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VistaGen Therapeutics clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our USA register with VistaGen Therapeutics as lead sponsor. Synced 26 Sep 2026
3Current trials
1Recruiting now
1Drug in these trials
1Trial register
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

VistaGen Therapeutics is the lead sponsor of 3 current clinical trials in our USA register. 1 is recruiting patients now. The most common phase is Phase 3. The drugs named most often in its trials are Fasedienol. The most-studied condition is Social Anxiety Disorder.

ClinicalTrials.gov trials by status

  • Recruiting133%
  • Active, closed267%

Trials by phase

  • Phase 3267%
  • Phase 2133%
01

Clinical trials sponsored by VistaGen Therapeutics

3 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
A Clinical Trial to Assess the Efficacy, Safety, and Tolerability of a Repeat Dose of Fasedienol Nasal Spray for the Acute Treatment of Anxiety in Adults With Social Anxiety Disorder
NCT06809179 · Social Anxiety Disorder
Phase 2 Recruiting 2025-01 USA
Fasedienol Nasal Spray for the Acute Treatment of Anxiety in Adults With Social Anxiety Disorder (PALISADE-4)
NCT06615557 · Social Anxiety Disorder (SAD)
Phase 3 Active, closed 2024-09 USA
Fasedienol Nasal Spray for the Acute Treatment of Anxiety in Adults With Social Anxiety Disorder (PALISADE-3)
NCT06358651 · Social Anxiety Disorder
Phase 3 Active, closed 2024-03 USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Drugs in VistaGen Therapeutics trials

1 compound

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

03

Conditions in VistaGen Therapeutics trials

2 conditions
Social Anxiety Disorder2Social Anxiety Disorder (SAD)1
04

By trial register

RegisterTrialsRecruiting
Clinical trials in USA31

A trial with sites in more than one country appears in each of those registers.

05

Questions about VistaGen Therapeutics trials

How many clinical trials does VistaGen Therapeutics sponsor?

VistaGen Therapeutics is the lead sponsor of 3 current trials on ClinicalTrials.gov in our USA register, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are VistaGen Therapeutics trials recruiting?

Yes. 1 of its 3 ClinicalTrials.gov trials is recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is VistaGen Therapeutics testing?

Its current trials name 1 drug or biological as interventions. The most frequent are Fasedienol (2). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.