1. Our product and our
business model are now proven, with an increasing number of
presentations and publications from KOLs. Looking ahead to 2025, we
are ready to shift gears towards commercialization and revenue
generation”.
Progress of the FDA-approved clinical study on
schedule
In the United States, the FDA-approved pivotal study for
SONOVEIN® reached a key milestone in mid-June, as treatments were
completed on schedule. The trial was conducted at four leading
centers across the United States and Europe and included 70
patients.
The 6-month follow-up period concluded in December 2024, marking
another important milestone in the study.
The 12-month follow-up is currently underway, with final results
expected by summer 2025. We plan to submit the marketing
authorization application to the FDA in the second half of 2025,
with approval estimated in the first half of 2026, subject to the
FDA’s schedule. These developments mark a critical step toward
entering the world’s largest market and unlocking strategic
partnership opportunities.
Progress in product maturity and scientific
presentations
Strong indications of growing market adoption have emerged this
year, with Sonovein vein treatments exceeding the milestone of
3,000 procedures performed.
2024 saw a new record reached, with 29 presentations on
SONOVEIN® delivered at 25 events across 11 countries. A total of 15
key opinion leaders shared their experiences with non-invasive
treatment of varicose veins using focused ultrasound. They
highlighted the adoption of SONOVEIN® in their daily practice.
In addition, three scientific papers on SONOVEIN® were published
in the high-impact factor Phlebology journal, and a chapter of the
5th edition of the Handbook of Venous and Lymphatic Disorders –
Guidelines of the American Venous Forum was dedicated to the
technology.
Furthermore, the completion of 400 procedures performed by a
treatment center that opened just two and a half years ago is also
one of the strongest indicators of the product's maturity in
2025.
Focus on strategic realignment on the vein market
Theraclion continues its strategic refocus on the varicose vein
market and confirms its decision to cease commercialization of its
Echopulse devices for thyroid treatment in the near future. At the
beginning of 2024, Theraclion announced its decision not to renew
CE marking for Echopulse in accordance with the new European MDR
regulations, which consequently affected various regulatory
approvals in Asia. In this context, while the Theraclion China
joint-venture focuses its efforts on commercial development of
SONOVEIN, Theraclion has decided to reclaim older-generation
Echopulse machines initially intended for the Chinese market. These
systems have become challenging to market due to the updated
strategy. In order to mitigate the impact on the joint venture,
Theraclion will issue a €680K credit note. Based on the latest
financial statements as of June 30, this transaction will result in
a reduction in trade receivables on the balance sheet, causing a
decrease in revenue and hence in net income of the same amount. The
reclaimed machines will be recorded as inventory at their original
value and will be fully depreciated. These accounting operations,
which pertain to prior fiscal years, will enable Theraclion to
finalize the impacts of discontinuing Echopulse
commercialization.
2024 turnover
The revenue for the year 2024, excluding an adjustment related
to the issuance of a credit note for the Echopulse activity
amounting to €680K, stands at €1,485K. This sustained activity
compared to the first half of 2024 is driven by the sale of a
Sonovein system in the Middle East and growth in recurring
revenue.
Sales of consumables and services increased by 9% compared to
2023, reflecting the growth in recurring revenue.
The sale of only one system in 2024 explains the -33% variation
compared to 2023.
Theraclion has so far focused on supporting centers equipped
with SONOVEIN® to enhance their experience rather than prospecting
for new clients. In 2024, the company allocated its resources to
improving products and treatment protocols, as well as clinical
trials to ensure the success of the U.S. clinical study.
Starting in 2025, given the progress made in clinical studies
and R&D, the company will focus on commercial development, with
a priority on Europe and the Middle East. With this initial
commercial rollout, Theraclion aims to achieve €2.5M in revenue in
2025 and €5M in 2026. Beyond 2026, once FDA approval is obtained,
the company anticipates an acceleration in sales driven by the
deployment of its commercial strategy in the U.S.
Sales / K€
2024
Before
adjustment (*)
2024
After
adjustment
2023
Variation
%
Sales of Sonovein systems
808
808
1 201
-33%
Credit Note to be issued for Echopulse
-
(680)
Sales of consumables
478
478
504
-5%
Sales of services
199
199
117
70%
Turnover Theraclion SA
1 485
805
1 822
-56%
Including veins
1 442
1 200
Including breast and thyroid
43
(637)
622
Other operating revenue
141
141
2
Licenses
2 000
Operating revenue total
1 626
946
3 825
-75%
(*) Credit note to be issued to the Theraclion China joint
venture for the return of Echopulse machines
Evolution of cash flow and going concern
As of December 31, 2024, Theraclion had a cash balance of €4.1
million, down from €5.9 million at end June 2024. This cash
position will cover Theraclion's needs until the beginning of the
second quarter of 2025.
The Company has already taken steps to secure the financing it
needs in order to pursue its strategy and begin its commercial
expansion. In the event that the Company is unable to obtain such
funding, its long-term viability could be at risk.
Next financial publication
Publication of the 2024 financial results on April 29, 2025.
About Theraclion
Theraclion is a French MedTech company committed to developing a
non-invasive alternative to surgery through the innovative use of
focused ultrasound.
High Intensity Focused Ultrasound (HIFU) does not require
incisions or an operating room, leaves no scars, and enables
patients to return to their daily activities immediately. The HIFU
treatment method concentrates therapeutic ultrasounds on an
internal focal point from outside the body.
Theraclion develops the HIFU, CE-marked, platform for varicose
veins treatment SONOVEIN®, which has the potential to replace
millions of surgical procedures every year. In the United States,
SONOVEIN® is an investigational device limited to investigational
use; it is not available for sale in the U.S.
Based in Malakoff (Paris), the Theraclion team is made up of
some 30 people, most of them involved in technological and clinical
development.
For more information, please visit
www.theraclion.com and follow the LinkedIn
account.
Theraclion is listed on Euronext Growth Paris Eligible for the
PEA-PME scheme Mnemonic: ALTHE - ISIN code: FR0010120402 LEI:
9695007X7HA7A1GCYD29
1 See published clinical results:
https://www.theraclion.com/wp-content/uploads/2024/12/Exhaustive-Publications-and-Presentations_18_12_24.pdf
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version on businesswire.com: https://www.businesswire.com/news/home/20250106661202/en/
Theraclion contact Martin Deterre Chief Executive Officer
contact@theraclion.com
Theraclion (EU:ALTHE)
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Theraclion (EU:ALTHE)
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