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NYXH Positive Sentiment Score: 75/100

REGULATED INFORMATION Nyxoah Reports First Quarter 2024 Financial and Operating Results Announced DREAM U.S. pivotal study achieved primary endpoints On track for FDA approval as early as end of 2024 Mont-Saint-Guibert,

Key Takeaway: Nyxoah SA has reported its financial and operating results for the first quarter of 2024, highlighting significant achievements in its DREAM U.S. pivotal study which met primary endpoints. The company anticipates FDA approval for its Genio system as early as the end of 2024. Despite a substantial increase in revenue attributed to its commercialization efforts, Nyxoah continues to face operational losses. The CEO expressed optimism about future growth driven by strong clinical data and the company's innovative sleep apnea solutions.

Market Sentiment Analysis

POSITIVE FACTORS

  • Nyxoah achieved primary endpoints in the DREAM U.S. pivotal study, a significant milestone.
  • The Genio system is demonstrating promising results, highlighting its efficacy in treating OSA.
  • The company is on track for potential FDA approval by the end of 2024.
  • Revenue increased significantly in comparison to the previous year's quarter, indicating positive commercial traction.

CONCERNS & RISKS

  • Despite increased revenue, Nyxoah still reported a substantial operating loss of €12.2 million for Q1 2024.
  • The research and development expenses rose to €7.2 million, which could impact future profitability if not managed properly.

Full Press Release Details

REGULATED INFORMATION
Reports First Quarter 2024 Financial and Operating Results
U.S. pivotal study achieved primary endpoints
FDA approval as early as end of 2024
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.
and Operating Highlights
DREAM U.S. study achieving its primary endpoints is a pivotal milestone for Nyxoah and further differentiates Genio by demonstrating
similar 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."
REGULATED INFORMATION
Quarter 2024 Results
STATEMENTS OF LOSS AND OTHER COMPREHENSIVE LOSS (unaudited)
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 )
REGULATED INFORMATION
STATEMENT OF FINANCIAL POSITION (unaudited)
As at
March 31 2024 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
REGULATED INFORMATION
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.
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 Development
For 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.
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.
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.
financial report for the first quarter 2024, including details of the consolidated results, are available on the investor page of
and webcast presentation
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.
REGULATED INFORMATION
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.
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
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,
CE marked since 2019. Investigational device in the United States. Limited by U.S. federal law to investigational use in the United States.
REGULATED INFORMATION
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.
Chief Strategy Officer

Frequently Asked Questions

What major milestone did Nyxoah achieve in Q1 2024?

Nyxoah's U.S. DREAM study met its primary endpoints, a key milestone.

When could FDA approval for Genio be expected?

FDA approval for Genio could be anticipated by the end of 2024.

What is Nyxoah's primary focus?

Nyxoah focuses on innovative solutions for treating Obstructive Sleep Apnea.

How did Nyxoah's revenue change in Q1 2024?

Revenue rose to €1.22 million in Q1 2024, from €441,000 a year prior.

What was Nyxoah's gross profit margin for Q1 2024?

The gross profit margin for Q1 2024 was 62.7%.

Last updated: May 14, 2024