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| Date | Price Target | Rating | Analyst |
|---|---|---|---|
| 6/16/2026 | $10.00 | Buy | Ladenburg Thalmann |
| 2/3/2025 | Speculative Buy → Hold | The Benchmark Company | |
| 12/12/2024 | $8.00 | Buy | Maxim Group |
| 8/20/2021 | $4.00 | Speculative Buy | Benchmark |
Ladenburg Thalmann resumed coverage of Alterity Therapeutics with a rating of Buy and set a new price target of $10.00
The Benchmark Company downgraded Alterity Therapeutics from Speculative Buy to Hold
Maxim Group initiated coverage of Alterity Therapeutics with a rating of Buy and set a new price target of $8.00
MELBOURNE, Australia and SAN FRANCISCO, July 21, 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 participate in the BTIG Biotechnology Conference 2026 taking place virtually 28-29 July 2026. At the conference, Dr. Stamler will host 1-on-1 meetings with investors in the United States. About Alterity Therapeutics Limited Alterity Therapeutics is a clinical stage biotechnology company dedicated to creating an alternate future for people living with neurodeg
– Official FDA minutes confirm the previously announced End-of-Phase 2 meeting outcomes and provide additional detail on the planned Phase 3 protocol — – FDA agreed that a single pivotal Phase 3 trial plus confirmatory evidence could support an approval of ATH434 for the treatment of MSA – – Pivotal Phase 3 trial activities on track to initiate by year-end 2026 – MELBOURNE, Australia and SAN FRANCISCO, July 07, 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 it has received the official meeting minutes fr
– Successful End-of-Phase 2 meeting with FDA agreeing on key elements of the proposed Phase 3 design, including study population, dosing regimen, and treatment duration – – FDA agrees on UMSARS Part I as primary endpoint after ATH434 demonstrated 48% slowing of disease progression versus placebo in Phase 2 study – – FDA agrees with 50mg dose level which achieved clinically and statistically significant efficacy in Phase 2 study – – Pivotal Phase 3 trial activities on track to initiate by year-end 2026 – MELBOURNE, Australia and SAN FRANCISCO, June 09, 2026 (GLOBE NEWSWIRE) -- Alterity Therapeutics ((ASX: ATH, trading under the ASX code ATHDA until 12 June, NASDAQ:ATHE) ("Alterity" or
6-K - ALTERITY THERAPEUTICS LTD (0001131343) (Filer)
6-K - ALTERITY THERAPEUTICS LTD (0001131343) (Filer)
6-K - ALTERITY THERAPEUTICS LTD (0001131343) (Filer)
4 - ALTERITY THERAPEUTICS LTD (0001131343) (Issuer)
4 - ALTERITY THERAPEUTICS LTD (0001131343) (Issuer)
3 - ALTERITY THERAPEUTICS LTD (0001131343) (Issuer)
SC 13D/A - ALTERITY THERAPEUTICS LTD (0001131343) (Subject)
SC 13D/A - ALTERITY THERAPEUTICS LTD (0001131343) (Subject)
SC 13D/A - ALTERITY THERAPEUTICS LTD (0001131343) (Subject)
Highlights Aligned with the FDA in two Positive Type C meetings supporting key elements of the planned Phase 3 program for ATH434 in MSAAdvancing ATH434 toward pivotal Phase 3 program; on track for End-of-Phase 2 FDA meeting mid-year 2026Late breaking platform presentation at American Academy of Neurology annual meeting demonstrated consistent evidence of efficacy and reinforces ATH434's clinical profileStrengthened clinical leadership with appointment of Dr. Daniel Claassen as Chief Medical AdvisorEnhanced Board of Directors with appointment of Ms. Ann Cunningham, bringing extensive global commercial and neurodegenerative disease expertiseHosted a virtual KOL event featuring leading expe
MELBOURNE, Australia and SAN FRANCISCO, April 17, 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 the appointment of Ms Ann Cunningham to its Board of Directors as an independent Non-Executive Director, effective 17th April 2026. Ms Cunningham's appointment further strengthens Alterity's Board composition, adding significant global commercial and strategic expertise as the Company transitions toward late-stage development in Multiple System Atrophy (MSA). Ms Cunningham brings more than 25 years of global pharmac
MELBOURNE, Australia and SAN FRANCISCO, March 04, 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 Daniel O. Claassen, M.D., M.S., was appointed Chief Medical Advisor and will begin his role in March 2026. As a tenured professor, Dr. Claassen will also retain his academic appointment at Vanderbilt University Medical Center. Dr. Claassen is a board-certified neurologist and internationally recognized expert in neurodegenerative diseases, with more than two decades of clinical and translational research in mov