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Gravity Anunciou Lançamento Oficial da Aventura de Quebra-cabeças Fofos e Sombrios “PIGROMANCE” no Steam!

– Táticas e Criatividade Premiadas em Todo o Mundo
– Lançamento Oficial com 20% de Desconto

SEUL, Coreia do Sul, July 25, 2024 (GLOBE NEWSWIRE) — A desenvolvedora e editora global de jogos Gravity anunciou o lançamento oficial da aventura de quebra–cabeças “PIGROMANCE” no Steam em 25 de julho.

A aventura de quebra–cabeça “PIGROMANCE” elabora a história de um porco nascido com o destino de se tornar uma salsicha, escapando de uma fábrica de salsichas para encontrar seu amor. Os jogadores podem resolver quebra–cabeças enquanto escapam do Cuttingman e navegam pelos obstáculos perigosos ocultos na fábrica de salsichas. “PIGROMANCE” tem gráficos chibi fofos com vibrações contrastantes de iluminação escura, efeitos visuais e sonoros horripilantes e BGMs assustadores que quase se assemelham a contos de fadas perturbadores.

Mesmo antes do seu lançamento oficial, o “PIGROMANCE” foi reconhecido por sua notável estratégia e novo conceito ao ganhar vários prêmios, incluindo o Prêmio de Excelência no 2024 INDIE CRAFT, MWU(Made With Unity) KR 2023 “Melhor Indie” Categoria, 1º lugar no 2022 Level Up Showcase, 2º lugar no 2022 G–STAR Indie Awards e Silver Award no Global Indie Game Development Contest 2020. “PIGROMANCE” foi elogiado em vários eventos de jogos por sua nova narrativa e suspense em desenvolvimento.

A versão oficial de lançamento agora está disponível para jogar no Steam com suporte para 9 idiomas diferentes, incluindo coreano, inglês, japonês, chinês simplificado e francês. A Gravity está oferecendo um desconto de 20% até 7 de agosto para comemorar o lançamento oficial.

“O “PIGROMANCE” é um jogo com estratégia comprovada com os vários prêmios de jogos recebidos, que recebeu comentários positivos e ganhou uma reputação positiva dos jogadores no local. Qualquer pessoa, incluindo jogadores que preferem jogos casuais, pode jogar o “PIGROMANCE””, disse Yoo Jun, gerente principal do departamento de negócios de jogos de console da Gravity. “Elevamos o nível de conclusão do jogo, de acordo com o feedback inestimável dos jogadores, e o jogo apresenta estilos de arte e histórias cativantes que serão bastante diferentes de muitos outros jogos casuais. Agradecemos a todos os jogadores que aguardam o lançamento oficial.”

[Página oficial da Gravity] http://www.gravity.co.kr
[Página oficial da Steam Store do PIGROMANCE] https://store.steampowered.com/app/1362120/_/
[Página oficial do PIGROMANCE] https://www.pigromance.com/default/

– Perguntas: Unidade de negócios Gravity 2
Parque Sang–min/ smpark@gravity.co.kr

Foto deste comunicado disponível em https://www.globenewswire.com/NewsRoom/AttachmentNg/75b67025–4d30–468e–818f–4a91a0c28633


GLOBENEWSWIRE (Distribution ID 9193298)

PDF Solutions signs a Sales Representative Agreement with ADMATI Agencies

SANTA CLARA, Calif., July 24, 2024 (GLOBE NEWSWIRE) — PDF Solutions, Inc. (Nasdaq: PDFS), a leading provider of comprehensive data solutions for the semiconductor and electronics ecosystems, today announced a formal agreement with ADMATI Agencies Ltd. as a Sales Representative for PDF Solutions throughout Israel.

With this agreement Admati Agencies will promote, sell and distribute all of PDF Solutions Exensio products in the Israel market. The Exensio Analytics platform is designed and architected to meet the needs and requirements in semiconductor manufacturing from new product introduction to high volume manufacturing. Whether you are a fabless, IDM or foundry or taking on COT initiatives, Exensio has a rich set of applications to meet your needs (TTM, quality, reliability, etc.). Israel is a country with a very active semiconductor ecosystem and the Admati Agencies will be instrumental in PDF Solutions’ ability to further penetrate this growing market.

Admati Agencies (www.admati.com) is an independent engineering services and manufacturer’s representative company led by its founder Udi Admati. Based in Haifa, Admati Agencies has been representing technology principals since 2007. They support customers across various industries including medical, automotive, defense, semiconductor, telecommunications, vehicle, agriculture and industrial durable goods.

“We are looking forward to leverage Admati Agencies’ deep connections within the technology industry sector in Israel. This agreement is a key step to further our market positioning in this part of the world,” says, Peter Szalay, Vice President, business development, PDF Solutions. “Their reputation and support structure are a perfect fit for PDF Solutions.”

About ADMATI Agencies
Since 2007 Admati Agencies has shown exceptional growth, due to our commitment to set the industry service standard for excellence. Admati started as a technical services house for the semi–conductor industry. The company established itself as a leading provider of maintenance of back–end equipment and expanded into supplying back–end hardware, test sockets, burning sockets, probes, etc. Today, Admati is a leading provider of sockets, pins, ICT pins, connectors and flex–PCB to many of the largest brands in the Israeli market. In addition, we provide production engineering and outsourcing services to companies that would like to move their production to South–East Asia. We service the Medical, Military, Industrial, and Semiconductor Industries.

For more information please visit:
mpi–corporation.com
or
admati.com

About PDF Solutions
PDF Solutions (Nasdaq: PDFS) provides comprehensive data solutions designed to empower organizations across the semiconductor and electronics ecosystems to improve the yield and quality of their products and operational efficiency for increased profitability. The Company’s products and services are used by Fortune 500 companies across the semiconductor ecosystem to achieve smart manufacturing goals by connecting and controlling equipment, collecting data generated during manufacturing and test operations, and performing advanced analytics and machine learning to enable profitable, high–volume manufacturing.

