Alterity Therapeutics Limited (ATHE)
| Market Cap | 96.07M +181.7% |
| Revenue (ttm) | 4.43M +78.2% |
| Net Income | -9.73M |
| EPS | -0.06 |
| Shares Out | 217.51M |
| PE Ratio | n/a |
| Forward PE | n/a |
| Dividend | n/a |
| Ex-Dividend Date | n/a |
| Volume | 5,818 |
| Open | 5.47 |
| Previous Close | 5.38 |
| Day's Range | 5.38 - 5.55 |
| 52-Week Range | 2.66 - 7.00 |
| Beta | -0.03 |
| Analysts | Strong Buy |
| Price Target | 12.67 (+133.33%) |
| Earnings Date | Jul 28, 2026 |
About ATHE
Alterity Therapeutics Limited is engages in research and development of Parkinsonian and neurodegenerative disorders, including Multiple System Atrophy (MSA) and Parkinson’s disease. The company’s lead drug candidate is ATH434, a small molecule drug candidate that has completed Phase II clinical trial for the treatment of Parkinson’s disease. It is also developing ATH434-201, which is in Phase II clinical trial to treat multiple system atrophy early stage; and ATH434-202 that is in Phase II clinical trial to treat multiple system atrophy, as we... [Read more]
Financial Performance
In fiscal year 2025, Alterity Therapeutics's revenue was 5.44 million, an increase of 35.32% compared to the previous year's 4.02 million. Losses were -12.15 million, -36.48% less than in 2024.
Financial numbers in AUD Financial StatementsAnalyst Summary
According to 3 analysts, the average rating for ATHE stock is "Strong Buy." The 12-month stock price target is $12.67, which is an increase of 133.33% from the latest price.
News
Alterity To Initiate Phase 3 Trial Of ATH434 In MSA Subsequent To Receipt Of EOP2 Minutes From FDA
(RTTNews) - Alterity Therapeutics Ltd. (ATHE), a clinical-stage biotechnology company, announced that it has received the U.S. Food and Drug Administration's meeting minutes from the End-of Phase 2 or...
Alterity Therapeutics (ATHE) Faces 8.8% Decline Ahead of Market Open
Alterity Therapeutics (ATHE) Faces 8.8% Decline Ahead of Market Open
Alterity Therapeutics (ATHE) Advances Towards Phase 3 Trial Approval
Alterity Therapeutics (ATHE) Advances Towards Phase 3 Trial Approval
Alterity Therapeutics receives FDA meeting minutes on pathway for ATH434
Alterity Therapeutics (ATHE) announced that it has received the official meeting minutes from its End-of Phase-2 meeting for ATH434 in Multiple System Atrophy from the FDA. The minutes confirm the…
Alterity Therapeutics Receives FDA End-of-Phase 2 Meeting Minutes Confirming Registrational Pathway for ATH434 in Multiple System Atrophy
– Official FDA minutes confirm the previously announced End-of-Phase 2 meeting outcomes and provide additional detail on the planned Phase 3 protocol —
Alterity Therapeutics initiated with a Buy at JonesResearch
JonesResearch initiated coverage of Alterity Therapeutics (ATHE) with a Buy rating and $16 price target Alterity’s oral iron chaperone, ATH434, is set to enter Phase 3 development for multiple system…
Alterity Therapeutics assumed with a Buy at Ladenburg
Ladenburg analyst Caroline Palomeque assumed coverage of Alterity Therapeutics (ATHE) with a Buy rating and $10 price target Alterity is entering late-stage clinical development which “is an ideal tim...
Alterity Therapeutics Slides: Corporate presentation
Alterity Therapeutics has posted slides in relation to its latest quarterly earnings report, which was published on June 15, 2026.
Alterity Therapeutics achieves alignment with FDA on program for ATH434 in MSA
Alterity Therapeutics (ATHE) announced the outcome of its End-of-Phase 2 meeting with the FDA, achieving alignment on the elements of the company’s registrational Phase 3 program for ATH434 in Multipl...
