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ATHE Overview

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Intellectia

Loading chart...

High
4.760
Open
4.650
VWAP
4.72
Vol
22.13K
Mkt Cap
82.29M
Low
4.650
Amount
104.44K
EV/EBITDA(TTM)
--
Total Shares
18.13M
EV
59.65M
EV/OCF(TTM)
--
P/S(TTM)
73.73
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.
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Events Timeline

(ET)
2026-04-27
07:40:00
Alterity Therapeutics Receives FDA Feedback, Advances ATH434 Phase 3 Development
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2026-04-22 (ET)
2026-04-22
07:40:00
Alterity Therapeutics Presents ATH434 Clinical Data
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2026-04-17 (ET)
2026-04-17
07:40:00
Alterity Therapeutics Appoints Ann Cunningham as Independent Director
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2026-03-30 (ET)
2026-03-30
07:40:00
Alterity Therapeutics Receives FDA Feedback to Advance ATH434 Phase 3 Development
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2026-03-04 (ET)
2026-03-04
07:30:00
Alterity Therapeutics Appoints Daniel Claassen as Chief Medical Advisor
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2026-01-30 (ET)
2026-01-30
07:30:00
Alterity Therapeutics Releases December 2025 Quarterly Cash Flow Report
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2026-01-21 (ET)
2026-01-21
07:30:00
Alterity Therapeutics Aims to Advance ATH434 into Phase 3 in 2026
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2025-11-10 (ET)
2025-11-10
07:56:15
Alterity Therapeutics Shares Findings on OH from ATH434-201 Trial
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News

Newsfilter
8.5
04-27Newsfilter
Alterity Receives Positive FDA Feedback, Advancing ATH434 Phase 3 Development
  • Positive FDA Feedback: Alterity Therapeutics received positive feedback during a Type C meeting with the FDA, confirming alignment on the chemistry, manufacturing, and control (CMC) elements of its Phase 3 development program for Multiple System Atrophy (MSA), marking a significant advancement in the company's pivotal clinical trial preparations.
  • Phase 3 Trial Readiness: The FDA endorsed Alterity's plans for the manufacturing and testing of ATH434, laying the groundwork for its Phase 3 trial, which, if approved, could facilitate commercialization, demonstrating the company's confidence and commitment to developing disease-modifying therapies.
  • Clinical Trial Progress: ATH434 has shown clinically meaningful efficacy in a randomized, double-blind, placebo-controlled Phase 2 trial, and positive data from an open-label Phase 2 trial further enhances its market potential in the treatment of MSA.
  • Future Planning: Alterity is set to hold an End-of-Phase 2 meeting with the FDA in mid-2026 to ensure the smooth initiation of the Phase 3 trial, indicating a clear strategic vision and ongoing regulatory compliance in its future clinical development.
Newsfilter
9.0
04-22Newsfilter
ATH434 Shows Efficacy in Multiple System Atrophy
  • Clinical Trial Results: In the Phase 2 trial for Multiple System Atrophy (MSA), ATH434 demonstrated a reduction in functional decline at Week 52 compared to placebo, with treatment effects of -1.9 points at 75 mg and -4.0 points at 50 mg (p=0.034), indicating a relative treatment effect of 41%, showcasing its potential in MSA treatment.
  • New Assessment Tool: The efficacy of ATH434 was validated using the MuSyCA composite scale, which integrates daily living activities and motor assessments, showing high sensitivity with placebo participants worsening by approximately 9.7 points over 52 weeks, confirming its effectiveness in clinical trials.
  • Future Development Direction: Alterity is preparing to initiate a Phase 3 pivotal trial in MSA, with positive results from ATH434 reinforcing its foundation as a disease-modifying therapy, potentially transforming treatment prospects for MSA patients.
  • Regulatory Engagement: The data presentation supports engagement with regulators, strengthening ATH434's clinical profile and potentially accelerating its path to market, further advancing Alterity's strategic positioning in the neurodegenerative disease sector.
Newsfilter
5.0
04-17Newsfilter
Alterity Appoints New Director to Strengthen Strategy
  • New Board Member: Alterity Therapeutics appointed Ann Cunningham as an independent Non-Executive Director on April 17, 2026, enhancing the board's global commercial and strategic expertise to support the company's transition towards late-stage development in Multiple System Atrophy (MSA).
  • Extensive Industry Experience: Cunningham brings over 25 years of global pharmaceutical and biotechnology experience, having held senior roles at Eli Lilly and Teva Pharmaceuticals, where she shaped commercial strategies for neurodegenerative diseases, which is expected to provide valuable market insights for Alterity's ATH434 project.
  • Clinical Trial Advancement: Her appointment comes at a pivotal time as Alterity prepares to advance ATH434 into Phase 3 clinical trials, with expectations that her commercial leadership will help maximize the value of the company's pipeline and drive product commercialization.
  • Patient-Focused Strategy: Cunningham expressed excitement about joining Alterity at this critical juncture, emphasizing the company's potential to address significant unmet needs in MSA, indicating her intention to leverage her experience to support the next phase of growth for the company.
Newsfilter
8.5
04-15Newsfilter
Alterity Announces KOL Event Focused on MSA Treatment
  • KOL Event Announcement: Alterity Therapeutics will host a virtual KOL event on April 28, 2026, featuring Dr. Roy Freeman from Harvard Medical School and Dr. Daniel Claassen from Vanderbilt University to discuss the treatment landscape of Multiple System Atrophy (MSA), aiming to raise awareness of this rare disease.
  • ATH434 Candidate Overview: Alterity's lead candidate, ATH434, is considered a potential first-in-class disease-modifying therapy, having demonstrated clinically meaningful efficacy in a randomized, double-blind Phase 2 trial, which could provide new treatment options for MSA patients.
  • Phase 2 Data Review: The event will review Phase 2 clinical trial data for ATH434, offering new insights and analyses that will help attendees better understand the drug's potential and its application in MSA treatment.
  • Phase 3 Planning Overview: Alterity will also outline its planned Phase 3 clinical trial, marking a significant step in advancing MSA treatment and potentially paving the way for future drug approvals.
Newsfilter
9.0
03-30Newsfilter
Alterity Receives Positive FDA Feedback to Advance Phase 3 Trial for MSA
  • FDA Meeting Outcome: Alterity Therapeutics received positive feedback from the FDA during a Type C meeting, confirming alignment on readiness for its Phase 3 clinical trial in Multiple System Atrophy (MSA), marking a significant milestone in the drug development process.
  • Clinical Development Plan: The planned Phase 3 trial will build on positive data from its Phase 2 clinical trials, where ATH434 demonstrated significant efficacy in randomized, double-blind studies, establishing a solid foundation for subsequent clinical testing.
  • Future Discussion Preparation: Alterity aims to reach agreement with the FDA on Chemistry, Manufacturing, and Controls (CMC) and the Phase 3 trial design, with today's favorable outcome paving the way for an End-of-Phase 2 meeting scheduled for mid-2026.
  • Strategic Implications: The FDA's support not only enhances Alterity's market competitiveness in the neurodegenerative disease sector but also instills confidence in the company's long-term growth prospects in the MSA field, potentially attracting more investor interest in its future developments.
NASDAQ.COM
9.0
03-30NASDAQ.COM
Alterity Receives Positive FDA Feedback for ATH434 Phase 3 Program
  • Regulatory Feedback Positive: Alterity Therapeutics received positive feedback from the FDA during a Type C Meeting, supporting its planned Phase 3 development program for ATH434 in Multiple System Atrophy (MSA), indicating confidence in clinical trial readiness.
  • Clinical Plan Confirmation: The FDA's written feedback addressed both clinical pharmacology and non-clinical development aspects, further confirming Alterity's strategic direction in advancing to the next stage of clinical testing, enhancing investor confidence in its R&D capabilities.
  • Multidisciplinary Strategy Implementation: This meeting is part of Alterity's multidisciplinary strategy to ensure alignment with the FDA for the smooth initiation of a pivotal Phase 3 trial, demonstrating the company's forward-looking planning in drug development.
  • Stable Market Performance: On the Australian Securities Exchange, ATH.AX traded at A$0.0080, unchanged from the previous session, reflecting a cautiously optimistic market sentiment regarding the company's future developments.

