REGULATED INFORMATION
Nyxoah Reports First Quarter 2024
Financial and Operating ResultsAnnounced DREAM U.S.
pivotal study achieved primary endpoints On track for FDA approval
as early as end of 2024
Mont-Saint-Guibert, Belgium – May 14,
2024 10:05pm CET / 4:05pm ET – Nyxoah SA (Euronext Brussels/Nasdaq:
NYXH) (“Nyxoah” or the “Company”), a medical technology
company focused on the development and commercialization of
innovative solutions to treat Obstructive Sleep Apnea (OSA), today
reported financial and operating results for the first quarter of
2024.
Recent Financial and Operating
Highlights
- Reported the DREAM U.S. pivotal
study achieved co-primary endpoints on an intent-to-treat (ITT)
basis and demonstrated strong AHI reductions in supine and
non-supine sleep positions.
- The DREAM study achieved a median
AHI reduction of 70.8%, a 12-month AHI responder rate, per the Sher
criteria, of 63.5% (p=0.002) on an ITT basis and a 12-month ODI
responder rate of 71.3% (p<0.001) on an ITT basis.
- Preparing the fourth and final PMA
module for submission this quarter.
- Appointed Dr. Maurits S. Boon, MD
as Chief Medical Officer.
- Advanced patient access strategy
through partnership with the American Association of Otolaryngology
– Head & Neck Surgery Foundation (AAO-HNSF).
- Achieved quarterly sales of €1.2
million, showing 170% growth vs Q1 2023.
- Total cash position of €44.3
million at the end of the quarter.
“The DREAM U.S. study achieving its primary
endpoints is a pivotal milestone for Nyxoah and further
differentiates Genio as the only HGNS therapy to demonstrate strong
efficacy in supine and non-supine OSA. With the DREAM data in hand,
our U.S. launch preparations are focused on attracting commercial
talent to set us up for success when we introduce Genio,” commented
Olivier Taelman, Nyxoah Chief Executive Officer. “With continued
European commercial traction, positive DREAM data and a highly
differentiated, patient centric HGNS solution, I could not be more
excited for Nyxoah’s future.”
First Quarter 2024 Results
CONSOLIDATED STATEMENTS OF LOSS AND OTHER
COMPREHENSIVE LOSS (unaudited) (in
thousands)
|
For the three months ended March 31, |
|
2024 |
|
2023 |
Revenue |
€ 1,221 |
|
€ 441 |
Cost of goods
sold |
(455) |
|
(175) |
Gross
profit |
€ 766 |
|
€ 266 |
Research and
Development Expense |
(7,199) |
|
(6,157) |
Selling,
General and Administrative Expense |
(5,972) |
|
(5,551) |
Other
income/(expense) |
192 |
|
46 |
Operating loss for the period |
€ (12,213) |
|
€ (11,396) |
Financial
income |
1 408 |
|
625 |
Financial
expense |
( 991) |
|
( 958) |
Loss
for the period before taxes |
€ (11,796) |
|
€ (11,729) |
Income
taxes |
( 110) |
|
( 182) |
Loss
for the period |
€ (11,906) |
|
€ (11,911) |
|
|
|
|
Loss
attributable to equity holders |
€ (11,906) |
|
€ (11,911) |
|
|
|
|
Other
comprehensive income/(loss) |
|
|
|
Items
that may not be subsequently reclassified to profit or loss (net of
tax) |
|
|
|
Currency
translation differences |
60 |
|
(28) |
Total
comprehensive loss for the year, net of tax |
€ (11,846) |
|
€ (11,939) |
Loss
attributable to equity holders |
€ (11,846) |
|
€ (11,939) |
|
|
|
|
Basic loss per
share (in EUR) |
€ (0.415) |
|
€ (0.460) |
Diluted loss
per share (in EUR) |
€ (0.415) |
|
€ (0.460) |