Alterity Therapeutics Achieves Alignment with U.S. FDA on Pivotal Phase 3 Program for ATH434 in Multiple System Atrophy
– 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 –
Alterity Therapeutics management to meet with BTIG
Meeting to be held in San Francisco on June 10-11 hosted by BTIG.
Alterity Therapeutics Data Presentations Support Advancement of ATH434 into Phase 3 in Multiple System Atrophy
– Alterity's novel imaging and biomarker approach positions the Company at the forefront of clinical research in MSA –
Alterity Therapeutics publishes quantitative susceptibility mapping MRI data
Alterity Therapeutics (ATHE) announced the publication of a peer-reviewed study in NeuroImage, demonstrating that quantitative susceptibility mapping MRI can detect disease-specific iron accumulation ...
Alterity Therapeutics Announces Publication Demonstrating the Utility of Quantitative MRI as a Biomarker for Multiple System Atrophy
– Peer-reviewed study from the bioMUSE Natural History Study shows advanced MRI method detects disease-specific iron accumulation that supports diagnosis and correlates with clinical severity in patie...
Alterity Therapeutics to Deliver Presentations at Multiple Medical Conferences in May 2026
MELBOURNE, Australia and SAN FRANCISCO, May 07, 2026 (GLOBE NEWSWIRE) -- Alterity Therapeutics (ASX: ATH, NASDAQ: ATHE) (“Alterity” or “the Company”), a biotechnology company dedicated to developing d...
Alterity Therapeutics Releases Appendix 4C – Q3 FY26 Quarterly Cash Flow Report & Corporate Update
Highlights Aligned with the FDA in two Positive Type C meetings supporting key elements of the planned Phase 3 program for ATH434 in MSA Advancing ATH434 toward pivotal Phase 3 program; on track for E...
Alterity Therapeutics Earnings release: Q3 2026
Alterity Therapeutics released its Q3 2026 earnings on April 29, 2026, summarizing the period's financial results.
Alterity Therapeutics Transcript: KOL event
ATH434 demonstrated up to 48% slowing of MSA progression in phase II with a strong safety profile, supported by robust biomarker and imaging data. The upcoming phase III trial will use a 50 mg dose, rigorous patient selection, and validated endpoints, with regulatory alignment and key catalysts expected in 2026.
Alterity Therapeutics receives FDA feedback after second ATH434 Type C meeting
Alterity Therapeutics (ATHE) announced it has received regulatory feedback following a Type C meeting with the FDA regarding its planned Phase 3 development program for ATH434 in Multiple System Atrop...
Alterity Therapeutics Receives Positive FDA Feedback Following Second Type C Meeting on ATH434 Phase 3 Program in Multiple System Atrophy
MELBOURNE, Australia and SAN FRANCISCO, April 27, 2026 (GLOBE NEWSWIRE) -- Alterity Therapeutics (ASX: ATH, NASDAQ: ATHE) (“Alterity” or “the Company”), a biotechnology company dedicated to developing...
Alterity Therapeutics presents new data analyses from ATH434 trial
Alterity Therapeutics (ATHE) announced the presentation of new data analyses from the Phase 2 trial of ATH434, demonstrating clinical efficacy in patients with Multiple System Atrophy. The analysis wa...
Alterity Therapeutics Presents New Analysis of ATH434 Phase 2 Trial Data in Late Breaking Science Session of the American Academy of Neurology
- ATH434 reduced functional decline vs placebo at Week 52 on MuSyCA, a newly described MSA composite scale - - Effects seen on both daily function and neurological examination, consistent with previou...
Alterity Therapeutics appoints Cunningham to Board of Directors
Alterity Therapeutics (ATHE) announced the appointment of Ann Cunningham to its Board of Directors as an independent Non-Executive Director, effective 17th April 2026. Cunningham’s appointment further...
Alterity Therapeutics Appoints Highly Experienced Biotech Executive Ann Cunningham to its Board of Directors
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...
Alterity Therapeutics receives regulatory feedback from FDA regarding ATH434
Alterity Therapeutics (ATHE) announced it has received regulatory feedback following a Type C Meeting with the FDA regarding its planned Phase 3 development program for ATH434 in Multiple System Atrop...