Recent Updates
Recently added Catalysts
NYXH Positive Sentiment Score: 70/100

REGULATED INFORMATION Nyxoah Reports Third Quarter Financial and Operating Results FDA approval on track for first quarter 2025, U.S. commercial team build out in progress Company fully funded with cash until mid 2026 Mo

Key Takeaway: Nyxoah SA reported its third quarter financial results, indicating a revenue increase to €1.3 million, up from €1.0 million a year earlier. The company is on track for FDA approval of its Genio system in Q1 2025 and is expanding its U.S. commercial team. However, it faced an operating loss of €15 million, driven by increased R&D and other operational expenses. Despite these challenges, Nyxoah is fully funded through mid-2026, suggesting strong financial support for its ongoing projects.

Market Sentiment Analysis

POSITIVE FACTORS

  • FDA approval for the Genio system is on track for Q1 2025.
  • The company has successfully raised additional capital and is building its U.S. commercial team.
  • Nyxoah reported increased revenue for Q3 2024 compared to the same quarter in 2023.
  • The ongoing clinical activities and positive study outcomes enhance the company's market position.

CONCERNS & RISKS

  • The company experienced a significant operating loss of €15 million in Q3 2024, an increase from the previous year.
  • R&D expenses are rising, indicating increased financial pressure.
  • Despite a rise in revenue, overall financial performance remains negative due to high operational costs.
  • The reliance on the success of upcoming regulatory approvals creates uncertainty.

