Alterity Therapeutics Raises A$40.0 million in Placement
Rhea-AI Summary
Alterity Therapeutics (NASDAQ: ATHE) has secured binding commitments for a A$40.0 million capital raise through a two-tranche placement of ordinary shares to institutional and sophisticated investors. The placement was conducted at A$0.011 per share, an 8.3% discount to the last closing price, with one free attaching option for every three new shares issued.
The funding will primarily support the advancement of ATH434, their lead compound for neurodegenerative diseases, which recently showed significant results in Multiple System Atrophy (MSA) treatment. The Phase 2 clinical trial demonstrated a 48% slowing of clinical progression at the 50mg dose and favorable safety profile.
The placement consists of a A$12.8 million Tranche One (1.2 billion shares) and a A$27.2 million Tranche Two (2.5 billion shares), with the latter requiring shareholder approval at an Extraordinary General Meeting expected in March 2025.
Positive
- Secured A$40.0 million in new capital funding
- Phase 2 trial showed 48% slowing of clinical progression in MSA
- ATH434 demonstrated favorable safety profile in clinical trials
- Strong support from institutional investors
Negative
- 8.3% share price discount for the placement
- Significant dilution with 3.7 billion new shares being issued
- Tranche Two requires shareholder approval, creating execution risk
Insights
The A$40 million capital raise ($26.4M USD) marks a pivotal moment for Alterity Therapeutics, providing important funding for their promising MSA treatment pipeline. The placement's structure reveals sophisticated financial engineering:
The two-tranche approach, with A$12.8M in Tranche One and A$27.2M in Tranche Two, balances immediate capital needs with shareholder approval requirements. The inclusion of one free attaching option for every three shares, with a A$0.028 exercise price, provides potential additional future funding while offering investors upside participation.
The timing of this raise is particularly strategic, following the recent positive Phase 2 results showing a remarkable 48% slowing of clinical progression in MSA patients. This data-driven approach has attracted institutional investors, suggesting strong market confidence in ATH434's potential.
From a financial perspective, this raise significantly extends the company's operational runway. Based on typical Phase 2 to Phase 3 development costs in neurodegenerative diseases, this funding could support accelerated regulatory discussions with the FDA and initial Phase 3 preparation work. The focus on MSA, a rare disease with treatment options, could potentially qualify for expedited regulatory pathways, optimizing capital efficiency.
The dilution impact, while substantial with 3.7 billion new shares, is offset by the company's strengthened negotiating position for future partnerships or financing rounds. The strong institutional backing, particularly from international investors, provides validation of ATH434's market potential in the $5 billion Parkinsonian disorders market.
– Funds to be used primarily to advance development of ATH434 in Parkinsonian Disorders –
– Capital raising was strongly supported by domestic and international institutional investors –
MELBOURNE, Australia and SAN FRANCISCO, Feb. 10, 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 grateful for the strong response from the investment community and are proud to welcome a number of leading domestic and international institutions as shareholders in support of Alterity as we advance our lead compound ATH434 for the treatment of neurodegenerative diseases,” said David Stamler, M.D., Chief Executive Officer of Alterity. “ATH434 has demonstrated significant slowing of clinical progression and a favourable safety profile in Multiple System Atrophy (MSA), a rare and rapidly progressive disease. We will use funds from this capital raise to accelerate ATH434 regulatory and development activities and to continue research and discovery of novel compounds for major indications such as Parkinson’s disease. Given the strength of the data and the tremendous unmet need for treating MSA, I am looking forward to engaging with FDA on the best path to bring ATH434 to individuals with MSA as soon as possible.”
MST Financial Services Pty Ltd (MST) acted as sole manager of the offering.
Placement details
The Placement was fully subscribed and was conducted at A
Tranche one of the Placement is to raise approximately A
Tranche two of the Placement is expected to raise approximately A
Tranche Two of the Placement includes an aggregate of A
The new shares to be issued will rank equally with existing ATH fully paid ordinary shares.
Further details are set out in the Appendix 3B released to ASX at or about the same time as this announcement.
Use of Proceeds
The use of proceeds from this financing will provide Alterity a strong balance sheet to fund ongoing clinical development programs for ATH434, including planned advancements in MSA, continuing discovery and research efforts in neurodegenerative diseases, including Parkinson’s Disease, and general working capital.
At the end of January, the company released positive topline results from its ATH434-201 Phase 2 clinical trial of ATH434. The data demonstrated a clinically meaningful benefit at both ATH434 doses studied and the trial achieved statistical significance at the 50 mg dose with
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’s lead asset, ATH434, has the potential to treat various Parkinsonian disorders and is currently being evaluated in two Phase 2 clinical trials in Multiple System Atrophy. Alterity also 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 Company’s web site at www.alteritytherapeutics.com.
Authorisation & Additional information
This announcement was authorized by David Stamler, CEO of Alterity Therapeutics Limited.
Investor and Media Contacts:
Australia
Ana Luiza Harrop
we-aualteritytherapeutics@we-worldwide.com
+61 452 510 255
U.S.
Remy Bernarda
remy.bernarda@iradvisory.com
+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 “Risk Factors” in the Company’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 Company’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 Company’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.