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Alterity Therapeutics

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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. » Plus sur 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. » Plus sur 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. » Plus sur de.investing.com

Données financières de l'entreprise

Au dernier trimestre, Alterity Therapeutics a réalisé un chiffre d'affaires de 0 € et un bénéfice net de -5,46 M €
(EUR) déc. 2025
YoY
Chiffre d'affaires 0 -
Bénéfice brut -32,9 k -
Bénéfice net -5,46 M -
EBITDA -7,39 M -

Données fondamentales

Indicateur Valeur
Capitalisation boursière
75,09 M €
Nombre d'actions
217,51 M
Plus haut/bas sur 52 semaines
0,47 € - 0,000173 €
Dividendes Non
Bêta
-0,04
Ratio P/E
-6,34
Ratio PEG
-0,09
Ratio P/B
1,95
Ratio P/S
29,51

Profil de l'entreprise

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.

Nom
Alterity Therapeutics
PDG
David A. Stamler
Siège social Melbourne, vic
Australie
Site web
Industrie
Produits chimiques
Introduction en bourse
28/03/2000
Employés 9

Symboles boursiers

Bourse Symbole
Australian Securities Exchange Ltd
ATH.AX
Pnk
PRNAF
Frankfurt
PBN.F
Düsseldorf
PBN.DU
Hamburg
PBN.HM
SIX
PBN.SW

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