Welcome to our dedicated page for Vistagen Therapeutics SEC filings (Ticker: VTGN), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
The Vistagen Therapeutics, Inc. (Nasdaq: VTGN) SEC filings page on Stock Titan provides access to the company’s regulatory disclosures as filed with the U.S. Securities and Exchange Commission. Vistagen is a Nevada-incorporated, late clinical-stage biopharmaceutical company headquartered in South San Francisco, California, and its filings offer detailed insight into its nose-to-brain neurocircuitry platform, pherine pipeline, governance, and financial condition.
Through documents such as Form 10-K annual reports and Form 10-Q quarterly reports, readers can review Vistagen’s descriptions of its business as a neuroscience-focused biopharmaceutical company, its intranasal pherine product candidates, and the risks and uncertainties associated with late-stage clinical development. These filings also discuss the company’s focus on indications including social anxiety disorder, major depressive disorder, and vasomotor symptoms (hot flashes) due to menopause, as well as other women’s health conditions.
Current reports on Form 8-K provide timely information on material events, including clinical and corporate milestones. Recent 8-K filings have addressed topics such as financial results for specific fiscal quarters, progress in the PALISADE Phase 3 program for fasedienol in social anxiety disorder, and changes in executive leadership and board composition. Proxy materials on Form DEF 14A describe matters submitted to a shareholder vote, including director elections, advisory votes on executive compensation, and auditor ratification, along with details about governance practices.
Stock Titan’s platform enhances these filings with AI-powered summaries that highlight key points from lengthy documents, helping users quickly understand complex sections on clinical programs, compensation, and shareholder matters. Real-time updates from EDGAR ensure that new Vistagen filings, including any future Forms 4 reporting insider equity awards or transactions, appear promptly, while AI-generated overviews can assist in interpreting how each filing relates to the company’s pherine development strategy and late-stage clinical status.
Vistagen Therapeutics, Inc. reported a larger quarterly loss as it continues funding late-stage development of its intranasal pherine neuroscience pipeline. For the quarter ended December 31, 2025, revenue was $0.3 million, while research and development and general and administrative expenses rose to $14.2 million and $5.6 million, respectively, leading to a net loss of $18.9 million.
For the nine-month period, revenue reached $0.8 million and net loss widened to $53.4 million as the company advanced its Phase 3 PALISADE program for fasedienol in social anxiety disorder and progressed other pherine candidates. Cash, cash equivalents and marketable securities totaled $61.8 million, but management concluded there is substantial doubt about Vistagen’s ability to continue as a going concern beyond twelve months without additional financing. The company also received a Nasdaq notice for not meeting the $1.00 minimum bid price requirement.
Vistagen Therapeutics reported fiscal 2026 third quarter results showing higher spending as it advances late-stage neuroscience programs. Revenue was modest at $0.3 million, while research and development expense rose to $14.2 million from $11.3 million, and general and administrative expense increased to $5.6 million from $4.0 million. Net loss widened to $18.9 million compared with $14.1 million a year earlier.
Cash, cash equivalents, and marketable securities totaled $61.8 million as of December 31, 2025. The PALISADE-4 Phase 3 trial of fasedienol in social anxiety disorder is ongoing, with topline results from the randomized portion expected in the first half of 2026 after refinements informed by PALISADE-3, which did not meet its primary endpoint. The company is also preparing a U.S. IND filing in the first half of 2026 for refisolone (PH80) in menopausal hot flashes and has implemented cash preservation initiatives to support completing PALISADE-4 and advancing its pherine pipeline.
Vistagen Therapeutics, Inc. received a Nasdaq notice that its common stock no longer meets the Nasdaq Capital Market’s minimum $1.00 bid price requirement, after trading below that level for 30 consecutive business days. The notice does not immediately affect the stock’s Nasdaq listing.