Full Press Release Details

Reports Third Quarter Financial and Operating Results
approval on track for first quarter 2025, U.S. commercial team build out in progress
fully funded with cash until mid 2026
Belgium - November 6, 2024, 10:05pm CET / 4:05pm ET - Nyxoah SA (Euronext Brussels/Nasdaq: NYXH) ("Nyxoah"
or the "Company"), a medical technology company that develops breakthrough treatment alternatives for Obstructive Sleep Apnea
(OSA) through neuromodulation, today reported financial and operating results for the third quarter of 2024.
Recent Financial and Operating Highlights
"Our actions in the third
quarter have further positioned us well for a successful U.S. commercial launch. On the back of the robust DREAM data presented in September,
we have raised additional capital and are actively focused on building up our U.S. commercial team," commented Olivier Taelman,
Nyxoah's Chief Executive Officer. "I am more confident than ever that we have set Genio up for a strong commercial start in
the U.S. immediately after FDA approval."
Third Quarter 2024 Results
CONSOLIDATED STATEMENTS OF LOSS
AND OTHER COMPREHENSIVE LOSS (unaudited)
For the three months ended September 30, For the nine months ended September 30,
2024 2023 2024 2023
Revenue 1,266 976 3,258 2,524
Cost of goods sold (482 ) (336 ) (1,217 ) (930 )
Gross profit 784 640 2,041 1,594
Research and Development Expense (7,902 ) (6,568 ) (22,573 ) (19,330 )
Selling, General and Administrative Expense (8,042 ) (5 058) (20,396 ) (16,794 )
Other income/(expense) 180 - 430 265
Operating loss for the period (14,980 ) (10,986 ) (40,498 ) (34,265 )
Financial income 1,138 2,178 4,615 3,592
Financial expense (3,043 ) (1,033 ) (5,480 ) (2,765 )
Loss for the period before taxes (16,885 ) (9,841 ) (41,363 ) (33,438 )
Income taxes (173 ) 2,229 (724 ) 1,119
Loss for the period (17,058 ) (7,612 ) (42,087 ) (32,319 )
Loss attributable to equity holders (17,058 ) (7,612 ) (42,087 ) (32,319 )
Other comprehensive income/(loss)
Items that may not be subsequently reclassified to profit or loss (net of tax)
Currency translation differences (209 ) (10 ) (221 ) (88 )
Total comprehensive loss for the year, net of tax (17,267 ) (7,622 ) (42,308 ) (32,407 )
Loss attributable to equity holders (17,267 ) (7,622 ) (42,308 ) (32,407 )
Basic loss per share (in EUR) (0.496 ) (0.266 ) (1.346 ) (1.166 )
Diluted loss per share (in EUR) (0.496 ) (0.266 ) (1.346 ) (1.166 )
CONSOLIDATED STATEMENT
OF FINANCIAL POSITION (unaudited)
As at
September 30, 2024 December 31, 2023
ASSETS
Non-current assets
Property, plant and equipment 4,461 4,188
Intangible assets 49,558 46,608
Right of use assets 3,635 3,788
Deferred tax asset 53 56
Other long-term receivables 1,475 1,166
59,182 55,806
Current assets
Inventory 5,272 3,315
Trade receivables 2,504 2,758
Other receivables 2,992 3,212
Other current assets 1,837 1,318
Financial assets 42,299 36,138
Cash and cash equivalents 28,678 21,610
83,582 68,351
Total assets 142,764 124,157
EQUITY AND LIABILITIES
Capital and reserves
Capital 5,908 4,926
Share premium 290,906 246,127
Share based payment reserve 8,943 7,661
Other comprehensive income (84 ) 137
Retained loss (200,966 ) (160,829 )
Total equity attributable to shareholders 104,707 98,022
LIABILITIES
Non-current liabilities
Financial debt 19,143 8,373
Lease liability 2,636 3,116
Pension liability 47 9
Provisions 398 185
Deferred tax liability 12 9
22,236 11,692
Current liabilities
Financial debt 399 364
Lease liability 1,151 851
Trade payables 7,109 8,108
Current tax liability 2,495 1,988
Other payables 4,667 3,132
15,821 14,443
Total liabilities 38,057 26,135
Total equity and liabilities 142,764 124,157
Revenue was 1.3 million for the third quarter
ending September 30, 2024, compared to 1.0 million for the third quarter ending September 30, 2023.
Cost of goods sold was 482,000 for the three
months ending September 30, 2024, representing a gross profit of 0.8 million, or gross margin of 62.0%. This compares to total cost
of goods sold of 336,000 in the third quarter of 2023, for a gross profit of 0.6 million, or gross margin of 66.0%.
Research and Development
For the third quarter ending September 30, 2024,
research and development expenses were 7.9 million, versus 6.6 million for the third quarter ending September 30, 2023.
Total operating loss for the third quarter ending
September 30, 2024, was 15.0 million versus 11.0 million in the third quarter ending September 30, 2023. This increase was
primarily driven by expanded commercial activities, higher R&D investments, and ongoing clinical activities.
As of September 30, 2024, cash and financial assets
totaled 71.0 million, compared to 57.7 million on December 31, 2023. Total cash burn was approximately 5.6 million per
month during the third quarter 2024.
Nyxoah's financial report for the third
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
Company management will host a conference call
to discuss financial results on Wednesday, November 6, 2024, beginning at 10:30pm CET / 4:30pm ET.
A webcast of the call will be accessible via
the Investor Relations page of the Nyxoah website or through this link: Nyxoah's Q3 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 Q3 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.
The archived webcast will be available for replay
shortly after the close of the call.
Nyxoah is reinventing sleep for the billion people
that suffer from obstructive sleep apnea (OSA). We are a medical technology company that develops breakthrough treatment alternatives
for OSA through neuromodulation. Our first innovation is Genio , a battery-free hypoglossal neuromodulation device that is inserted
through a single incision under the chin and controlled by a wearable. Through our commitment to innovation and clinical evidence, we
have shown best-in-class outcomes for reducing OSA burden.
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 announced positive outcomes from the DREAM IDE pivotal study for FDA and U.S. commercialization approval.
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 reporting
data from Nyxoah's DREAM U.S. pivotal trial; receipt of FDA approval; entrance to the U.S. market; and the anticipated closing
and use of the proceeds from the offering. 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.
This press release does not constitute an offer
to sell or a solicitation of an offer to buy the securities in the offering, nor shall there be any sale of these securities in any jurisdiction
in which an offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of such jurisdiction.
FINN Partners - Glenn Silver
Backstage Communication - Gunther De Backer
In International/Germany
MC Services - Anne Hennecke

Frequently Asked Questions

When is the FDA approval for Genio expected?

FDA approval for Genio is anticipated in the first quarter of 2025.

How much cash does Nyxoah have until mid-2026?

Nyxoah is fully funded with cash available until mid-2026.

What was Nyxoah's revenue for Q3 2024?

Nyxoah reported a revenue of €1.3 million for Q3 2024.

What was the loss for Nyxoah in Q3 2024?

Nyxoah reported a loss of €17.1 million for the third quarter of 2024.

What device does Nyxoah develop for OSA?

Nyxoah develops Genio, a battery-free neuromodulation device for OSA.

Last updated: Nov 6, 2024