Fasedienol Nasal Spray for the Acute Treatment of Anxiety in Adults With Social Anxiety Disorder (PALISADE-3)

Running, not enrolling · Phase 3 · Has a placebo group

Conditions studied: Social Anxiety Disorder

In brief

This U.S. Phase 3 clinical trial is designed to evaluate the efficacy, safety, and tolerability of the acute intranasal (i.n.) administration of Fasedienol Nasal Spray (fasedienol) (3.2 µg) to relieve symptoms of acute anxiety in adult subjects ages 18 through 65 with Social Anxiety Disorder induced by a public speaking challenge (PSC) in a clinical setting. In addition, safety and tolerability of i.n. administration of 3.2 µg of fasedienol, as-needed, up to 6 times per day for up to 12 months, will be assessed in those subjects who complete PALISADE-3 and choose to enter the distinct open-label extension phase of the study.

Key facts

Study ID

NCT06358651

Run by

VistaGen Therapeutics, Inc.

People needed

238

Starts

2024-03-28

Expected to finish

2026-10-01

Last updated by the study team

2025-11-26

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Written informed consent provided prior to conducting any study specific assessment.
• Male and female adults, 18 through 65 years of age, inclusive.
• Current diagnosis of SAD as defined in the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5), and confirmed by the Mini-International Neuropsychiatric Interview (MINI).
• Clinician-rated Liebowitz Social Anxiety Scale (LSAS) total score ≥70 at Screening (Visit 1).
• Clinician-rated Hamilton Depression Rating Scale (HAM-D) (17-items) total score <16.
• Female subjects of childbearing potential must be able to commit to the consistent and correct use of an effective method of birth control throughout the study
• Subjects must have normal olfactory function

You may not qualify if…

• Any history of bipolar disorder (I or II), schizophrenia, schizoaffective disorder, psychosis, anorexia or bulimia, premenstrual dysphoric disorder, autism spectrum disorder, or obsessive-compulsive disorder.
• Any other current principal or personality disorder (previously known as Axis I or Axis II disorders), except for specific phobias or generalized anxiety disorder, provided that these are not the primary diagnosis.
• Subjects who meet criteria for moderate or severe alcohol use disorder within the 1 year prior to study entry, or any use of illicit substances or tetrahydrocannabinol ("THC") within 2 months prior to study entry.
• In the opinion of the investigator, the subject has a significant risk for suicidal behavior during the course of their participation in the study, or the subject is considered to be an imminent danger to themself or others.
• Clinically significant nasal pathology or history of significant nasal trauma, nasal surgery, total anosmia, or nasal septum perforation that may have damaged the nasal chemosensory epithelium.
• Two or more documented failed adequate treatment trials with a registered medication approved for SAD.
• Currently receiving cognitive-behavioral therapy (CBT), exposure therapy, or acceptance and commitment therapy.
• Subjects taking psychotropic medications within 30 days before Visit 2
• Use of any over-the-counter product, prescription product, off-label treatment, cannabidiol ("CBD"), or herbal preparation for treatment of the symptoms of anxiety or social anxiety within 30 days before Visit 2.
• Prior participation in a clinical trial involving fasedienol.
• Participation in any other clinical trial within the last 30 days or during the course of the current trial.
• Subjects with a positive urine drug screen.
• Women who have a positive urine pregnancy test.
• Women who are currently breastfeeding are not eligible unless they are willing to stop breastfeeding for the duration of the study.
• Subjects who have tested positive and/or have exhibited symptoms consistent with SARS-CoV-2 infection during the 4 weeks prior to Screening (Visit 1).
• Any clinically significant medical history or findings as determined by the Investigator that could interfere with the objectives of the study or put the participant at risk.

Where it is running

• Vistagen Clinical Site — Phoenix, Arizona, United States
• Vistagen Clinical Site — Fayetteville, Arkansas, United States
• Vistagen Clinical Site — Little Rock, Arkansas, United States
• Vistagen Clinical Site — Lafayette, California, United States
• Vistagen Clinical Site — Oceanside, California, United States
• Vistagen Clinical Site — Sherman Oaks, California, United States
• Vistagen Clinical Site — Denver, Colorado, United States
• Vistagen Clinical Site — Cromwell, Connecticut, United States
• Vistagen Clinical Site — Jacksonville, Florida, United States
• Vistagen Clinical Site — Lakeland, Florida, United States
• Vistagen Clinical Site — Orlando, Florida, United States
• Vistagen Clinical Site — West Palm Beach, Florida, United States
• Vistagen Clinical Site — Chicago, Illinois, United States
• Vistagen Clinical Site — Overland Park, Kansas, United States
• Vistagen Clinical Site — Baltimore, Maryland, United States
• Vistagen Clinical Site — Boston, Massachusetts, United States
• Vistagen Clinical Site — Saint Charles, Missouri, United States
• Vistagen Clinical Site — Las Vegas, Nevada, United States
• Vistagen Clinical Site — New York, New York, United States
• Vistagen Clinical Site — Media, Pennsylvania, United States
• Vistagen Clinical Site — Memphis, Tennessee, United States
• Vistagen Clinical Site — Fort Worth, Texas, United States
• Vistagen Clinical Site — Draper, Utah, United States
• Vistagen Clinical Site — Everett, Washington, United States

Full record on ClinicalTrials.gov

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