News
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Alterity Therapeutics provides corporate update
TipRanks · 01/30 12:38
Alterity Therapeutics: Appendix 4C – Q2 FY26 Quarterly Cash Flow Report & Corporate Update
Barchart · 01/30 06:25
Alterity Sharpens ATH434 Phase 3 Plans as Phase 2 MSA Data Strengthen
TipRanks · 01/30 03:49
Alterity Therapeutics highlights key 2026 objectives
TipRanks · 01/21 12:36
Alterity Therapeutics Issues Shareholder Letter Highlighting 2025 Progress and Key Objectives for 2026
Barchart · 01/21 06:25
Alterity Therapeutics Advances Lead MSA Drug Toward Phase 3 After Strong Phase 2 Data
TipRanks · 01/21 00:08
Alterity Therapeutics Issues 18 Million Unlisted Options Under Employee Scheme
TipRanks · 01/15 01:33
Alterity Flags Risk Context for Forward-Looking Statements in 2026 Presentation
TipRanks · 01/13 00:18
Alterity Therapeutics Options Lapse, Removing Potential Dilution Overhang
TipRanks · 01/07 00:37
Alterity Therapeutics initiated with a Speculative Buy at Canaccord
TipRanks · 12/17/2025 12:20
Canaccord Genuity Sticks to Their Buy Rating for Alterity Therapeutics (PRNAF)
TipRanks · 12/17/2025 06:05
Alterity Therapeutics Appoints New Director with No Initial Securities Interest
TipRanks · 11/24/2025 05:37
Alterity Therapeutics Announces New Director Appointment and Securities Interests
TipRanks · 11/24/2025 05:28
Alterity Therapeutics Announces Director Change
TipRanks · 11/24/2025 03:37
Alterity Therapeutics Announces Director Departure
TipRanks · 11/24/2025 03:28
Alterity Therapeutics CEO Outlines Strategic Vision
TipRanks · 11/21/2025 01:07
Alterity Therapeutics Advances in Neurodegenerative Disease Treatment
TipRanks · 11/21/2025 00:57
Alterity Therapeutics Announces Board Restructuring for Growth
TipRanks · 11/20/2025 23:28
Alterity ‘never lost sight’ of interest in Parkinson’s disease, CEO says
TipRanks · 11/20/2025 19:05
Alterity CEO says to meet with FDA, move forward with Phase 3 study
TipRanks · 11/20/2025 19:05
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About PRNAF
Alterity Therapeutics Limited is an Australia-based clinical-stage biotechnology company. The Company is focused on developing disease modifying treatments for neurodegenerative diseases. The Company's lead asset, ATH434, is to treat various Parkinsonian disorders. ATH434 is an oral agent designed to inhibit the aggregation of pathological proteins implicated in neurodegeneration. It has the potential to treat Parkinson's disease, as well as various Parkinsonian disorders, such as Multiple System Atrophy (MSA). The Company also has a drug discovery platform generating patentable chemical compounds to intercede in disease processes. Its lead asset, ATH434, is in a randomized, double blind, placebo-controlled Phase II clinical trial in participants with MSA. The Company is also conducting various nonclinical studies with ATH434 for use in Parkinson’s disease based on imaging of brain iron, preservation of neurons, and improvements in motor performance.