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Alterity Therapeutics (NASDAQ: ATHE) reports 2026 EGM outcomes

Filing Impact
(Neutral)
Filing Sentiment
(Neutral)
Form Type
6-K

Rhea-AI Filing Summary

Alterity Therapeutics Limited reports the results of its 2026 Extraordinary General Meeting, confirming that shareholders passed the resolutions presented at the meeting held on 29 May 2026.

The company is a clinical stage biotechnology business focused on disease-modifying therapies for Multiple System Atrophy and related Parkinsonian disorders. Its lead asset, ATH434, has shown clinically meaningful efficacy in a randomized, double-blind, placebo-controlled Phase 2 trial in MSA and additional positive data in an open label Phase 2 trial in advanced MSA. Alterity is preparing to initiate a Phase 3 pivotal trial in MSA and continues to develop a broader pipeline of patentable compounds targeting neurological disease pathology.

Positive

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Negative

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Extraordinary General Meeting date 29 May 2026 Date of Alterity Therapeutics’ 2026 EGM
Corporate law reference Section 251AA Corporations Act 2001 (Cth) section cited for EGM results
ASX listing rule reference 3.13.2 ASX Listing rule cited for disclosure of EGM resolutions
Extraordinary General Meeting financial
"resolutions passed by the shareholders of Alterity Therapeutics Limited at its Extraordinary General Meeting held on 29 May 2026"
Multiple System Atrophy medical
"The Company is focused on developing disease modifying therapies in Multiple System Atrophy (MSA) and related Parkinsonian disorders"
A progressive neurological disorder that damages multiple areas of the nervous system, causing problems with movement, balance and involuntary functions like blood pressure and bladder control; think of it as critical wiring in the body slowly failing. Investors care because the condition defines the size and urgency of the market for treatments, influences clinical trial difficulty and regulatory risk, and can lead to high per-patient pricing but also greater development uncertainty.
Phase 3 pivotal trial medical
"Alterity is preparing to initiate a Phase 3 pivotal trial in MSA, a rare and rapidly progressive disease"
A phase 3 pivotal trial is the large, final clinical study that tests whether a new drug or medical treatment works and is safe enough for regulators to approve it for widespread use. Think of it as the full-scale dress rehearsal before a product launches: positive results can unlock regulatory approval and big commercial upside, while failures can halt a program and significantly affect investor value.
randomized, double-blind, placebo-controlled Phase 2 clinical trial medical
"ATH434, the Company’s lead asset, has demonstrated clinically meaningful efficacy in a randomized, double-blind, placebo-controlled Phase 2 clinical trial"
open label Phase 2 clinical trial medical
"Alterity has further reported positive data in its open label Phase 2 clinical trial in participants with advanced MSA"
forward-looking statements regulatory
"This press release contains "forward-looking statements" within the meaning of section 27A of the Securities Act of 1933 and section 21E"
Forward-looking statements are predictions or plans that companies share about what they expect to happen in the future, like estimating sales or profits. They matter because they help investors understand a company's outlook, but since they are based on guesses and assumptions, they can sometimes be wrong.
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SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 6-K

 

REPORT OF FOREIGN PRIVATE ISSUER

PURSUANT TO RULE 13a-16 OR 15d-163

UNDER THE SECURITIES EXCHANGE ACT OF 1934

 

For the month of May 2026

 

Alterity Therapeutics Limited

(Name of Registrant)

 

Level 14, 350 Collins Street, Melbourne, Victoria 3000 Australia

(Address of Principal Executive Office)

 

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.

 

Form 20-F ☒       Form 40-F ☐

 

This Form 6-K is being incorporated by reference into our Registration Statement on Form S-8 (Files No. 333-251073, 333-248980 and 333-228671) and our Registration Statements on Form F-3 (Files No. 333-274816, 333-251647, 333-231417 and 333-250076)

 

 

 

 

ALTERITY THERAPEUTICS LIMITED

(a development stage enterprise)

 

The following exhibits are submitted:

 

99.1

Results of the Extraordinary Meeting of Shareholders held on 29 May 2026.

 

1

 

SIGNATURE

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

 

Alterity Therapeutics Limited

     
 

By:

/s/ Julian Babarczy

   

Julian Babarczy

   

Chairman

 

Date: May 29, 2026

2

Exhibit 99.1

 

 

 

alt.jpg

 

 

Results of 2026 Extraordinary General Meeting

 

 

MELBOURNE, AUSTRALIA AND SAN FRANCISCO, USA 29 May 2026: 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 in accordance with ASX Listing rule 3.13.2 and Section 251AA of the Corporations Act 2001 (Cth), the attached information is provided in relation to the resolutions passed by the shareholders of Alterity Therapeutics Limited at its Extraordinary General Meeting held on 29 May 2026.

 

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 authorised by the Board of Alterity Therapeutics Limited.

 

Contacts:

 

Investors:

Elyse Shapiro

ir@alteritytx.com

 

Remy Bernarda

Investor Relations Advisory Solutions

ir@alteritytx.com

+1 (415) 203-6386

 

 

 

Media

Casey McDonald

Tiberend Strategic Advisors, Inc.

cmcdonald@tiberend.com

+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 Companys 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 Companys 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 Companys 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.

 

 

 

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FAQ

What did Alterity Therapeutics (ATHE) announce in its May 2026 Form 6-K?

Alterity Therapeutics announced that shareholders passed the resolutions presented at its 2026 Extraordinary General Meeting held on 29 May 2026. The filing also reiterates the company’s clinical focus on Multiple System Atrophy and highlights progress of its lead drug candidate, ATH434, in Phase 2 trials.

What is Alterity Therapeutics’ lead drug candidate ATH434 targeting?

ATH434 is Alterity Therapeutics’ lead drug candidate targeting Multiple System Atrophy, a rare and rapidly progressive neurodegenerative disease. The company reports clinically meaningful efficacy in a randomized, double-blind, placebo-controlled Phase 2 trial, along with positive data from an open label Phase 2 trial in advanced MSA.

What clinical stage is Alterity Therapeutics’ MSA program in?

Alterity Therapeutics is preparing to initiate a Phase 3 pivotal trial in Multiple System Atrophy. This follows clinically meaningful efficacy results from a randomized, double-blind, placebo-controlled Phase 2 trial and additional positive outcomes from an open label Phase 2 study in participants with advanced MSA.

What type of company is Alterity Therapeutics (ATHE)?

Alterity Therapeutics is a clinical stage biotechnology company focused on developing disease-modifying treatments for neurodegenerative diseases. Its programs center on Multiple System Atrophy and related Parkinsonian disorders, supported by a drug discovery platform generating patentable chemical compounds aimed at underlying neurological disease pathology.

Where is Alterity Therapeutics based and on which exchanges is it listed?

Alterity Therapeutics is based in Melbourne, Australia, and San Francisco, California, USA. The company’s shares trade on the Australian Securities Exchange under the symbol ATH and on the NASDAQ under the symbol ATHE, reflecting its cross-border biotechnology operations and investor base.

What forward-looking statement risks does Alterity Therapeutics highlight?

Alterity highlights risks related to financing, development, testing, regulatory approval, production, and marketing of its drug candidates such as ATH434. It also notes uncertainties around side effects, therapeutic efficacy, patent protection, enforcing intellectual property rights, and overall freedom to operate within its chosen neurodegenerative disease markets.

Filing Exhibits & Attachments

1 document