Alterity Therapeutics Limited Stock Nasdaq

Equities

ATHE

US02155X2053

Biotechnology & Medical Research

Delayed Nasdaq 03:31:16 2024-04-25 pm EDT 5-day change 1st Jan Change
2.28 USD -2.15% Intraday chart for Alterity Therapeutics Limited +6.54% -8.43%
Sales 2024 * 1.87M Sales 2025 * 1.39M Capitalization 20.39M
Net income 2024 * -8M Net income 2025 * -10M EV / Sales 2024 * 10.9 x
Net cash position 2024 * - Net cash position 2025 * - EV / Sales 2025 * 14.7 x
P/E ratio 2024 *
-
P/E ratio 2025 *
-
Employees -
Yield 2024 *
-
Yield 2025 *
-
Free-Float 86.93%
More Fundamentals * Assessed data
Dynamic Chart

Latest transcript on Alterity Therapeutics Limited

1 day-2.15%
1 week+6.54%
Current month+10.14%
1 month+33.33%
3 months+13.45%
6 months-8.43%
Current year-8.43%
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1 week
2.00
Extreme 2
2.50
1 month
1.71
Extreme 1.71
3.19
Current year
1.55
Extreme 1.55
3.19
1 year
1.55
Extreme 1.55
5.41
3 years
1.55
Extreme 1.55
27.50
5 years
1.55
Extreme 1.55
51.50
10 years
1.55
Extreme 1.55
176.40
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Managers TitleAgeSince
Chief Executive Officer 63 17-04-30
Founder 69 97-11-10
Director of Finance/CFO 64 14-04-30
Members of the board TitleAgeSince
Founder 69 97-11-10
Director/Board Member 68 05-07-28
Director/Board Member 45 11-08-07
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Date Price Change Volume
24-04-25 2.28 -2.15% 22 144
24-04-24 2.33 +9.39% 173,935
24-04-23 2.13 0.00% 33,202
24-04-22 2.13 +4.41% 43,741
24-04-19 2.04 -4.67% 54,226

Delayed Quote Nasdaq, April 25, 2024 at 03:31 pm EDT

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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. ATH434 has been granted Orphan designation for the treatment of MSA. The Phase 2 clinical trial is a randomized, double-blind, placebo-controlled investigation of ATH434 in patients with early-stage MSA.
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Quarterly revenue - Rate of surprise