To regain compliance, Vistagen’s closing bid price must reach at least $1.00 per share for 10 consecutive business days during the 180-day period from February 3, 2026 to August 3, 2026. If the company still does not comply, Nasdaq may grant a second 180-day period if other listing standards are met, after which the stock could be delisted if compliance is not restored.
The Vanguard Group filed an amended Schedule 13G reporting beneficial ownership of 1,824,738 shares of Vistagen Therapeutics Inc common stock, representing 4.62% of the class as of December 31, 2025. Vanguard reports no sole voting or dispositive power, with all voting and dispositive authority shared.
Vanguard states the shares are held in the ordinary course of business and not to change or influence control of Vistagen. The filing notes that Vistagen-related holdings are for Vanguard’s clients, and no single other person has more than a 5% interest in the reported securities. Vanguard also discloses an internal realignment on January 12, 2026, after which certain subsidiaries are expected to report beneficial ownership separately.
Vistagen Therapeutics, Inc. filed a current report to let investors know it has begun using a new corporate presentation as of January 9, 2026. The presentation is attached as Exhibit 99.1 and is described as the company’s corporate presentation dated January 2026.
The company notes that the information in this presentation is being furnished, not filed, which means it is not subject to certain liability provisions of the Securities Exchange Act and is not automatically incorporated into other SEC filings unless specifically referenced. No financial results, major transactions, or other operational changes are described in this report; the focus is on making the updated investor presentation publicly available.
Vistagen Therapeutics reported Q2 FY2026 results for the quarter ended September 30, 2025. Revenue was $258 thousand, while operating expenses rose to $20.3 million, driven by higher R&D ($15.9 million) and steady G&A ($4.4 million). The company posted a net loss of $19.4 million (basic and diluted net loss per share of $0.54).
Liquidity remained solid with cash, cash equivalents and marketable securities of $77.2 million as of September 30, 2025. Management concluded that “substantial doubt” exists about the company’s ability to continue as a going concern beyond twelve months from the financial statement issuance date.
Vistagen strengthened its balance sheet via its at-the-market program, selling 9,608,772 shares in the quarter for net proceeds of $27.9 million. Shares issued were 38,895,568 at September 30, 2025; as of November 12, 2025, 39,495,451 shares were outstanding. Deferred revenue totaled $2.5 million, primarily related to its AffaMed collaboration and Fuji Pharma negotiation agreement.
Vistagen Therapeutics, Inc. reported that it released its financial results for its fiscal year 2026 second quarter, which ended on September 30, 2025. The company disclosed that these results were announced in a press release dated November 13, 2025, which is included with this report as Exhibit 99.1.
The report explains that the press release and related information are being furnished, not filed, meaning they are not automatically subject to certain Exchange Act liabilities or incorporated into other securities filings unless specifically referenced.
Vistagen Therapeutics (VTGN) reported a routine insider transaction. Director Paul R. Edick acquired 35,200 stock options on 10/27/2025 at an exercise price of $3.9 per share. The options were granted in connection with his appointment to the Board and were issued under the company’s Amended and Restated 2019 Omnibus Equity Incentive Plan.
The options vest in three equal annual installments beginning on the first anniversary of the grant date and expire on 10/27/2035. Following the transaction, 35,200 derivative securities were beneficially owned directly.
Vistagen Therapeutics (VTGN) filed a Form 3 initial statement of beneficial ownership. The reporting person is identified as a Director, with the event date of 10/27/2025.
The filing states that no securities are beneficially owned as of the event date. The form was filed by one reporting person and signed by Paul R. Edick.
Vistagen Therapeutics (VTGN) furnished a Regulation FD update announcing that the last patient has completed the randomized, double-blind, placebo-controlled public speaking challenge portion of its PALISADE-3 Phase 3 clinical trial evaluating fasedienol for the acute treatment of social anxiety disorder.
The company attached a press release as Exhibit 99.1. The information was furnished under Item 7.01 and is not deemed filed under Section 18 of the Exchange Act.