Alterity Therapeutics Raises A$20.0 million in Strategic Placement
Alterity Therapeutics (NASDAQ: ATHE) has secured binding commitments for a A$20.0 million capital raise through a placement of fully paid ordinary shares to international and Australian professional investors. The placement was conducted at A$0.012 per share, representing a 7.7% discount to the last ASX closing price.
The funding follows positive Phase 2 clinical trial results for ATH434 in Multiple System Atrophy (MSA), which demonstrated clinically meaningful benefits and a favorable safety profile. The proceeds will support non-clinical studies, CMC activities, clinical and regulatory activities for ATH434's development in MSA, and general working capital. The company plans to engage with the FDA to discuss the path forward for ATH434's development.
Alterity Therapeutics (NASDAQ: ATHE) ha ottenuto impegni vincolanti per un aumento di capitale di A$20,0 milioni mediante un collocamento di azioni ordinarie totalmente liberate a investitori professionali internazionali e australiani. Il collocamento è stato effettuato a A$0,012 per azione, pari a uno sconto del 7,7% rispetto all'ultimo prezzo di chiusura ASX.
Il finanziamento segue i risultati positivi dello studio clinico di Fase 2 su ATH434 nella Atrofia Multisistemica (MSA), che hanno evidenziato benefici clinicamente significativi e un profilo di sicurezza favorevole. I proventi sosterranno studi non clinici, attività CMC, attività cliniche e regolatorie per lo sviluppo di ATH434 nella MSA e il capitale circolante generale. L'azienda intende confrontarsi con la FDA per definire il percorso di sviluppo futuro di ATH434.
Alterity Therapeutics (NASDAQ: ATHE) ha asegurado compromisos vinculantes para una captación de capital de A$20,0 millones mediante una colocación de acciones ordinarias totalmente desembolsadas a inversores profesionales internacionales y australianos. La colocación se realizó a A$0,012 por acción, lo que representa un descuento del 7,7% respecto al último cierre en la ASX.
La financiación sigue a los resultados positivos del ensayo clínico de Fase 2 de ATH434 en Atrofia Multisistémica (MSA), que mostraron beneficios clínicamente relevantes y un perfil de seguridad favorable. Los fondos se destinarán a estudios no clínicos, actividades CMC, actividades clínicas y regulatorias para el desarrollo de ATH434 en MSA y a capital de trabajo general. La compañía planea reunirse con la FDA para definir el siguiente paso en el desarrollo de ATH434.
Alterity Therapeutics (NASDAQ: ATHE)� 국제 � 호주 전문 투자자들� 대상으� 보통� 전액 납입 방식� 배정� 통해 A$20.0백만 규모� 자금 조달� 대� 구속� 있는 약속� 확보했습니다. 이번 배정은 주당 A$0.012� 이루어졌으며, 이는 직전 ASX 종가 대� 7.7% 할인� 해당합니�.
이번 자금조달은 ATH434� 다계� 위축�(MSA) 대� 2� 임상시험에서 임상적으� 의미 있는 효과와 우호적인 안전� 프로파일� 확인� 긍정� 결과� 따른 것입니다. 수익금은 비임� 연구, CMC 활동, ATH434� MSA 개발� 위한 임상 � 규제 활동, 일반 운전자본� 지원하� � 사용� 예정입니�. 회사� ATH434 개발� 향후 경로� 논의하기 위해 FDA와 협의� 계획입니�.
Alterity Therapeutics (NASDAQ: ATHE) a obtenu des engagements contraignants pour une levée de fonds de A$20,0 millions via un placement d'actions ordinaires libérées auprès d'investisseurs professionnels internationaux et australiens. Le placement a été réalisé à A$0,012 par action, soit une décote de 7,7 % par rapport au dernier cours de clôture à l'ASX.
Ce financement fait suite aux résultats positifs de l'essai clinique de phase 2 d'ATH434 dans l'atrophie multisystémique (MSA), qui ont montré des bénéfices cliniquement significatifs et un profil de sécurité favorable. Les produits serviront à financer des études non cliniques, des activités CMC, des activités cliniques et réglementaires pour le développement d'ATH434 dans la MSA, ainsi que le fonds de roulement général. La société prévoit de s'entretenir avec la FDA pour discuter de la suite du développement d'ATH434.
Alterity Therapeutics (NASDAQ: ATHE) hat verbindliche Zusagen für eine Kapitalerhöhung in Höhe von A$20,0 Millionen durch eine Platzierung von voll eingezahlten Stammaktien bei internationalen und australischen Profi-Investoren erhalten. Die Platzierung erfolgte zu A$0,012 pro Aktie, was einem Abschlag von 7,7% gegenüber dem letzten ASX-Schlusskurs entspricht.
Die Mittelzufuhr erfolgt nach positiven Ergebnissen der Phase-2-Studie mit ATH434 bei der Multisystematrophie (MSA), die klinisch relevante Vorteile und ein günstiges Sicherheitsprofil zeigte. Die Erlöse werden nichtklinische Studien, CMC-Aktivitäten, klinische und regulatorische Maßnahmen für die Entwicklung von ATH434 bei MSA sowie das allgemeine Working Capital unterstützen. Das Unternehmen plant, mit der FDA über den weiteren Entwicklungsweg von ATH434 zu sprechen.
- Successful raise of A$20.0 million with modest 7.7% discount and no options
- Positive Phase 2 clinical trial results showing clinically meaningful benefit for ATH434
- Strategic investment from high-quality international healthcare-focused fund
- Strengthened institutional register and balance sheet for pursuing partnerships
- 7.7% share price dilution for existing shareholders
Insights
Alterity secures A$20M funding following positive Phase 2 MSA trial results, strengthening its position for regulatory discussions and partnerships.