CONSOLIDATED STATEMENT OF FINANCIAL
POSITION (unaudited)
(in thousands)
|
|
|
As at |
|
|
|
March 312024 |
|
December 31 2023 |
ASSETS |
|
|
|
|
|
Non-current assets |
|
|
|
|
|
Property,
plant and equipment |
|
|
€4,379 |
|
€4,188 |
Intangible
assets |
|
|
48,501 |
|
46,608 |
Right of use
assets |
|
|
3,597 |
|
3,788 |
Deferred tax
asset |
|
|
134 |
|
56 |
Other
long-term receivables |
|
|
1 333 |
|
1,166 |
|
|
|
€ 57,944 |
|
€ 55,806 |
Current assets |
|
|
|
|
|
Inventory |
|
|
3,418 |
|
3,315 |
Trade
receivables |
|
|
2,971 |
|
2,758 |
Other
receivables |
|
|
3,149 |
|
3,212 |
Other current
assets |
|
|
1,232 |
|
1,318 |
Financial
assets |
|
|
22,225 |
|
36,138 |
Cash and cash
equivalents |
|
|
22,077 |
|
21,610 |
|
|
|
€ 55,072 |
|
€ 68,351 |
Total assets |
|
|
€ 113,016 |
|
€ 124,157 |
|
|
|
|
|
|
EQUITY
AND LIABILITIES |
|
|
|
|
|
Capital and reserves |
|
|
|
|
|
Capital |
|
|
4,927 |
|
4,926 |
Share
premium |
|
|
246,188 |
|
246,127 |
Share based
payment reserve |
|
|
8,440 |
|
7,661 |
Other
comprehensive income |
|
|
197 |
|
137 |
Retained
loss |
|
|
(172,555) |
|
(160,829) |
Total equity attributable to shareholders |
|
|
€ 87,197 |
|
€ 98,022 |
|
|
|
|
|
|
LIABILITIES |
|
|
|
|
|
Non-current liabilities |
|
|
|
|
|
Financial
debt |
|
|
8,616 |
|
8,373 |
Lease
liability |
|
|
2,933 |
|
3,116 |
Pension
liability |
|
|
22 |
|
9 |
Provisions |
|
|
273 |
|
185 |
Deferred tax
liability |
|
|
− |
|
9 |
|
|
|
€ 11,844 |
|
€ 11,692 |
Current liabilities |
|
|
|
|
|
Financial
debt |
|
|
346 |
|
364 |
Lease
liability |
|
|
852 |
|
851 |
Trade
payables |
|
|
7,316 |
|
8,108 |
Current tax
liability |
|
|
2,091 |
|
1,988 |
Other
payables |
|
|
3,370 |
|
3,132 |
|
|
|
€ 13,975 |
|
€ 14,443 |
Total liabilities |
|
|
€ 25,819 |
|
€ 26,135 |
Total equity and liabilities |
|
|
€ 113,016 |
|
€ 124,157 |
RevenueRevenue was €1.2 million for the first
quarter ending March 31, 2024, compared to €441,000 for the first
quarter ending March 31, 2023. The increase in revenue was
attributable to the Company’s commercialization of the Genio®
system, primarily in Germany.
Cost of Goods Sold
Cost of goods sold was €455,000 for the three
months ending March 31, 2024, representing a gross profit of €0.8
million, or gross margin of 62.7%. This compares to total cost of
goods sold of €175,000 in the first quarter of 2023, for a gross
profit of €266,000, or gross margin of 60.3%.
Research and DevelopmentFor the first quarter
ending March 31, 2024, research and development expenses were €7.2
million, versus €6.2 million for the first quarter ending March 31,
2023.
Operating LossTotal operating loss for the first
quarter ending March 31, 2024 was €12.2 million versus €11.4
million in the first quarter ending March 31, 2023. This was driven
by the acceleration in the Company’s R&D spending, as well as
ongoing commercial and clinical activities.
Cash PositionAs of March 31, 2024,
cash and financial assets totaled €44.3 million, compared to €57.7
million on December 31, 2023. Total cash burn was approximately
€4.5 million per month during the first quarter 2024.
First Quarter 2024Nyxoah’s
financial report for the first quarter 2024, including details of
the consolidated results, are available on the investor page of
Nyxoah’s website (https://investors.nyxoah.com/financials).