Valuation Metrics

The current forward P/E ratio for Alterity Therapeutics Ltd (ATHE.O) is 0.00, compared to its 5-year average forward P/E of -20.25. For a more detailed relative valuation and DCF analysis to assess Alterity Therapeutics Ltd's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
-20.25
Current PE
0.00
Overvalued PE
84.60
Undervalued PE
-125.10

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
-1.00
Current EV/EBITDA
-9.47
Overvalued EV/EBITDA
0.71
Undervalued EV/EBITDA
-2.71

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PS
11.32
Current PS
79.91
Overvalued PS
23.81
Undervalued PS
-1.17

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Frequently Asked Questions

What is Alterity Therapeutics Ltd (ATHE) stock price today?

The current price of ATHE is 4.75 USD — it has increased 4.63

What is Alterity Therapeutics Ltd (ATHE)'s business?

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.

What is the price predicton of ATHE Stock?

Wall Street analysts forecast ATHE stock price to fall over the next 12 months. According to Wall Street analysts, the average 1-year price target for ATHE is USD with a low forecast of USD and a high forecast of USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Alterity Therapeutics Ltd (ATHE)'s revenue for the last quarter?

Alterity Therapeutics Ltd revenue for the last quarter amounts to NaN USD, decreased

What is Alterity Therapeutics Ltd (ATHE)'s earnings per share (EPS) for the last quarter?

Alterity Therapeutics Ltd. EPS for the last quarter amounts to USD, decreased

How many employees does Alterity Therapeutics Ltd (ATHE). have?

Alterity Therapeutics Ltd (ATHE) has 9 emplpoyees as of May 01 2026.

What is Alterity Therapeutics Ltd (ATHE) market cap?

Today ATHE has the market capitalization of 82.29M USD.