Alterity Therapeutics has secured
The financing was anchored by a high-quality international healthcare-focused fund, which speaks to the growing institutional confidence in Alterity's clinical program. Notably, this capital raise was executed without warrants or options, avoiding potential future dilution that often accompanies biotech fundraising at this stage.
The timing is strategically significant as it follows the company's announcement of "robust efficacy" demonstrated in their Phase 2 MSA trials. The funds will specifically support non-clinical studies, chemical manufacturing and controls (CMC) activities, and regulatory engagement - all critical components for advancing ATH434 toward potential approval.
Perhaps most importantly, management has indicated they will use this strengthened balance sheet position to pursue strategic partnerships, suggesting they're preparing for potential licensing deals or other collaborative arrangements that could further accelerate development. The planned FDA engagement to discuss the regulatory pathway forward represents a critical near-term catalyst that could significantly impact the company's timeline to potential commercialization.
MELBOURNE, Australia and SAN FRANCISCO, Sept. 08, 2025 (GLOBE NEWSWIRE) -- Alterity Therapeutics (ASX: ATH, NASDAQ: ATHE) (“Alterity� or “the Company�), a biotechnology company dedicated to developing disease modifying treatments for neurodegenerative diseases, today announced it has received binding commitments for a capital raising of A
"We are thankful for the continued interest from the investment community following the robust efficacy we demonstrated in our Phase 2 clinical trial in Multiple System Atrophy. We look forward to an exciting twelve months ahead as we actively pursue the path to approval,� said, David Stamler, M.D., Chief Executive Officer of Alterity. “We elected to execute this placement due to inbound interest from a high-quality international healthcare-focused fund that anchored the transaction. Based on the promising outlook for the company, we raised these funds at a modest discount with no options. The additional funding allows us to continue advancing our clinical and regulatory strategy for ATH434 with the US FDA and other agencies, while at the same time it strengthens our institutional register and balance sheet to best position the company for pursuing strategic partnerships.�
MST Financial Services Pty Ltd (MST) acted as sole manager of the offering.
Placement details
The Placement was conducted at A
Use of Proceeds
The use of proceeds from this financing will provide Alterity a strong balance sheet to fund the necessary non-clinical studies, chemical manufacturing and controls (CMC) activities, clinical and regulatory activities for future development of ATH434 in MSA, and general working capital.
During 2025, Alterity has released positive topline results from its ATH434-201 and ATH434-202 Phase 2 clinical trials of ATH434. The data have demonstrated a clinically meaningful benefit and a favorable safety profile. Based on the strength of these Phase 2 data, the company plans to engage with the FDA to discuss the path forward for future development of ATH434.
About Alterity Therapeutics Limited
Alterity Therapeutics is a clinical stage biotechnology company dedicated to creating an alternate future for people living with neurodegenerative diseases. The Company is initially focused on developing disease modifying therapies in Parkinson’s disease and related disorders. Alterity has demonstrated clinically meaningful efficacy for its lead asset, ATH434, in a randomized, double-blind, placebo-controlled Phase 2 clinical trial in participants with Multiple System Atrophy (MSA), a rare and rapidly progressive Parkinsonian disorder. ATH434 recently reported positive data in its open label Phase 2 clinical trial in advanced MSA. In addition, Alterity has a broad drug discovery platform generating patentable chemical compounds to treat the underlying pathology of neurological diseases. The Company is based in Melbourne, Australia, and San Francisco, California, USA. For further information please visit the dz貹Բ’s website at .
Authorisation & Additional information
This announcement was authorized by David Stamler, CEO of Alterity Therapeutics Limited.
Investor and Media Contacts:
Australia
Ana Luiza Harrop
+61 452 510 255
U.S.
Remy Bernarda
+1 (415) 203-6386
Forward Looking Statements
This press release contains "forward-looking statements" within the meaning of section 27A of the Securities Act of 1933 and section 21E of the Securities Exchange Act of 1934. The Company has tried to identify such forward-looking statements by use of such words as "expects," "intends," "hopes," "anticipates," "believes," "could," "may," "evidences" and "estimates," and other similar expressions, but these words are not the exclusive means of identifying such statements.
Important factors that could cause actual results to differ materially from those indicated by such forward-looking statements are described in the sections titled 辱 ٴǰ� in the dz貹Բ’s filings with the SEC, including its most recent Annual Report on Form 20-F as well as reports on Form 6-K, including, but not limited to the following: statements relating to the Company's drug development program, including, but not limited to the initiation, progress and outcomes of clinical trials of the Company's drug development program, including, but not limited to, ATH434, and any other statements that are not historical facts. Such statements involve risks and uncertainties, including, but not limited to, those risks and uncertainties relating to the difficulties or delays in financing, development, testing, regulatory approval, production and marketing of the dz貹Բ’s drug components, including, but not limited to, ATH434, the ability of the Company to procure additional future sources of financing, unexpected adverse side effects or inadequate therapeutic efficacy of the Company's drug compounds, including, but not limited to, ATH434, that could slow or prevent products coming to market, the uncertainty of obtaining patent protection for the Company's intellectual property or trade secrets, the uncertainty of successfully enforcing the dz貹Բ’s patent rights and the uncertainty of the Company freedom to operate.
Any forward-looking statement made by us in this press release is based only on information currently available to us and speaks only as of the date on which it is made. We undertake no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.