Founded in 1991, PDF Solutions is headquartered in Santa Clara, California, with operations across North America, Europe, and Asia. The Company (directly or through one or more subsidiaries) is an active member of SEMI, INEMI, TPCA, IPC, the OPC Foundation, and DMDII. For the latest news and information about PDF Solutions or to find office locations, visit https://www.pdf.com/.

PDF Solutions, the PDF Solutions logo, and Exensio are trademarks or registered trademarks of PDF Solutions, Inc. or its subsidiaries.

Company Contacts
Christophe Begue
VP, Corporate Strategic Marketing
(408) 938–6408
christophe.begue@pdf.com

Sonia Segovia
Investor Relations
(408) 938–6491
sonia.segovia@pdf.com


GLOBENEWSWIRE (Distribution ID 9192293)

DigiAsia Corp. Announces YoY Transaction Volume Growth of 74% Keeping with its Strong Growth Trajectory

NEW YORK, July 23, 2024 (GLOBE NEWSWIRE) — DigiAsia Corp. (NASDAQ: FAAS) (“DigiAsia” or the “Company”), a leading Fintech as a Service (“FaaS”) ecosystem provider, today announced key growth highlights of the following KPIs:

  • 7.85 billion transactions¹ for the full year 2023, compared to 4.1 billion transactions in the first half of 2023 and 4.5 billion transactions during the full year 2022
  • $3.625 billion gross transaction value for the full year 2023, compared to $1.6 billion in the first half of 2023 and $2.1 billion gross transaction value in the full year 2022
  • 1 million total merchants on the platform, growth of 31.5%, compared to 760,100 merchants at the end of 2022
  • 40% increase in Enterprise Payment and Banking Partners on the platform, up significantly compared to 48 customers in 2022

Forward–Looking Statements:

This press release may contain forward–looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. The words “believe”, “expect”, “anticipate”, “project”, “targets”, “optimistic”, “confident that”, “continue to”, “predict”, “intend”, “aim”, “will” or similar expressions are intended to identify forward–looking statements. All statements other than statements of historical fact are statements that may be deemed forward–looking statements. These forward–looking statements including, but not limited to, statements concerning DigiAsia and the Company’s operations, financial performance and condition are based on current expectations, beliefs and assumptions which are subject to change at any time. DigiAsia cautions that these statements by their nature involve risks and uncertainties, and actual results may differ materially depending on a variety of important factors such as government and stock exchange regulations, competition, political, economic and social conditions around the world including those discussed in DigiAsia’s Form 20–F under the headings “Risk Factors”, “Management’s Discussion and Analysis of Financial Condition and Results of Operations” and “Business Overview” and other reports filed with the Securities and Exchange Commission from time to time. All forward–looking statements are applicable only as of the date it is made and DigiAsia specifically disclaims any obligation to maintain or update the forward–looking information, whether of the nature contained in this release or otherwise, in the future.

DigiAsia Company Contact:
Subir Lohani
Chief Financial Officer and Chief Strategy Officer
646–480–0142

Investor Contact:
MZ North America
Email: FAAS@mzgroup.us

_____________

¹ Includes # of API hits


GLOBENEWSWIRE (Distribution ID 9192038)

Cellebrite Advances Plans to Transform and Elevate its Strategic Relationship with the U.S. Federal Government

TYSONS CORNER, Va. and PETAH TIKVA, Israel, July 17, 2024 (GLOBE NEWSWIRE) — Cellebrite (NASDAQ: CLBT), a leader in digital investigative solutions for the public and private sectors, officially established Cellebrite Federal Solutions, further elevating the Company’s ability to serve the unique needs of the U.S. federal government through its AI–driven Case–to–Closure [C2C] platform for accelerating justice. 

This newly established operation builds on the Company's long and rich history of serving U.S. justice, defense, intelligence and other federal civilian agencies with its world–renowned Case–to–Closure platform, assisting in critical initiatives targeting the safety and protection of all American citizens.

A key element of this announcement is the acquisition of Cyber Technology Services, Inc. (CyTech). CyTech, which was founded in 2002, brings extensive domain expertise in cybersecurity, digital forensics and incident response services. CyTech’s employees will be part of Cellebrite Federal Solutions, further broadening and complementing Cellebrite's capabilities and supporting the Company’s ongoing expansion within this customer segment.

The actions announced by Cellebrite today support the Company’s strategy to substantially broaden its business with U.S. federal customers over the longer term. Terms of the transaction were not disclosed.

“The establishment of this dedicated unit underscores Cellebrite’s strategic commitment to the federal sector, recognizing its critical role and potential in our mission to enhance public safety and accelerate justice,” said Tom Hogan, Cellebrite Executive Chairman of the Board. “Today’s actions, combined with the investments we are making to achieve FedRAMP authorization of our software–as–a–service offerings, demonstrate that Cellebrite is taking strategic steps to address the evolving needs of our U.S. federal customers and unlock more opportunity with them over the coming years.”

“This is an exciting venture, and we welcome this talented group to our team,” said Yossi Carmil, Cellebrite’s CEO. “This move reinforces our dedication and support for the U.S. federal government to have the best digital investigative resources.”

The new unit will be led by Erik Sachwitz. Erik has led Cellebrite's U.S. federal business since 2020. In 2023, U.S. federal customers generated approximately 19% of Cellebrite’s annual recurring revenue in the public sector, up 21% from the prior year. Erik brings a rich history of software expertise to the public sector including stints at Quest Software, Micro Focus and Attachmate. 

“This is a game–changing opportunity for CyTech, and we are thrilled to join Cellebrite to better engage these unique partnerships with the U.S. federal government,” said Tim Poole, formerly President of CyTech who now serves as Vice President of Cellebrite Federal Solutions. “As a seasoned digital forensics professional, I know first–hand what our customers are dealing with. We are here to strengthen the incredible offerings from Cellebrite that will help our U.S. federal customers achieve their objectives.”

Further, Cellebrite Federal Solutions is building a world–class board of independent directors. These directors bring a wealth of expertise and a range of valued skills covering U.S. defense, cyber intelligence, SaaS and cloud execution and prosecutorial expertise. 

