Press Releases October 9, 2026 07:05 AM

Alterity Therapeutics to Present at the Canaccord Genuity Drug and Device Conference

Alterity Therapeutics to Present at Canaccord Genuity Drug and Device Conference, Highlighting Progress in Neurodegenerative Disease Treatments

By Hana Yamamoto
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Alterity Therapeutics, a clinical-stage biotechnology company focused on developing treatments for neurodegenerative diseases like Multiple System Atrophy (MSA), announced that its CEO, Dr. David Stamler, will present at the Canaccord Genuity Drug and Device Conference. The company is preparing to initiate a Phase 3 pivotal trial for its lead drug candidate ATH434, which has shown promising efficacy in Phase 2 clinical trials.

Alterity Therapeutics to Present at the Canaccord Genuity Drug and Device Conference
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Key Points

  • Alterity Therapeutics is advancing to a Phase 3 pivotal trial for ATH434 targeting Multiple System Atrophy, a rare neurodegenerative disorder.
  • CEO to deliver corporate presentation and engage with investors at a prominent drug and device industry conference.
  • The company is leveraging a broad drug discovery platform to develop disease-modifying therapies for neurological diseases, potentially impacting the biotechnology and pharmaceutical sectors.

MELBOURNE, Australia and SAN FRANCISCO, Oct. 09, 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 Canaccord Genuity Drug and Device Conference on Monday, October 12, 2026 at 3:50 p.m. AEST in Australia.

At the conference, Dr. Stamler will deliver a corporate presentation and will also host roundtable discussions with investors.

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


Risks

  • Clinical trial outcomes for ATH434 in Phase 3 are uncertain and may impact the company's program success.
  • MSA and related neurodegenerative diseases represent a rare condition market, which may present challenges in patient recruitment and commercial scalability.
  • Regulatory approvals for new therapies in neurodegenerative diseases carry inherent risks that may affect product launch timelines and market access.

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