VTGNNasdaqPharmaceutical PreparationsUS GAAP · USD

Vistagen Therapeutics, Inc.

Vistagen Therapeutics is a U.S.-based clinical-stage biopharmaceutical company focused on neuroscience disorders. Its pipeline centers on pherine product candidates, including intranasal therapies being developed for anxiety, depression, and other central nervous system indications.

Revenue1.3m USD
+161.1 %y/y
Operating profit (EBIT)-72.1m USD
−28.9 %y/y
EBIT margin-5,683.7%
+5,833.4 ppy/y
Net income-69.7m USD
−35.5 %y/y

Fiscal year 2026 · change from previous year

Development 2021–2026

-80-60-40-20020m USD2021: 1.1 m USD2021: EBIT -18 m USD20212022: 1.1 m USD2022: EBIT -48 m USD20222023: -0.23 m USD2023: EBIT -59 m USD20232024: 1.1 m USD2024: EBIT -33 m USD20242025: 0.49 m USD2025: EBIT -56 m USD20252026: 1.3 m USD2026: EBIT -72 m USD20261.3-72
RevenueOperating profit (EBIT)

Business

Share of revenue
Pherine product candidates95 %

Intranasal neuroscience drug candidates designed to treat anxiety, mood, and related disorders.

Sublicense and other revenue5 %

Revenue recognized from collaboration, sublicense, and related contractual arrangements.

Customers

Vistagen does not yet sell approved commercial products; its economic counterparties are primarily licensing partners, research collaborators, CROs, CDMOs, and clinical trial sites. If approved, its end customers would be patients treated by physicians in psychiatry, neurology, women’s health, and other specialty care settings.

Licensing and collaboration partners

Buy or license development rights and support commercialization through strategic agreements.

CROs and CDMOs

Provide outsourced development, testing, and manufacturing capacity that enables the pipeline.

Clinical trial sites and investigators

Run the studies needed to generate safety and efficacy data for regulatory approval.

Specialty physicians and patients

Future end users of approved therapies for social anxiety, depression, and related disorders.

Strategy

The company’s strategy is to advance its lead pherine candidates through clinical development and regulatory review, with fasedienol as the most advanced program. It also seeks partnerships and non-dilutive funding where possible while building the manufacturing and supply chain capabilities needed for eventual commercialization.

Advance fasedienol toward approvalShort term

It is the lead asset and the most direct path to a first commercial product.

Broaden the pipeline beyond fasedienolMedium term

A broader portfolio reduces dependence on a single indication and expands future market opportunities.

Secure development and commercial supplyMedium term

Clinical and future commercial execution depend on reliable manufacturing and backup sourcing.

Geography

Vistagen is headquartered in the United States and operates from South San Francisco, California. Its development and manufacturing network is U.S.-centered, but the company also contemplates backup manufacturing and future supply arrangements outside the U.S. for approved products.

Risks

Vistagen is exposed to the typical risks of clinical-stage drug development: trial failure, regulatory delay, manufacturing complexity, and competition from larger pharmaceutical companies. Because it has not yet commercialized a product, its business depends heavily on successful clinical outcomes, access to capital, and protection of its intellectual property.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development failure1Regulatory approval risk2Funding risk3Competitive intensity4Manufacturing and supply chain execution5
Impact is the risk’s severity and likelihood how probable it is over the next few years, both assessed from the company’s reports. Numbers match the list.
  1. Clinical development failureImpact: CriticalLikelihood: Medium

    Product candidates may not demonstrate sufficient efficacy or tolerability in trials.

    ExposureFasedienolItruvonePH80Other pipeline assets
  2. Regulatory approval riskImpact: HighLikelihood: Medium

    FDA or other regulators may require additional data or reject applications.

    Exposure: Late-stage neuroscience programs

  3. Funding riskImpact: HighLikelihood: Medium

    The company expects existing resources to be insufficient beyond the near term.

    Exposure: Ongoing R&D and pre-commercial activities

  4. Competitive intensityImpact: HighLikelihood: Medium

    Large pharma and biotech firms have greater resources and established commercial reach.

    ExposureAnxietyDepressionWomen’s health markets
  5. Manufacturing and supply chain executionImpact: MediumLikelihood: Medium

    Commercial supply depends on CDMOs and future backup manufacturing arrangements.

    Exposure: Future approved pherine products

Accounting

Judgemental items
Research and development accruals

Clinical and manufacturing vendors bill on timing that may differ from work performed, requiring estimates.

Impact: Can shift expenses between periods and affect reported operating loss

Sublicense and other revenue recognition

Revenue is recognized as performance obligations are satisfied under collaboration agreements.

Impact: Can create uneven quarterly revenue recognition

Lease accounting

The company leases office and laboratory space in South San Francisco.

Impact: Affects right-of-use assets, lease liabilities, and fixed commitments

Future manufacturing and purchase obligations

Commercial supply agreements with CDMOs may create contractual commitments.

Impact: Could increase future liabilities and cash requirements

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026