Alterity Therapeutics Limited (ASX:ATH)
| Market Cap | 130.50M +30.0% |
| Revenue (ttm) | 6.64M +78.2% |
| Net Income | -14.59M |
| EPS | -0.08 |
| Shares Out | 217.51M |
| PE Ratio | n/a |
| Forward PE | n/a |
| Dividend | n/a |
| Ex-Dividend Date | n/a |
| Volume | 417,387 |
| Open | 0.5900 |
| Previous Close | 0.5850 |
| Day's Range | 0.5600 - 0.6050 |
| 52-Week Range | 0.3500 - 0.8500 |
| Beta | -0.01 |
| Analysts | Strong Buy |
| Price Target | 2.28 (+280.0%) |
| Earnings Date | Jul 28, 2026 |
About Alterity Therapeutics
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 StatementsNews
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 Aligns With FDA On Phase 3 Design For ATH434 In Treating Multiple System Atrophy
(RTTNews) - Alterity Therapeutics (ATHE), a biotechnology company, on Tuesday reported achieving alignment with the U.S. Food and Drug Administration (FDA) on the planned Phase 3 trial for ATH434 in t...
Alterity Therapeutics (ATHE) Gets FDA Nod for Phase 3 Program
Alterity Therapeutics (ATHE) Gets FDA Nod for Phase 3 Program
Alterity Therapeutics (ATHE) Secures FDA Agreement for Phase 3 ATH434 Trial
Alterity Therapeutics (ATHE) Secures FDA Agreement for Phase 3 ATH434 Trial
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...
Alterity Therapeutics Receives Positive FDA Feedback Following Type C Meeting on ATH434 Phase 3 Program
Alignment reached on key elements of ATH434 Phase 3 development program Alignment reached on key elements of ATH434 Phase 3 development program
Alterity Therapeutics Transcript: NWR Virtual Healthcare Conference
ATH434 demonstrated robust efficacy in phase II for MSA, showing significant slowing of disease progression and strong safety. Commercial potential is high, with peak sales estimated at $2.4 billion and broad neurologist support. Phase III is planned globally, with key milestones expected this year.
Alterity Therapeutics to Participate in the Bell Potter Healthcare Horizons Summit
MELBOURNE, Australia and SAN FRANCISCO, March 09, 2026 (GLOBE NEWSWIRE) -- Alterity Therapeutics (ASX: ATH, NASDAQ: ATHE) (“Alterity” or “the Company”), a biotechnology company dedicated to developing...