The four independent directors are:

  • Lt. Gen. (ret.) Ken Tovo: former Commander of the Green Berets and U.S. Special Forces
    • Ken, a distinguished leader in special operations and strategic planning, has a 35–year career that spans from Green Beret service to leading the 34,000–strong Army Special Operations Command. Ken currently serves on the boards of several companies, is the chairman of the Green Beret Foundation, a non–profit organization dedicated to assisting US Army Green Berets and their families and is an advisory board member of a nonprofit that supports the educational needs of killed, wounded or seriously injured servicemembers. Ken is the president of DOL Enterprises, Inc, a consulting firm providing services primarily in the defense and technology sectors.
  • Dr. Barry West: former CIO and CISO U.S. Department of Commerce and Department of Homeland Security
    • Dr. West is a veteran technologist and business leader with over 40 years of experience in the information technology field, and his expertise spans areas such as cybersecurity, cloud computing and innovation. Dr. West’s experience includes serving as CIO at the FDIC, PBGC, DOC, FEMA, NWS and DHS. Currently, he serves as the Founder and CEO of West Wing Advisory Services, LLC.
  • Mark Ferrer: former COO of SAP
    • Mark is an experienced global operating executive, currently serving on the board of directors for Blue Ridge Networks and Vbrick Corp. His extensive background includes leadership roles at Citrix, SAP, HP, and pivotal CEO positions at two public companies, contributing to significant market cap growth and strategic initiatives in the technology industry.
  • Barbara Grewe: Sr. Director FBI 9/11 Review Commission
    • Barbara is a seasoned professional with a diverse background in international strategy, policy and cybersecurity, having held senior roles at The MITRE Corporation, FBI 9/11 Review Commission and the Government Accountability Office. Her extensive experience spans from strategic management consulting at McKinsey & Co. and litigation at Covington & Burling, to serving as an Assistant U.S. Attorney, demonstrating her versatility and commitment to public service.

About Cellebrite
Cellebrite’s (Nasdaq: CLBT) mission is to enable its customers to protect and save lives, accelerate justice and preserve privacy in communities around the world. We are a global leader in Digital Investigative solutions for the public and private sectors, empowering organizations in mastering the complexities of legally sanctioned digital investigations by streamlining intelligence processes. Trusted by thousands of leading agencies and companies worldwide, Cellebrite’s Digital Investigative platform and solutions transform how customers collect, review, analyze and manage data in legally sanctioned investigations. To learn more visit us at www.cellebrite.com, https://investors.cellebrite.com, or follow us on X at @Cellebrite.

Caution Regarding Forward Looking Statements
This document includes “forward–looking statements” within the meaning of the “safe harbor” provisions of the United States Private Securities Litigation Reform Act of 1995. Forward looking statements may be identified by the use of words such as “forecast,” “intend,” “seek,” “target,” “anticipate,” “will,” “appear,” “approximate,” “foresee,” “might,” “possible,” “potential,” “believe,” “could,” “predict,” “should,” “continue,” “expect,” “estimate,” “may,” “plan,” “outlook,” “future” and “project” and other similar expressions that predict, project or indicate future events or trends or that are not statements of historical matters. Such forward–looking statements include, but are not limited to, the following: CyTech’s employees will be part of Cellebrite Federal Solutions, further broadening and complementing Cellebrite's capabilities and supporting the Company’s ongoing expansion within this customer segment; with the boost of talents from CyTech, we are even better positioned to serve our federal partners and support their missions; and today’s actions, combined with the investments we are making to achieve FedRAMP authorization of our software–as–a–service offerings, demonstrate that Cellebrite is taking strategic steps to address the evolving needs of our U.S. federal government agency customers and unlock more opportunity with them over the coming years. Such forward–looking statements are based on current expectations that are subject to risks and uncertainties. A number of factors could cause actual results or outcomes to differ materially from those indicated by such forward–looking statements. These factors include, but are not limited to: Cellebrite’s ability to keep pace with technological advances and evolving industry standards; Cellebrite’s material dependence on the purchase, acceptance and use of its solutions by law enforcement and government agencies; real or perceived errors, failures, defects or bugs in Cellebrite’s solutions; Cellebrite’s failure to maintain the productivity of sales and marketing personnel, including relating to hiring, integrating and retaining personnel; intense competition in all of Cellebrite’s markets; the inadvertent or deliberate misuse of Cellebrite’s solutions; failure to manage its growth effectively; Cellebrite’s ability to introduce new solutions and add–ons; its dependency on its customers renewing their subscriptions; the low volume of business Cellebrite conducts via e–commerce; risks associated with the use of artificial intelligence; the risk of requiring additional capital to support the growth of its business; risks associated with higher costs or unavailability of materials used to create its hardware product components; fluctuations in foreign currency exchange rates; lengthy sales cycle for some of Cellebrite’s solutions; near term declines in new or renewed agreements; risks associated with inability to retain qualified personnel and senior management; the security of Cellebrite’s operations and the integrity of its software solutions; risks associated with the negative publicity related to Cellebrite’s business and use of its products; risks related to Cellebrite’s intellectual property; the regulatory constraints to which Cellebrite is subject; risks associated with Cellebrite’s operations in Israel, including the ongoing Israel–Hamas war and the risk of a greater regional conflict; risks associated with different corporate governance requirements applicable to Israeli companies and risks associated with being a foreign private issuer and an emerging growth company; market volatility in the price of Cellebrite’s shares; changing tax laws and regulations; risks associated with joint ventures, partnerships and strategic initiatives; risks associated with Cellebrite’s significant international operations; risks associated with Cellebrite’s failure to comply with anti–corruption, trade compliance, anti–money–laundering and economic sanctions laws and regulations; risks relating to the adequacy of Cellebrite’s existing systems, processes, policies, procedures, internal controls and personnel for Cellebrite’s current and future operations and reporting needs; and other factors, risks and uncertainties set forth in the section titled “Risk Factors” in Cellebrite’s annual report on Form 20–F filed with the SEC on March 21, 2024 and as amended on April 12, 2024, and in other documents filed by Cellebrite with the U.S. Securities and Exchange Commission (“SEC”), which are available free of charge at www.sec.gov. You are cautioned not to place undue reliance upon any forward–looking statements, which speak only as of the date made, in this communication or elsewhere. Cellebrite undertakes no obligation to update its forward–looking statements, whether as a result of new information, future developments or otherwise, should circumstances change, except as otherwise required by securities and other applicable laws.

Contacts:

Media
Victor Cooper
Sr. Director of Corporate Communications + Content Operations
Victor.cooper@cellebrite.com 
+1 404.804.5910

Investors
Andrew Kramer
Vice President, Investor Relations
investors@cellebrite.com 
+1 973.206.7760 


GLOBENEWSWIRE (Distribution ID 9179020)

Nyxoah Nomme Scott Holstine Chief Commercial Officer

Nyxoah Nomme Scott Holstine Chief Commercial Officer

Mont–Saint–Guibert, Belgique – 15 juillet 2024, 8h00 CET / 2h00 ET – Nyxoah SA (Euronext Brussels/ Nasdaq : NYXH) (“Nyxoah” ou la “Société”) opère dans le secteur des technologies médicales et se concentre sur le développement et la commercialisation de solutions innovantes destinées à traiter le Syndrome d’Apnées Obstructives du Sommeil (SAOS). La Société a annoncé la nomination de Scott Holstine au poste de Chief Commercial Officer. À ce titre, Scott dirigera les opérations commerciales de Nyxoah afin d'assurer le succès du lancement aux États–Unis.

Scott apporte plus de 26 ans d'expérience dans l'industrie des dispositifs médicaux, avec une expérience reconnue dans le lancement de produits aux États–Unis, la mise en place et la direction d'organisations commerciales caractérisées par une forte exécution opérationnelle. Scott est un fervent avocat du développement des personnes et des talents. Scott a été lauréat du Superintendent's Award for Excellence (Star Wreath) de la United States Military Academy de West Point, à New York. Après avoir servi comme capitaine dans la U.S. Army, Scott a obtenu son MBA à l'Université du Minnesota, Carlson School of Management – Minneapolis, MN.

“Alors que nous attendons l'approbation de la FDA d'ici la fin de l'année 2024, le recrutement d'un leader commercial expérimenté est déterminant pour accélérer davantage notre stratégie de mise sur le marché aux États–Unis dans un plan d'exécution de lancement concret. Cela commence par la mise en place d'une équipe commerciale pleinement opérationnelle d'ici la fin de l'année. Scott est un leader dynamique et créatif qui a su développer des équipes performantes et de nouveaux marchés pour des technologies innovantes”, a commenté Olivier Taelman, CEO de Nyxoah. “Cette nomination marque le coup d'envoi de la constitution d'une équipe de professionnels de classe mondiale, centrée sur les patients et les cliniciens, soutenant la mission de Nyxoah qui consiste à rendre le sommeil à nouveau simple pour les patients souffrant de SAOS.”

“C'est une période prometteuse pour les patients souffrant de SAOS. Les excellents résultats de l'étude DREAM de Nyxoah et le succès de Genio sur les marchés en dehors des États–Unis ont démontré le potentiel de la solution unique et révolutionnaire de Genio. Les patients et les médecins attendent avec impatience l'arrivée d'un deuxième acteur dans le domaine du HGNS. Je suis ravi de faire partie de l'équipe qui met en place une opération commerciale axée sur le patient et qui donne la priorité à la réussite de nos partenaires fournisseurs de soins de santé dans le traitement du SAOS”, a ajouté Scott.

A propos de Nyxoah

Nyxoah opère dans le secteur des technologies médicales. Elle se concentre sur le développement et la commercialisation de solutions innovantes destinées à traiter le Syndrome d’Apnées Obstructives du Sommeil (SAOS). La principale solution de Nyxoah est le système Genio®, une thérapie de neurostimulation du nerf hypoglosse sans sonde et sans batterie qui a reçu le marquage CE, centrée sur le patient et destinée à traiter le Syndrome d’Apnées Obstructives du Sommeil (SAOS), le trouble respiratoire du sommeil le plus courant au monde. Ce dernier est associé à un risque accru de mortalité et des comorbidités, dont les maladies cardiovasculaires. La vision de Nyxoah est que les patients souffrant de SAOS doivent pouvoir profiter de nuits réparatrices et vivre pleinement leur vie.

À la suite de la réussite de l'étude BLAST OSA, le système Genio® a reçu son marquage CE européen en 2019. Nyxoah a réalisé deux introductions en bourse réussies : sur Euronext Bruxelles en septembre 2020 et sur le NASDAQ en juillet 2021. Suite aux résultats positifs de l'étude BETTER SLEEP, Nyxoah a reçu l'approbation du marquage CE pour l'élargissement de ses indications thérapeutiques aux patients atteints de Collapse Concentrique Complet (CCC), actuellement contre–indiqués dans la thérapie des concurrents. En outre, la Société mène actuellement l'étude pivot DREAM IDE en vue d'obtenir l'approbation FDA et de commercialisation aux États–Unis.

Pour plus d'informations, veuillez consulter le rapport annuel de la société pour l'exercice 2023 et visiter le site suivant http://www.nyxoah.com/.

Attention – Marquage CE depuis 2019. Dispositif expérimental aux États–Unis. Limité par la loi fédérale américaine à un usage expérimental aux États–Unis.

Déclarations Prospectives

Certaines déclarations, croyances et opinions contenues dans le présent communiqué de presse sont de nature prospective et reflètent les attentes actuelles de la société ou, le cas échéant, des administrateurs ou de la direction de la société concernant la conclusion de l'accord de facilité de prêt et de l'accord de bons de souscription synthétiques avec la BEI, l'utilisation du produit de l'accord de facilité de prêt ; le système Genio® et les études cliniques en cours sur le système Genio® ; les avantages potentiels du système Genio® ; les objectifs de Nyxoah concernant le développement, la voie réglementaire et l'utilisation potentielle du système Genio® ; l'utilité des données cliniques pour l'obtention éventuelle de l'approbation de la FDA pour le système Genio® ; la communication des données de l'essai pivot DREAM U. U. de Nyxoah, le dépôt d'une demande d'approbation auprès de la FDA et l'entrée sur le marché américain. De par leur nature, les déclarations prospectives impliquent un certain nombre de risques, d'incertitudes, d'hypothèses et d'autres facteurs susceptibles d'entraîner une différence matérielle entre les résultats ou événements réels et ceux exprimés ou sous–entendus dans les déclarations prospectives. Ces risques, incertitudes, hypothèses et facteurs pourraient avoir une incidence négative sur les résultats et les effets financiers des plans et des événements décrits dans le présent document. En outre, ces risques et incertitudes comprennent, sans s'y limiter, les risques et incertitudes énoncés dans la section “Facteurs de risque” du rapport annuel de la société sur le formulaire 20–F pour l'exercice clos le 31 décembre 2023, déposé auprès de la Securities and Exchange Commission (“SEC”) le 20 mars 2024, et des rapports ultérieurs que la société dépose auprès de la SEC. Une multitude de facteurs, y compris, mais sans s'y limiter, les changements dans la demande, la concurrence et la technologie, peuvent faire en sorte que les événements, les performances ou les résultats réels diffèrent de manière significative de tout développement anticipé. Les déclarations prospectives contenues dans le présent communiqué de presse concernant des tendances ou des activités passées ne constituent pas des garanties de performances futures et ne doivent pas être considérées comme une déclaration selon laquelle ces tendances ou activités se poursuivront à l'avenir. En outre, même si les résultats ou développements réels sont conformes aux déclarations prospectives contenues dans le présent communiqué de presse, ces résultats ou développements peuvent ne pas être représentatifs des résultats ou développements des périodes futures. Aucune déclaration ou garantie n'est donnée quant à l'exactitude ou à la justesse de ces déclarations prévisionnelles. En conséquence, la Société décline expressément toute obligation ou tout engagement de publier des mises à jour ou des révisions des déclarations prospectives contenues dans le présent communiqué de presse à la suite d'un changement des attentes ou d'un changement des événements, conditions, hypothèses ou circonstances sur lesquels ces déclarations prospectives sont basées, sauf si la loi ou la réglementation l'exige expressément. Ni la Société, ni ses conseillers ou représentants, ni aucune de ses filiales, ni les dirigeants ou employés de ces personnes ne garantissent que les hypothèses sous–jacentes à ces déclarations prospectives sont exemptes d'erreurs et n'acceptent aucune responsabilité quant à l'exactitude future des déclarations prospectives contenues dans ce communiqué de presse ou quant à la survenance effective des développements prévus. Vous ne devriez pas accorder une confiance excessive aux déclarations prospectives, qui ne sont valables qu'à la date du présent communiqué de presse.

Contact :

Nyxoah
David DeMartino, Chief Strategy Officer
IR@nyxoah.com

Media
Belgique / France
Backstage Communication – Gunther De Backer
gunther@backstagecom.be

International/ Allemagne
MC Services – Anne Hennecke
anne.hennecke@mc–services.eu

Pièce jointe


GLOBENEWSWIRE (Distribution ID 1000971439)

Nyxoah Appoints Scott Holstine as Chief Commercial Officer

Nyxoah Appoints Scott Holstine as Chief Commercial Officer

Mont–Saint–Guibert, Belgium – July 15, 2024, 8:00am CET / 2:00am 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 announced the appointment of Scott Holstine as Chief Commercial Officer. In this role, Scott will lead the commercial operations of Nyxoah enabling a successful U.S. launch.

Scott brings over 26 years of experience in the medical device industry with a proven track record in U.S. product launches, building and leading commercial organizations trademarked by strong operational execution. Scott is a passionate advocate for people and talent development. Scott graduated with the Superintendent’s Award for Excellence (Star Wreath) from the United States Military Academy at West Point, NY. After serving as a Captain in the U.S. Army, Scott received his MBA from the University of Minnesota, Carlson School of Management – Minneapolis, MN.

“As we expect FDA approval by the end of 2024, the hiring of an experienced commercial leader is instrumental in further accelerating our U.S. go–to–market strategy into a concrete launch execution plan. This starts with having a commercial team fully operational by year–end. Scott is a dynamic and creative leader with countless accomplishments in building high–performing teams and developing new markets for innovative technologies,” commented Olivier Taelman, Nyxoah Chief Executive Officer. “This appointment is the kickoff of building a team of world–class patient– and clinician–focused professionals, supporting Nyxoah’s mission to make sleep simple again for OSA patients.”

“This is a promising time for patients with OSA. Nyxoah’s strong DREAM study results and Genio’s success in markets outside of the U.S. have demonstrated the potential of Genio’s breakthrough and unique solution. Both patients and physicians are eagerly awaiting a second player in the HGNS field. I am thrilled to be part of the team building out a patient–focused commercial operation that prioritizes the success of our healthcare provider partners in treating OSA,” added Scott.

About Nyxoah
Nyxoah 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 announced positive outcomes from the DREAM IDE pivotal study for FDA and U.S. commercialization approval.

For more information, please see the Company’s annual report for the financial year 2023 and 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 entry into of the loan facility agreement and the synthetic warrant agreement with the EIB; the use of proceeds from the loan facility agreement; the Genio® system 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; reporting data from Nyxoah’s DREAM U.S. pivotal trial; filing for FDA approval; and entrance to the U.S. market. 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.

Contact:

Nyxoah
David DeMartino, Chief Strategy Officer
IR@nyxoah.com

For Media
Belgium/France
Backstage Communication – Gunther De Backer
gunther@backstagecom.be

International/Germany
MC Services – Anne Hennecke
anne.hennecke@mc–services.eu

Attachment


GLOBENEWSWIRE (Distribution ID 1000971439)

Nyxoah Has Signed a €37.5 Million Loan Facility Agreement with the European Investment Bank

REGULATED INFORMATION
INSIDE INFORMATION

Nyxoah Has Signed a €37.5 Million Loan Facility Agreement with the European Investment Bank

Mont–Saint–Guibert, Belgium – July 3, 2024, 12:30pm CET / 6:30am 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 announced that it has signed a €37.5 million loan facility agreement with the European Investment Bank (“EIB”). The agreement is backed by the European Commission’s InvestEU program. Nyxoah plans to use the funding for research and development, and for scaling–up its manufacturing capacity to meet demand in Europe and the U.S.

The €37.5 million facility is divided into three tranches: €10 million for the first tranche (“Tranche A”), €13.75 million for the second tranche (“Tranche B”) and €13.75 million for the third tranche (“Tranche C”). Disbursement under the various tranches is subject to certain conditions. Tranche A carries an annual 5% cash and 5% capitalized interest rate, and features a five–year bullet repayment schedule. The various tranches do not contain revenue or liquidity covenants.

In connection with the loan facility agreement, and as a condition to drawdown thereunder, the Company also intends to enter into a “synthetic warrant agreement” with the EIB. Under the intended synthetic warrant agreement, in consideration for the facility, in connection with each tranche of the facility, the EIB will be granted “synthetic warrants” with a duration of 20 years. The number and strike price of the synthetic warrants will be calculated based on tranche specific formulas provided for in the synthetic warrant agreement. The synthetic warrants can be exercised as of the maturity date of the relevant tranche of the facility or, in exceptional situations, earlier. Such synthetic warrants will entitle the EIB to receive from the Company a cash consideration equal to the 20–day volume weighted average price of a share in the Company on the stock exchange, reduced by the applicable strike price per synthetic warrant, and multiplied by the number of synthetic warrants that the EIB exercises. In connection with Tranche A, it is expected that the EIB will be granted 468,384 synthetic warrants with a strike price of €8,11 that the EIB can exercise after the maturity of Tranche A (5 years) or, in exceptional situations, earlier.

Since certain provisions of the loan facility agreement and the synthetic warrant agreement are dependent on a change of control, those provisions will be submitted for approval to a shareholders' meeting of the Company in accordance with article 7:151 of the Belgian Companies and Associations Code.

EIB Vice–President Robert de Groot said: “Belgium stands at the forefront of innovation in the area of life sciences and med tech. As the EIB, we take pride in supporting this thriving industry and fostering growth. Nyxoah, with its groundbreaking approach, is making a valuable contribution. We are eager to see the company progressing, benefitting patients worldwide.”

Olivier Taelman, CEO of Nyxoah, commented: “We are excited and grateful for the support and confidence in our cutting–edge technology shown by the European Investment Bank. This loan follows our recent successful equity offering where we raised €48.5 million, providing us a combined access to over €80 million in growth capital. This will aid in the commercialization of Genio in Europe and in the U.S., if approved, while helping increase production capacity and sustain innovation.”

About Nyxoah
Nyxoah 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 announced positive outcomes from the DREAM IDE pivotal study for FDA and U.S. commercialization approval.

For more information, please see the Company’s annual report for the financial year 2023 and 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 entry into of the loan facility agreement and the synthetic warrant agreement with the EIB; the use of proceeds from the loan facility agreement; the Genio® system 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; reporting data from Nyxoah’s DREAM U.S. pivotal trial; filing for FDA approval; and entrance to the U.S. market. 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:

Nyxoah
David DeMartino, Chief Strategy Officer
IR@nyxoah.com

For Media
Belgium/France
Backstage Communication – Gunther De Backer
gunther@backstagecom.be

International/Germany
MC Services – Anne Hennecke
anne.hennecke@mc–services.eu

Attachment


GLOBENEWSWIRE (Distribution ID 1000969769)

Nyxoah a Signé une Convention de Prêt de 37,5 Millions d'Euros avec la Banque Européenne d'Investissement

Nyxoah a Signé une Convention de Prêt de 37,5 Millions d'Euros avec la Banque Européenne d'Investissement

INFORMATIONS PRIVILÉGIÉES
INFORMATIONS RÉGLEMENTÉES

Nyxoah a Signé une Convention de Prêt de 37,5 millions d'euros avec la Banque Européenne d'Investissement

Mont–Saint–Guibert, Belgique – 3 juillet 2024, 12h30 CET / 6h30 ET – Nyxoah SA (Euronext Brussels/ Nasdaq : NYXH) (“Nyxoah” ou la “Société”) opère dans le secteur des technologies médicales et se concentre sur le développement et la commercialisation de solutions innovantes destinées à traiter le Syndrome d’Apnées Obstructives du Sommeil (SAOS). La Société a annoncé aujourd’hui la signature d’une convention de prêt de 37,5 millions d'euros avec la Banque Européenne d'Investissement (” BEI “). Cet accord est soutenu par le programme InvestEU de la Commission européenne. Nyxoah prévoit d’utiliser ce financement pour la recherche et le développement, ainsi que pour augmenter sa capacité de production afin de répondre à la demande en Europe et aux États–Unis.

La convention de prêt de 37,5 millions d'euros est divisée en trois tranches : 10 millions d'euros pour la première tranche (“Tranche A”), 13,75 millions d'euros pour la deuxième tranche (“Tranche B”) et 13,75 millions d'euros pour la troisième tranche (“Tranche C”). Le déboursement des différentes tranches est soumis à certaines conditions. La tranche A est assortie d'un taux d'intérêt annuel de 5 % au comptant et de 5 % capitalisé. Le remboursement du capital se fera à l’échéance de la tranche après 5 ans. Les différentes tranches ne contiennent pas d'engagements en matière de revenus ou de liquidités.

Dans le cadre de l'accord relatif à la convention de prêt, et comme condition à son utilisation, la Société a également l'intention de conclure un “accord de warrants synthétiques” avec la BEI. En vertu de cet accord, la BEI recevra, en contrepartie de la facilité de crédit, des ” warrants synthétiques ” d'une durée de 20 ans pour chaque tranche de la facilité de crédit. Le nombre et le prix d'exercice des warrants synthétiques seront calculés sur la base de formules spécifiques à chaque tranche prévues dans l'accord sur les warrants synthétiques. Les warrants synthétiques peuvent être exercés à partir de la date d'échéance de la tranche concernée de la facilité ou, dans des situations exceptionnelles, plus tôt. Ces warrants synthétiques permettront à la BEI de recevoir de la Société une contrepartie en espèces égale au prix moyen pondéré en fonction du volume sur 20 jours d'une action de la Société en bourse, diminué du prix d'exercice applicable par warrant synthétique, et multiplié par le nombre de warrants synthétiques que la BEI exerce. Dans le cadre de la tranche A, il est prévu que la BEI reçoive 468 384 warrants synthétiques avec un prix d'exercice de 8,11 € que la BEI pourra exercer après l'échéance de la tranche A (5 ans) ou, dans des situations exceptionnelles, plus tôt.

Étant donné que certaines dispositions de la convention de prêt et de la convention de warrants synthétiques dépendent d'un changement de contrôle, ces dispositions seront soumises à l'approbation d'une assemblée générale des actionnaires de la Société conformément à l'article 7:151 du Code belge des Sociétés et des Associations.
Robert de Groot, Vice–Président de la BEI, a déclaré : ” La Belgique est à la pointe de l'innovation dans le domaine des sciences de la vie et des technologies médicales. En tant que BEI, nous sommes fiers de soutenir cette industrie florissante et de favoriser la croissance. Nyxoah, avec son approche novatrice, apporte une contribution précieuse. Nous sommes impatients de voir la société progresser, au bénéfice des patients du monde entier.”

Olivier Taelman, CEO de Nyxoah, a commenté l'événement : “Nous sommes ravis et reconnaissants du soutien et de la confiance que la Banque européenne d'investissement accorde à notre technologie de pointe. Ce prêt fait suite au succès de notre récente émission d'actions, qui nous a permis de lever 48,5 millions d'euros, ce qui nous donne un accès combiné à plus de 80 millions d'euros de capital. Cela nous aidera à commercialiser le Genio en Europe et aux États–Unis, s'il est approuvé, tout en contribuant à augmenter la capacité de production et à soutenir l'innovation.

A propos de Nyxoah

Nyxoah opère dans le secteur des technologies médicales. Elle se concentre sur le développement et la commercialisation de solutions innovantes destinées à traiter le Syndrome d’Apnées Obstructives du Sommeil (SAOS). La principale solution de Nyxoah est le système Genio®, une thérapie de neurostimulation du nerf hypoglosse sans sonde et sans batterie qui a reçu le marquage CE, centrée sur le patient et destinée à traiter le Syndrome d’Apnées Obstructives du Sommeil (SAOS), le trouble respiratoire du sommeil le plus courant au monde. Ce dernier est associé à un risque accru de mortalité et des comorbidités, dont les maladies cardiovasculaires. La vision de Nyxoah est que les patients souffrant de SAOS doivent pouvoir profiter de nuits réparatrices et vivre pleinement leur vie.

À la suite de la réussite de l'étude BLAST OSA, le système Genio® a reçu son marquage CE européen en 2019. Nyxoah a réalisé deux introductions en bourse réussies : sur Euronext Bruxelles en septembre 2020 et sur le NASDAQ en juillet 2021. Suite aux résultats positifs de l'étude BETTER SLEEP, Nyxoah a reçu l'approbation du marquage CE pour l'élargissement de ses indications thérapeutiques aux patients atteints de Collapse Concentrique Complet (CCC), actuellement contre–indiqués dans la thérapie des concurrents. En outre, la Société mène actuellement l'étude pivot DREAM IDE en vue d'obtenir l'approbation FDA et de commercialisation aux États–Unis.

Pour plus d'informations, veuillez consulter le rapport annuel de la société pour l'exercice 2023 et visiter le site suivant http://www.nyxoah.com/.

Attention – Marquage CE depuis 2019. Dispositif expérimental aux États–Unis. Limité par la loi fédérale américaine à un usage expérimental aux États–Unis.

Déclarations Prospectives

Certaines déclarations, croyances et opinions contenues dans le présent communiqué de presse sont de nature prospective et reflètent les attentes actuelles de la société ou, le cas échéant, des administrateurs ou de la direction de la société concernant la conclusion de l'accord de facilité de prêt et de l'accord de bons de souscription synthétiques avec la BEI, l'utilisation du produit de l'accord de facilité de prêt ; le système Genio® et les études cliniques en cours sur le système Genio® ; les avantages potentiels du système Genio® ; les objectifs de Nyxoah concernant le développement, la voie réglementaire et l'utilisation potentielle du système Genio® ; l'utilité des données cliniques pour l'obtention éventuelle de l'approbation de la FDA pour le système Genio® ; la communication des données de l'essai pivot DREAM U. U. de Nyxoah, le dépôt d'une demande d'approbation auprès de la FDA et l'entrée sur le marché américain. De par leur nature, les déclarations prospectives impliquent un certain nombre de risques, d'incertitudes, d'hypothèses et d'autres facteurs susceptibles d'entraîner une différence matérielle entre les résultats ou événements réels et ceux exprimés ou sous–entendus dans les déclarations prospectives. Ces risques, incertitudes, hypothèses et facteurs pourraient avoir une incidence négative sur les résultats et les effets financiers des plans et des événements décrits dans le présent document. En outre, ces risques et incertitudes comprennent, sans s'y limiter, les risques et incertitudes énoncés dans la section “Facteurs de risque” du rapport annuel de la société sur le formulaire 20–F pour l'exercice clos le 31 décembre 2023, déposé auprès de la Securities and Exchange Commission (“SEC”) le 20 mars 2024, et des rapports ultérieurs que la société dépose auprès de la SEC. Une multitude de facteurs, y compris, mais sans s'y limiter, les changements dans la demande, la concurrence et la technologie, peuvent faire en sorte que les événements, les performances ou les résultats réels diffèrent de manière significative de tout développement anticipé. Les déclarations prospectives contenues dans le présent communiqué de presse concernant des tendances ou des activités passées ne constituent pas des garanties de performances futures et ne doivent pas être considérées comme une déclaration selon laquelle ces tendances ou activités se poursuivront à l'avenir. En outre, même si les résultats ou développements réels sont conformes aux déclarations prospectives contenues dans le présent communiqué de presse, ces résultats ou développements peuvent ne pas être représentatifs des résultats ou développements des périodes futures. Aucune déclaration ou garantie n'est donnée quant à l'exactitude ou à la justesse de ces déclarations prévisionnelles. En conséquence, la Société décline expressément toute obligation ou tout engagement de publier des mises à jour ou des révisions des déclarations prospectives contenues dans le présent communiqué de presse à la suite d'un changement des attentes ou d'un changement des événements, conditions, hypothèses ou circonstances sur lesquels ces déclarations prospectives sont basées, sauf si la loi ou la réglementation l'exige expressément. Ni la Société, ni ses conseillers ou représentants, ni aucune de ses filiales, ni les dirigeants ou employés de ces personnes ne garantissent que les hypothèses sous–jacentes à ces déclarations prospectives sont exemptes d'erreurs et n'acceptent aucune responsabilité quant à l'exactitude future des déclarations prospectives contenues dans ce communiqué de presse ou quant à la survenance effective des développements prévus. Vous ne devriez pas accorder une confiance excessive aux déclarations prospectives, qui ne sont valables qu'à la date du présent communiqué de presse.

