# Alterity (ATHE) — News

ATHE · NASDAQ · Stock

Canonical page: https://www.lighthorse.io/tickers/athe/news

## Recent headlines

- [Alterity Therapeutics Limited: Ath434 50mg slowed MSA functional decline by about 52% vs placebo at week 52 - SEC filing](https://www.ainvest.com/news/alterity-therapeutics-limited-ath434-50mg-slowed-msa-functional-decline-52-placebo-week-52-sec-filing-2610) — AInvest Wire, Oct 5, 2026
  Alterity Therapeutics Limited (ASX: ATH, NASDAQ: ATHE) reported clinical results for its Phase 2 trial of ATH434 in patients with Multiple System Atrophy (MSA) in a recent SEC filing. The trial evaluated the efficacy of ATH434 at two dose levels (50 mg and 75 mg) compared to placebo over a 52-week…
- [Alterity Therapeutics receives FDA end-of-Phase 2 meeting minutes confirming registrational pathway for ATH434 in multiple system atrophy](https://www.ainvest.com/news/alterity-therapeutics-receives-fda-phase-2-meeting-minutes-confirming-registrational-pathway-ath434-multiple-system-atrophy-2607-59) — AInvest Wire, Jul 7, 2026
- [Alterity Therapeutics: receives FDA end-of-phase 2 meeting minutes confirming registrational pathway for ATH434 in multiple system atrophy](https://www.ainvest.com/news/alterity-therapeutics-receives-fda-phase-2-meeting-minutes-confirming-registrational-pathway-ath434-multiple-system-atrophy-2607) — AInvest Wire, Jul 7, 2026
  Alterity Therapeutics has received minutes from its recent end-of-phase 2 meeting with the U.S. Food and Drug Administration (FDA), confirming a potential registrational pathway for ATH434 in the treatment of multiple system atrophy (MSA), a rare and progressive neurodegenerative disorder. The…
- [Alterity Therapeutics Ltd-FDA meeting minutes confirm registrational path for ATH434](https://www.ainvest.com/news/alterity-therapeutics-fda-meeting-minutes-confirm-registrational-path-ath434-2607) — AInvest Wire, Jul 6, 2026
  Alterity Therapeutics Ltd. (ASX: ATH, NASDAQ: ATHE) has confirmed a clear regulatory pathway for its lead drug candidate, ATH434, following a successful End-of-Phase 2 (EOP2) meeting with the U.S. Food and Drug Administration (FDA). The meeting, held on June 9, 2026, aligned the company and the FDA…
- [Alterity Therapeutics reports successful end-of-Phase 2 meeting with FDA](https://www.ainvest.com/news/alterity-therapeutics-reports-successful-phase-2-meeting-fda-2606) — AInvest Wire, Jun 9, 2026

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