Press Releases August 6, 2026 07:25 AM

Alterity Therapeutics to Present at the 46th Annual Canaccord Genuity Growth Conference

Alterity Therapeutics Announces CEO Presentation at 46th Annual Canaccord Genuity Growth Conference

By Marcus Reed
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ATHE

Alterity Therapeutics, a clinical-stage biotechnology company focused on neurodegenerative diseases, announced that CEO Dr. David Stamler will present at the Canaccord Genuity Growth Conference on August 11, 2026. The company is preparing for a Phase 3 pivotal trial of ATH434 for Multiple System Atrophy (MSA), having shown positive Phase 2 results. Alterity also highlighted its broad drug discovery platform aimed at neurological diseases.

Alterity Therapeutics to Present at the 46th Annual Canaccord Genuity Growth Conference
ATHE
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Key Points

  • Alterity is preparing to initiate a pivotal Phase 3 trial for ATH434 targeting Multiple System Atrophy (MSA), a rare neurodegenerative disease.
  • Positive Phase 2 clinical trial results demonstrate clinically meaningful efficacy of ATH434 in MSA patients.
  • The company maintains a broad drug discovery platform to develop treatments for neurological disorders.
  • The biotechnology and pharmaceutical sectors, especially those focused on neurodegenerative diseases, are directly impacted.

MELBOURNE, Australia and SAN FRANCISCO, Aug. 06, 2026 (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 that David Stamler, M.D., Chief Executive Officer, will present at the 46th Annual Canaccord Genuity Growth Conference on Tuesday, August 11, 2026 at 1:30 p.m. ET in the United States.

A link to the live and archived webcast may be accessed on Alterity Therapeutics website under the Investors section: Events and Presentations.

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 focused on developing disease modifying therapies in Multiple System Atrophy (MSA) and related Parkinsonian disorders. Alterity is preparing to initiate a Phase 3 pivotal trial in MSA, a rare and rapidly progressive disease. ATH434, the Company’s lead asset, has demonstrated clinically meaningful efficacy in a randomized, double-blind, placebo-controlled Phase 2 clinical trial in participants with MSA. Alterity has further reported positive data in its open label Phase 2 clinical trial in participants with 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 Company’s website at https://alteritytx.com.


Authorisation & Additional information
This announcement was authorized by David Stamler, CEO of Alterity Therapeutics Limited.

Contacts:

Investors
Elyse Shapiro
[email protected]

Remy Bernarda
Investor Relations Advisory Solutions
[email protected]
+1 (415) 203-6386

Media
Melissa Tempra
NWR Communications
[email protected]

Casey McDonald
Tiberend Strategic Advisors, Inc.
[email protected]
+1 (646) 577-8520

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.


Risks

  • Risks associated with drug development including potential delays or failures in clinical trials of ATH434.
  • Regulatory uncertainties related to approval processes for novel therapies in neurodegenerative diseases.
  • Financial risks concerning securing additional financing to support ongoing and future clinical trials and development activities.

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