$VTGN

Vistagen Therapeutics, Inc.

Vistagen Therapeutics is a clinical-stage therapeutics company developing medicines for patients with social anxiety disorder, depression, menopausal hot flashes, psychomotor impairment due to mental fatigue, and cancer cachexia. Its neuroscience pipeline includes five intranasal pherine candidates: fasedienol for social anxiety disorder, itruvone for major depressive disorder, refisolone for menopausal hot flashes, PH15 for psychomotor impairment due to mental fatigue, and PH284 for cancer cachexia. The candidates are designed to act through nasal neurocircuits. Vistagen is also developing AV-101, an oral prodrug candidate targeting the N-methyl-D-aspartate receptor for potential treatment of neurological disorders. Its business centers on developing its product candidates, with potential commercialization described as a goal. Vistagen is headquartered in South San Francisco, California.

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Vistagen Therapeutics, Inc. implemented a Board-approved reduction in workforce by approximately 31%, retaining core clinical, regulatory, technical, and…

Vistagen Therapeutics, Inc. (VTGN) filed an SEC Form 8-K — Other Events. Item 2.05 Costs Associated with Exit or Disposal Activities On October 26, 2026, Vistagen Therapeutics, Inc. (the “ Company ”) implemented a Board-approved reduction in workforce by approximately 31%, retaining core clinical, regulatory, technical, and corporate capabilities requ

VTGN Q2'26 Earnings: revenue estimate is 500.00K USD

Vistagen Therapeutics (VTGN) will report Q2'26 earnings on November 5. Analysts expect revenue of 500,000 USD and a loss of 0.38 USD per share. The announcement is scheduled for 7:00 AM ET.

Vistagen partners with GATC Health on AI drug development

Vistagen (VTGN) partners with GATC Health to use AI and predictive modeling for its drug development programs. The collaboration focuses on fasedienol for social anxiety, itruvone for depression, and refisolone for menopausal symptoms. GATC Health's technology aims to enhance protocol development and resource allocation.

VTGN sentiment & insider activity

Over the past 7 days, AlphAI's AI scored 2 news stories mentioning VTGN (Vistagen Therapeutics, Inc.). Coverage has been balanced: 0 bullish, 2 neutral, and 0 bearish.

Recent VTGN coverage spans corporate actions, earnings and financial news.

What's driving VTGN

AlphAI scores every news story that mentions VTGN with an AI model for sentiment and relevance, and aggregates insider trades from Vistagen Therapeutics, Inc.'s SEC EDGAR Form 4 filings. Figures refresh continuously.

News on $VTGN

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Vistagen Therapeutics, Inc. implemented a Board-approved reduction in workforce by approximately 31%, retaining core clinical, regulatory, technical, and…

Vistagen Therapeutics, Inc. (VTGN) filed an SEC Form 8-K — Other Events. Item 2.05 Costs Associated with Exit or Disposal Activities On October 26, 2026, Vistagen Therapeutics, Inc. (the “ Company ”) implemented a Board-approved reduction in workforce by approximately 31%, retaining core clinical, regulatory, technical, and corporate capabilities requ

$VTGNLow

Vistagen partners with GATC Health on AI drug development

Vistagen (VTGN) partners with GATC Health to use AI and predictive modeling for its drug development programs. The collaboration focuses on fasedienol for social anxiety, itruvone for depression, and refisolone for menopausal symptoms. GATC Health's technology aims to enhance protocol development and resource allocation.

Vistagen Therapeutics, Inc. (VTGN): Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers

Vistagen Therapeutics, Inc. (VTGN) filed an SEC Form 8-K — Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers. Item 5.02 Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers; Compensatory Arrangements of Certain Officers. Amendment and Restatement of Executive Severance Plan On October 7, 2026, the Board of Directors (the “ Board ”) of Vistage

$VTGNMedAI 8/10

Vistagen Reports Positive Findings Supporting Fasedienol’s Potential in Very Severe Social Anxiety Disorder

Vistagen Therapeutics, Inc. (VTGN) filed an SEC Form 8-K — Other Events. EXHIBIT 99.1 Vistagen Reports Positive Findings Supporting Fasedienol’s Potential in Very Severe Social Anxiety Disorder Exploratory research results presented at Psych Congress 2026 in New Orleans Full poster presentation can be found on “Publications” section of Company’s websi

$VTGNMedAI 8/10

Vistagen Announces Preliminary Positive Data from Open-Label Extension Portion of PALISADE-4 Phase 3 Study of Fasedienol for the Acute Treatment of Social…

Vistagen Therapeutics, Inc. (VTGN) filed an SEC Form 8-K — Other Events. EXHIBIT 99.1 Vistagen Announces Preliminary Positive Data from Open-Label Extension Portion of PALISADE-4 Phase 3 Study of Fasedienol for the Acute Treatment of Social Anxiety Disorder Fasedienol nasal spray was well-tolerated in patients with social anxiety disorder with no new

$VTGNLow

Vistagen Therapeutics, Inc. (VTGN): Submission of Matters to a Vote of Security Holders

Vistagen Therapeutics, Inc. (VTGN) filed an SEC Form 8-K — Submission of Matters to a Vote of Security Holders. Item 5.07 Submission of Matters to a Vote of Security Holders. On September 10, 2026, Vistagen Therapeutics, Inc. (the “ Company ”) held its 2026 Annual Meeting of Stockholders (the “ 2026 Annual Meeting ”). At the 2026 Annual Meeting, as set forth below, the Company’s stockholde

$VTGNMed

Vistagen Reports Fiscal Year 2027 First Quarter Financial Results and Corporate Update

Vistagen Therapeutics, Inc. (VTGN) filed an SEC Form 8-K — Results of Operations and Financial Condition. Exhibit 99.1 Vistagen Reports Fiscal Year 2027 First Quarter Financial Results and Corporate Update Exploratory analyses of patients with very severe social anxiety disorder demonstrated nominally statistically significant improvement in recently reported clinical studies FDA eng

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