Conference call and webcast
presentation A webcast of the call will be accessible via
the Investor Relations page of the Nyxoah website or through this
link: Nyxoah's Q1 2024 earnings call webcast. For those not
planning to ask a question of management, the Company recommends
listening via the webcast.
If you plan to ask a question, please use the
following link: Nyxoah’s Q1 2024 earnings call. After registering,
an email will be sent, including dial-in details and a unique
conference call access code required to join the live call. To
ensure you are connected prior to the beginning of the call, the
Company suggests registering a minimum of 10 minutes before the
start of the call.
About NyxoahNyxoah is a medical
technology company focused on the development and commercialization
of innovative solutions to treat Obstructive Sleep Apnea (OSA).
Nyxoah’s lead solution is the Genio® system, a patient-centered,
leadless and battery-free hypoglossal neurostimulation therapy for
OSA, the world’s most common sleep disordered breathing condition
that is associated with increased mortality risk and cardiovascular
comorbidities. Nyxoah is driven by the vision that OSA patients
should enjoy restful nights and feel enabled to live their life to
its fullest.
Following the successful completion of the BLAST
OSA study, the Genio® system received its European CE Mark in 2019.
Nyxoah completed two successful IPOs: on Euronext Brussels in
September 2020 and NASDAQ in July 2021. Following the positive
outcomes of the BETTER SLEEP study, Nyxoah received CE mark
approval for the expansion of its therapeutic indications to
Complete Concentric Collapse (CCC) patients, currently
contraindicated in competitors’ therapy. Additionally, the Company
is currently conducting the DREAM IDE pivotal study for FDA and US
commercialization approval.
For more information, please visit
http://www.nyxoah.com/.
Caution – CE marked since 2019.
Investigational device in the United States. Limited by U.S.
federal law to investigational use in the United States.
Forward-looking statements Certain
statements, beliefs and opinions in this press release are
forward-looking, which reflect the Company's or, as appropriate,
the Company directors' or managements' current expectations
regarding the Genio® system; planned and ongoing clinical studies
of the Genio® system; the potential advantages of the Genio®
system; Nyxoah’s goals with respect to the development, regulatory
pathway and potential use of the Genio® system; the utility of
clinical data in potentially obtaining FDA approval of the Genio®
system; and the Company's results of operations, financial
condition, liquidity, performance, prospects, growth and
strategies. By their nature, forward-looking statements involve a
number of risks, uncertainties, assumptions and other factors that
could cause actual results or events to differ materially from
those expressed or implied by the forward-looking statements. These
risks, uncertainties, assumptions and factors could adversely
affect the outcome and financial effects of the plans and events
described herein. Additionally, these risks and uncertainties
include, but are not limited to, the risks and uncertainties set
forth in the “Risk Factors” section of the Company’s Annual Report
on Form 20-F for the year ended December 31, 2023, filed with the
Securities and Exchange Commission (“SEC”) on March 20, 2024, and
subsequent reports that the Company files with the SEC. A multitude
of factors including, but not limited to, changes in demand,
competition and technology, can cause actual events, performance or
results to differ significantly from any anticipated development.
Forward looking statements contained in this press release
regarding past trends or activities are not guarantees of future
performance and should not be taken as a representation that such
trends or activities will continue in the future. In addition, even
if actual results or developments are consistent with the
forward-looking statements contained in this press release, those
results or developments may not be indicative of results or
developments in future periods. No representations and warranties
are made as to the accuracy or fairness of such forward-looking
statements. As a result, the Company expressly disclaims any
obligation or undertaking to release any updates or revisions to
any forward-looking statements in this press release as a result of
any change in expectations or any change in events, conditions,
assumptions or circumstances on which these forward-looking
statements are based, except if specifically required to do so by
law or regulation. Neither the Company nor its advisers or
representatives nor any of its subsidiary undertakings or any such
person's officers or employees guarantees that the assumptions
underlying such forward-looking statements are free from errors nor
does either accept any responsibility for the future accuracy of
the forward-looking statements contained in this press release or
the actual occurrence of the forecasted developments. You should
not place undue reliance on forward-looking statements, which speak
only as of the date of this press release.
Contacts:NyxoahDavid DeMartino,
Chief Strategy OfficerIR@nyxoah.com
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