Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 3

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

NCT07221578 · View on ClinicalTrials.gov ↗

Study Summary

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.

Interventions

  • DRUG Placebo
  • DRUG VQW-765

Study Locations (20)

California

  • Vanda Investigational Site — Encino
  • Vanda Investigational Site — Newport Beach
  • Vanda Investigational Site — San Diego
  • Vanda Investigational Site — San Jose
  • Vanda Investigational Site — Walnut Creek

Florida

  • Vanda Investigational Site — Jacksonville
  • Vanda Investigational Site — Miami
  • Vanda Investigational Site — Orlando
  • Vanda Investigational Site — Tampa

Arizona

  • Vanda Investigational Site — Phoenix
  • Vanda Investigational Site — Scottsdale

Georgia

  • Vanda Investigational Site — Atlanta
  • Vanda Investigational Site — Suwanee

Maryland

  • Vanda Investigational Site — Pikesville
  • Vanda Investigational Site — Rockville

Missouri

  • Vanda Investigational Site — Saint Charles
  • Vanda Investigational Site — St Louis

Colorado

  • Vanda Investigational Site — Denver

Louisiana

  • Vanda Investigational Site — New Orleans

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2025-09-22
Est. Completion 2027-04
Phase Phase 3

Sponsor

Vanda Pharmaceuticals

34 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07221578

The ClinicalTrials.gov registry entry for NCT07221578 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanda Pharmaceuticals, which has 34 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Social Anxiety Disorder (SAD) appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07221578 reports 20 study locations spanning 9 distinct geographic areas — top geographies include California, Florida, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07221578 about?

NCT07221578 is a clinical study titled "Study to Evaluate the Efficacy and Safety of VQW-765 for the On-Demand Treatment of Social Anxiety Disorder". 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.

What is the current status of trial NCT07221578?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 500 participants. The study started on 2025-09-22. Estimated completion is 2027-04.

What conditions does trial NCT07221578 study?

This clinical trial studies the following conditions: Social Anxiety Disorder (SAD). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07221578?

The interventions under investigation include: Placebo (DRUG), VQW-765 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07221578?

This trial is sponsored by Vanda Pharmaceuticals, which has 34 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07221578 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial