NurExone Secures over C$3.18 Million Through Accelerated Warrant Exercises
NurExone (OTCQB: NRXBF) announced it received C$3,185,994.43 in gross proceeds from accelerated warrant exercises completed after acceleration notices issued on October 8, 2025.
The company reported C$1,207,418.88 from 2,515,456 September 2023 warrants at C$0.48 each and C$1,978,575.55 from 5,653,073 January 2024 warrants at C$0.35 each. Proceeds will be used for general corporate purposes and working capital to support development of its exosome-based therapeutic platform, including ExoPTEN. NurExone also received finalist recognition at Falling Walls (Berlin) and Prix Galien Bridges (Stockholm, December 5, 2025).
NurExone (OTCQB: NRXBF) ha annunciato di aver incassato 3.185.994,43 C$ di proventi lordi dall'esercizio accelerato di warrant completato dopo le notifiche di accelerazione emesse l'8 ottobre 2025.
L'azienda ha riportato 1.207.418,88 C$ da 2.515.456 warrant di settembre 2023 a 0,48 C$ ciascuno e 1.978.575,55 C$ da 5.653.073 warrant di gennaio 2024 a 0,35 C$ ciascuno. I proventi saranno utilizzati per scopi generali aziendali e capitale circolante per supportare lo sviluppo della sua piattaforma terapeutica basata su esosome, inclusa ExoPTEN. NurExone ha anche ricevuto riconoscimento tra i finalisti a Falling Walls (Berlino) e Prix Galien Bridges (Stockholm, 5 dicembre 2025).
NurExone (OTCQB: NRXBF) anunció que recibió C$3,185,994.43 en ingresos brutos por ejercicios acelerados de warrants realizados tras las notificaciones de aceleración emitidas el 8 de octubre de 2025.
La empresa reportó C$1,207,418.88 de 2,515,456 warrants de septiembre de 2023 a 0,48 C$ cada uno y C$1,978,575.55 de 5,653,073 warrants de enero de 2024 a 0,35 C$ cada uno. Los ingresos se utilizarán para fines corporativos generales y capital de trabajo para apoyar el desarrollo de su plataforma terapéutica basada en exosomas, incluida ExoPTEN. NurExone también recibió reconocimiento de finalista en Falling Walls (Berlín) y Prix Galien Bridges (Estocolmo, 5 de diciembre de 2025).
NurExone (OTCQB: NRXBF)은 2025년 10월 8일 발송된 가속화 고지 후 완료된 가속화 워런트 매수로 C$3,185,994.43의 총 수익금을 받았다고 발표했습니다.
또한 2023년 9월 만료 워런트 2,515,456주에서 0.48 C$씩, 2024년 1월 만료 워런트 5,653,073주에서 0.35 C$씩 각각 C$1,207,418.88과 C$1,978,575.55를 보고했습니다. 수익은 일반 기업 목적 및 운전자본으로 사용되어 ExoPTEN을 포함한 엑소좀 기반 치료 플랫폼 개발을 지원할 예정입니다. NurExone은 또한 Falling Walls(베를린)과 Prix Galien Bridges(스톡홀름, 2025년 12월 5일)에서 결선 진출상을 받았습니다.
NurExone (OTCQB: NRXBF) a annoncé avoir reçu 3 185 994,43 C$ de produits bruts provenant d'exercices accélérés de warrants réalisés après les avis d'accélération émis le 8 octobre 2025.
L'entreprise a déclaré 1 207 418,88 C$ provenant de 2 515 456 warrants de septembre 2023 à 0,48 C$ chacun et 1 978 575,55 C$ provenant de 5 653 073 warrants de janvier 2024 à 0,35 C$ chacun. Les produits seront utilisés pour des fins générales de l'entreprise et le fonds de roulement afin de soutenir le développement de sa plateforme thérapeutique à base d'exosomes, y compris ExoPTEN. NurExone a également reçu une reconnaissance de finaliste aux Falling Walls (Berlin) et Prix Galien Bridges (Stockholm, 5 décembre 2025).
NurExone (OTCQB: NRXBF) gab bekannt, dass es 3.185.994,43 C$ Bruttoerlöse aus beschleunigten Warrants-Erdaktionen nach Beschleunigungsbenachrichtigungen vom 8. Oktober 2025 erhalten hat.
Das Unternehmen meldete 1.207.418,88 C$ aus 2.515.456 September 2023 Warrants zu je 0,48 C$ und 1.978.575,55 C$ aus 5.653.073 Januar 2024 Warrants zu je 0,35 C$. Die Erlöse werden für allgemeine Geschäftszwecke und Working Capital verwendet, um die Entwicklung seiner exosom-basierten therapeutischen Plattform, einschließlich ExoPTEN, zu unterstützen. NurExone erhielt außerdem Finalisten-Erkennung bei Falling Walls (Berlin) und Prix Galien Bridges (Stockholm, 5. Dezember 2025).
NurExone (OTCQB: NRXBF) أعلنت أنها تلقّت 3,185,994.43 C$ من العائدات الإجمالية من تمارين الورنتس المتسارعة المكتملة بعد إشعارات التسريع الصادرة في 8 أكتوبر 2025.
وقد أفادت الشركة بأن 1,207,418.88 C$ من 2,515,456 ورنتس أيلول/سبتمبر 2023 عند 0.48 C$ لكل منها و 1,978,575.55 C$ من 5,653,073 ورنتس كانون الثاني/يناير 2024 عند 0.35 C$ لكل منها. ستُستخدم العوائد لأغراض عامة للشركة ورأس المال العامل لدعم تطوير منصتها العلاجية المستندة إلى الإكسوسومات، بما في ذلك ExoPTEN. كما تلقّت NurExone أيضاً اعترافاً كمرشحة نهائية في Falling Walls (برلين) و Prix Galien Bridges (ستوكهولم، 5 كانون الأول/ديسمبر 2025).
- Gross proceeds of C$3,185,994.43
- Exercise of 8,168,529 warrants completed
- Proceeds allocated to working capital and clinical development
- Full warrantholder participation signaling investor confidence
- Issuance of 8,168,529 shares from exercised warrants may dilute existing shareholders
NurExone Honored at Berlin and Stockholm Conferences for Breakthrough Contributions to Global Life Sciences and Health Innovation
TORONTO and HAIFA, Israel, Nov. 12, 2025 (GLOBE NEWSWIRE) -- NurExone Biologic Inc. (TSXV: NRX) (OTCQB: NRXBF) (FSE: J90) (“NurExone” or the “Company”) is pleased to announce that, further to its press release dated October 8, 2025 (the “October 8 Release”), the Company has received gross proceeds of over C
The breakdown of the proceeds is as follows: (i) C
Following the Company providing the outstanding holders of the September 2023 Warrants and January 2024 Warrants acceleration notices on October 8, 2025 notifying them that their acceleration triggers were met, when the daily volume average trading price of the Common Shares on the TSXV equaled or exceeded C
The proceeds from these exercises strengthen NurExone’s balance sheet and will be used for general corporate purposes and working capital, supporting ongoing development of Company’s exosome-based therapeutic platform.
Management Commentary
“We are very pleased with the full participation from warrantholders during the accelerated exercise period,” said Dr. Lior Shaltiel, Chief Executive Officer of NurExone. “This additional capital enhances our financial strengths as we continue advancing ExoPTEN and our therapeutic pipeline towards clinical readiness.”
Eran Ovadya, Chief Financial Officer of NurExone, added: “The full participation of these warrantholders reflects investor confidence in NurExone’s strategy and our exosome-based platform. The resulting funds provide further financial stability, enabling us to efficiently allocate resources towards clinical development and key operational priorities, while maintaining a strong balance sheet.”
Global Recognition of Translational Innovation
Alongside these financial milestones, NurExone’s scientific progress continues to gain international recognition. The Company has been nominated as a finalist for the Galien Foundation’s inaugural Prix Galien Bridges Awards. The award event, which will be held at the Nobel Forum in Stockholm on December 5, 2025, celebrates life sciences innovation that transcends geographic and disciplinary boundaries. Earlier this month, NurExone was also recognized as a finalist in the Falling Walls Science Breakthroughs of the Year Summit in Berlin.
“Our recognition among leading innovators in Europe, from Prix Galien in Stockholm to Falling Walls in Berlin, highlights our growing leadership position in exosome-based medicine,” noted Dr. Tali Kizhner, Director of Research and Development at NurExone. “We are proud to represent a new wave of regenerative biotechnology with the potential to connect scientific excellence with tangible human impact.”
About the Galien Foundation
The Galien Foundation fosters, recognizes, and rewards excellence in scientific innovation that improves the human condition. Established in honor of Galen, the father of modern medicine, the Galien Foundation oversees the international Prix Galien Bridges Awards, regarded as the industry’s highest accolade for biopharmaceutical research and innovation. The Prix Galien Bridges Awards extend this legacy by connecting innovators across regions and disciplines to advance the next generation of global health breakthroughs.
About NurExone
NurExone Biologic Inc. is a TSX Venture Exchange (“TSXV”), OTCQB, and Frankfurt-listed biotechnology company developing regenerative exosome-based therapies for central nervous system injuries. Its lead candidate, ExoPTEN, has shown compelling preclinical data supporting clinical potential in acute spinal cord and optic nerve injury, both multi-billion-dollar marketsi. Key regulatory milestones, including Orphan Drug Designation from the FDA and EMA, are paving the way towards clinical trials in the U.S. and Europe. NurExone has established Exo-Top Inc., a U.S. subsidiary, to produce and supply GMP-compliant exosomes for self-use, regenerative aesthetics and other indications as part of its commercial growth strategy.
For additional information and a brief interview, please watch Who is NurExone?, visit www.nurexone.com or follow NurExone on LinkedIn, Twitter, Facebook, or YouTube.
For more information, please contact:
Dr. Lior Shaltiel
Chief Executive Officer and Director
Phone: +972-52-4803034
Email: info@nurexone.com
Dr. Eva Reuter
Investor Relations – Germany
Phone: +49-69-1532-5857
Email: e.reuter@dr-reuter.eu
Allele Capital Partners
Investor Relations – U.S.
Phone: +1 978-857-5075
Email: aeriksen@allelecapital.com
FORWARD-LOOKING STATEMENTS
This press release contains certain “forward-looking statements” that reflect the Company’s current expectations and projections about its future results. Wherever possible, words such as “may”, “will”, “should”, “could”, “expect”, “plan”, “intend”, “anticipate”, “believe”, “estimate”, “predict” or “potential” or the negative or other variations of these words, or similar words or phrases, have been used to identify these forward-looking statements. Forward-looking statements in this press release include, but are not limited to, statements relating to: the use of proceeds and benefits from the warrant exercises; the benefits of being selected as a finalist and the opportunities that it may yield; the Company continuing to advance ExoPTEN and their therapeutic pipeline towards clinical readiness; and the NurExone platform technology offering novel solutions to drug companies interested in minimally invasive targeted drug delivery for other indications.
These statements reflect management’s current beliefs and are based on information currently available to management as at the date hereof. In developing the forward-looking statements in this press release, we have applied several material assumptions, including: ExoPTEN will yield the benefits outlined herein; being selected as a finalist will yield the benefits and opportunities outlined herein; the use of proceeds from the warrant exercises will be utilized as set out herein; the warrant exercises will have the benefits on the Company as set out herein; the Company will continue to advance ExoPTEN and their therapeutic pipeline towards clinical readiness; and the NurExone platform technology has the ability to offer novel solutions to drug companies interested in minimally invasive targeted drug delivery for other indications.
Forward-looking statements involve significant risk, uncertainties and assumptions. Many factors could cause actual results, performance or achievements to differ materially from the results discussed or implied in the forward-looking statements. These risks and uncertainties include, but are not limited to risks related to: the Company’s early stage of development; lack of revenues to date; the inherent uncertainty of preclinical drug development, including the risk that product candidates may not advance to clinical trials or receive regulatory approval; the possibility that results from preclinical studies and early-stage trials may not predict later outcomes; the uncertain timing, cost, and outcome of preclinical and clinical development activities; risks related to the clinical trial process, including potential delays or failure to achieve effective trial design or positive results; the inability to obtain or maintain required regulatory approvals; limited market acceptance of the Company’s products, even if approved; the potential emergence of competing therapies that are safer, more effective, or more affordable; rapid technological change that may impact the relevance of the Company’s technologies; the Company’s dependence on key personnel and strategic partners; the inability to obtain adequate financing; risks related to the Company’s ability to protect its intellectual property; the possibility that the Company’s technologies, including its exosome-based platforms, may not achieve their intended therapeutic impact; the inability to produce or scale exosome-based products for clinical use; limited adoption in regenerative medicine or cell therapy applications; lack of growing clinical demand in targeted indications such as spinal cord injury, optic nerve repair, or other therapeutic areas; failure to meet planned development milestones or achieve commercial breakthroughs; ExoPTEN will not yield the benefits outlined herein; being selected as a finalist will not yield the benefits and/or opportunities outlined herein; the use of proceeds from the warrant exercises will not be utilized as set out herein; the warrant exercises will not have the benefits on the Company as set out herein; the Company will be unable to continue to advance ExoPTEN and/or their therapeutic pipeline towards clinical readiness; the NurExone platform technology not offering novel solutions to drug companies interested in minimally invasive targeted drug delivery for other indications; and the risks discussed under the heading “Risk Factors” on pages 44 to 51 of the Company’s annual information form dated August 27, 2024, a copy of which is available under the Company’s SEDAR+ profile at www.sedarplus.ca . These factors should be considered carefully, and readers should not place undue reliance on the forward-looking statements. Although the forward-looking statements contained in this press release are based upon what management believes to be reasonable assumptions, the Company cannot assure readers that actual results will be consistent with these forward-looking statements. These forward-looking statements are made as of the date of this press release, and the Company assumes no obligation to update or revise them to reflect new events or circumstances, except as required by law.
Neither TSXV nor its Regulation Services Provider (as that term is defined in the policies of the TSXV) accepts responsibility for the adequacy or accuracy of this release.
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i Spinal cord injury, Glaucoma