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Alterity Therapeutics prepares phase‑III study of ATH434 in multiple system atrophy
Alterity Therapeutics presented phase‑II data on ATH434 that the company says slowed progression of multiple system atrophy (MSA) versus placebo by 34–46%. The firm has agreed with the FDA on the study design, the primary endpoint (UMSARS) and a dose of 50 mg twice daily, and plans a randomized 12‑month phase‑III study with around 200 patients. Secondary endpoints, biomarkers and imaging also signal positive effects, and the safety profile was comparable to placebo. Management sees large commercial potential given the lack of an approved therapy and orphan/priority status (conservatively estimated peak sales of USD 2.4bn), but warns of the usual late‑stage development risks given a market capitalization of about USD 80m. » More on de.investing.com
Alterity Therapeutics: study confirms QSM MRI can detect iron deposits in MSA
A peer-reviewed study in NeuroImage shows that quantitative susceptibility mapping (QSM) can detect iron deposits in patients with multiple system atrophy (MSA). Analyses of data from the bioMUSE study found higher iron content in the lentiform nucleus in MSA patients; iron levels in the globus pallidus distinguished MSA from Parkinson with an accuracy of 0.76–0.79 and correlated with disease severity. Alterity has already used QSM in a Phase 2 study of ATH434 and is advancing development into a Phase 3 program; ATH434 has Fast Track and Orphan Drug status, and the company plans an end-of-Phase-2 meeting with the FDA in mid‑2026. Investor reaction: stock up 37.5% year-to-date, market capitalization about $86.5 million. » More on de.investing.com
Alterity Therapeutics: phase-2 data on ATH434 show slowing of MSA deterioration
Alterity Therapeutics presented positive phase-2 data on ATH434 at the AAN meeting, showing a slowing of functional decline in multiple system atrophy on the new MuSyCA scale (relative treatment effect up to 41% at 50 mg, p=0.034). Alternative analyses on the modified UMSARS‑I confirmed significant effects (up to 53% relative, p=0.029). The results recently pushed the share price markedly higher and the company is preparing a registration‑enabling phase‑3 trial; ATH434 has Fast‑Track and orphan‑drug status. » More on de.investing.com
Financials
| (EUR) | Dec 2025 | |
|---|---|---|
| Revenue | 0 | - |
| Gross profit | -32.9K | - |
| Net profit | -5.46M | - |
| EBITDA | -7.39M | - |
Fundamentals
| Metric | Value |
|---|---|
Market capitalization | €75.09M |
Number of shares | 217.51M |
52-week high/low | €0.47 - €0.000173 |
| Dividends | No |
Beta | -0.04 |
P/E ratio | -6.34 |
PEG ratio | -0.09 |
P/B ratio | 1.95 |
P/S ratio | 29.51 |
Company profile
Alterity Therapeutics Limited beschäftigt sich mit der Erforschung und Entwicklung von therapeutischen Medikamenten zur Behandlung der Alzheimer-Krankheit, der Huntington-Krankheit, der Parkinson-Krankheit und anderer neurologischer Erkrankungen in Australien. Der führende Medikamentenkandidat des Unternehmens ist ATH434, der die klinische Phase I zur Behandlung der Parkinson-Krankheit abgeschlossen hat. Darüber hinaus entwickelt es PBT2, das eine klinische Studie der Phase IIa zur Behandlung der Alzheimer-Krankheit abgeschlossen hat. Das Unternehmen war früher als Prana Biotechnology Limited bekannt und änderte im April 2019 seinen Namen in Alterity Therapeutics Limited. Alterity Therapeutics Limited wurde 1997 gegründet und hat seinen Hauptsitz in Melbourne, Australien.
| Name | Alterity Therapeutics |
| CEO | David A. Stamler |
| Headquarters | Melbourne,
vic Australia |
| Website | |
| Industry | Chemicals |
| IPO | 03/28/2000 |
| Employees | 9 |
Ticker symbols
| Exchange | Symbol |
|---|---|
Australian Securities Exchange Ltd | ATH.AX |
Pnk | PRNAF |
Frankfurt | PBN.F |
Düsseldorf | PBN.DU |
Hamburg | PBN.HM |
SIX | PBN.SW |
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