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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 programMELBOURNE, Australia and SAN FRANCISCO, March 30, 2026 (GLOBE NEWSWIRE) -- Alterity Therapeutics (ASX: ATH, NASDAQ: ATHE) (“Alterity” or “the Company”), a biotechnology company dedicated to developing disease modifying treatments for neurodegenerative diseases, today announced it has received positive regulatory feedback following a Type C Meeting with the U.S. Food and Drug Administration (FDA) regarding its planned Phase 3

articleAlterity Therapeutics Ltd.March 30, 20263/company/alterity-therapeutics-ltd/news/alterity-therapeutics-receives-positive-fda-feedback-following-type-c-meeting-on-ath434-phase-3-program
Alterity Therapeutics Receives Positive FDA Feedback Following Type C Meeting on ATH434 Phase 3 Program

About this update from Alterity Therapeutics Ltd.

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More updates from Alterity Therapeutics Ltd.

the CompanyFood and Drug Administrationneurodegenerative diseasesPhase 3 trialMultiple System AtrophyAlterity