Contact :

Nyxoah
David DeMartino, Chief Strategy Officer
IR@nyxoah.com

Media
Belgique / France
Backstage Communication – Gunther De Backer
gunther@backstagecom.be

International/ Allemagne
MC Services – Anne Hennecke
anne.hennecke@mc–services.eu

 

GLOBENEWSWIRE (Distribution ID 1000969769)

DigiAsia Corp. Announces Completion of Convertible Note Financing with Helena Partners and Extinguishes Outstanding Debt

~ Prompt Extinguishment of Debt Following Recent Listing as a Public Company Prioritizes Financial Responsibility with a Healthy Capital Structure ~

NEW YORK, July 02, 2024 (GLOBE NEWSWIRE) — DigiAsia Corp. (NASDAQ: FAAS) (“DigiAsia” or the “Company”), a leading Fintech as a Service (“FaaS”) ecosystem provider, today announced it has received net proceeds of $3.0 million as a result of the previously announced Securities Purchase Agreement (“SPA”) with Helena Special Opportunities LLC, an affiliate of Helena Partners Inc. (“Helena”). In addition, through the issuance of Senior Unsecured Convertible Notes (the “Notes”), convertible into Class A common shares of the Company, and $5.2 million of Class B Convertible Notes, DigiAsia has extinguished all debt inherited from its business combination with StoneBridge Acquisition Corporation. The remainder of proceeds will be utilized for general corporate purposes as growth capital investment.

As announced on June 21, 2024, the Notes bear interest at a rate of 12% per annum, payable quarterly, and mature one year from the issuance of the note. Helena, pursuant to its note, has the option, on or prior to the maturity date, to convert the entire principal amount and all accrued but unpaid interest on the notes into shares of DigiAsia common stock.

EF Hutton LLC acted as the exclusive placement agent for the offering. Winston & Strawn LLP acted as legal advisor to DigiAsia.

Forward–Looking Statements:

This press release may contain forward–looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. The words “believe”, “expect”, “anticipate”, “project”, “targets”, “optimistic”, “confident that”, “continue to”, “predict”, “intend”, “aim”, “will” or similar expressions are intended to identify forward–looking statements. All statements other than statements of historical fact are statements that may be deemed forward–looking statements. These forward–looking statements including, but not limited to, statements concerning DigiAsia and the Company’s operations, financial performance and condition are based on current expectations, beliefs and assumptions which are subject to change at any time. DigiAsia cautions that these statements by their nature involve risks and uncertainties, and actual results may differ materially depending on a variety of important factors such as government and stock exchange regulations, competition, political, economic and social conditions around the world including those discussed in DigiAsia’s Form 20–F under the headings “Risk Factors”, “Management’s Discussion and Analysis of Financial Condition and Results of Operations” and “Business Overview” and other reports filed with the Securities and Exchange Commission from time to time. All forward–looking statements are applicable only as of the date it is made and DigiAsia specifically disclaims any obligation to maintain or update the forward–looking information, whether of the nature contained in this release or otherwise, in the future.

DigiAsia Company Contact:

Subir Lohani

Chief Financial Officer and Chief Strategy Officer

646–480–0142

Investor Contact:

MZ North America

Email: FAAS@mzgroup.us


GLOBENEWSWIRE (Distribution ID 9172144)

Nyxoah Submits Fourth and Final Module in PMA Application for Genio to the US FDA

Nyxoah Submits Fourth and Final Module in PMA Application for Genio to the US FDA

Mont–Saint–Guibert (Belgium), July 1, 2024, 8:00am CET / 2:00am ET – (“Nyxoah” or the “Company”), a medical technology company focused on the development and commercialization of innovative solutions to treat Obstructive Sleep Apnea (OSA), today announced that the Company submitted the fourth and final module of its Premarket Approval (PMA) application for Genio to the U.S. Food and Drug Administration (FDA).

Genio is a different approach to hypoglossal nerve stimulation (HGNS). Genio offers patients a leadless, fully–body MRI compatible, non–implanted battery solution, powered and controlled by a wearable. Thanks to the fully upgradable wearable component, Genio patients can always have access to the most advanced technology without needing another surgery. In March 2024, Nyxoah announced the DREAM U.S. pivotal study data achieved a statistically significant reduction in the co–primary endpoints of 12–month AHI responder rate, per the Sher criteria, and ODI responder rate, both on an intent–to–treat basis, and that Genio is the only HGNS solution to show similar outcomes in supine and non–supine sleep.

“I am proud to achieve this important milestone, which brings us one step closer to offering Genio to obstructive sleep apnea patients in the U.S. I would like to congratulate our entire team on their hard work in completing the PMA submission. I could not be more excited for the remainder of 2024, which includes presenting the complete DREAM data at the International Surgical Sleep Society meeting in September and preparing for a U.S. launch by the end of the year,” commented Olivier Taelman, Nyxoah’s Chief Executive Officer.

About Nyxoah
Nyxoah 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.

Contact:

Nyxoah
David DeMartino, Chief Strategy Officer
IR@nyxoah.com

For Media
Belgium/France
Backstage Communication – Gunther De Backer
gunther@backstagecom.be

International/Germany
MC Services – Anne Hennecke
anne.hennecke@mc–services.eu

Attachment


GLOBENEWSWIRE (Distribution ID 1000969145)