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Study identifier: NCT07221578 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Active Not Recruiting

Study to Evaluate the Efficacy and Safety of VQW-765 for the On-Demand Treatment of Social Anxiety Disorder

Condition: Social Anxiety Disorder (SAD)  ·  Sponsor: Vanda Pharmaceuticals

PhasePhase 3
Planned participants500
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNoCheck eligibility criteria ↓
Where30 locations

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

This is a multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of a single oral dose of VQW-765 compared to placebo in adults with social anxiety disorder.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: 1. Ability and willingness to provide written informed consent. 2. Male and female subjects aged 18-65 years, inclusive. 3. Current diagnosis of social anxiety disorder. 4. Liebowitz Social Anxiety Scale total score ≥60. 5. Public Speaking Anxiety Scale total score ≥60. 6. Hamilton Depression Rating Scale score ≤18. Exclusion Criteria: 1. Suicide attempts and/or suicidal ideation in the past 2 years or currently at risk of suicide in the opinion of the investigator. 2. History of bipolar disorder, schizophrenia, psychosis, seizures, delusional disorders, obsessive-compulsive disorder, or autism spectrum disorder. 3. Posttraumatic stress disorder or an eating disorder in the past 6 months. 4. Substance or alcohol use disorder in the past 6 months or positive in drug/alcohol screening. 5. Psychotherapy in the past 6 months. 6. Psychotropic medication in the past 2 months. 7. Current or planned pregnancy or nursing during the trial period. 8. Any other reason as determined by the Investigator which may lead to an unfavorable risk-benefit of study participation, or interference with study objectives.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (30)

Vanda Investigational SitePhoenix, Arizona, United States
Vanda Investigational SiteScottsdale, Arizona, United States
Vanda Investigational SiteEncino, California, United States
Vanda Investigational SiteMission Viejo, California, United States
Vanda Investigational SiteSan Diego, California, United States
Vanda Investigational SiteSan Jose, California, United States
Vanda Investigational SiteWalnut Creek, California, United States
Vanda Investigational SiteDenver, Colorado, United States
Vanda Investigational SiteJacksonville, Florida, United States
Vanda Investigational SiteMiami, Florida, United States
Vanda Investigational SiteOrlando, Florida, United States
Vanda Investigational SiteTampa, Florida, United States

+ 18 more locations — full list on the registry record.

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