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

COMPLETED Phase 2

Evaluating the Effects of VQW-765 vs. Placebo in Performance Anxiety

NCT04800237 · 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 male and female participants with performance anxiety.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG VQW-765

Study Locations (15)

California

  • Vanda Investigational Site — Beverly Hills
  • Vanda Investigational Site — Garden Grove
  • Vanda Investigational Site — San Jose
  • Vanda Investigational Site — Torrance

Massachusetts

  • Vanda Investigational Site — Boston
  • Vanda Investigational Site — North Dartmouth

New York

  • Vanda Investigational Site — New York
  • Vanda Investigational Site — Staten Island

Arizona

  • Vanda Investigational Site — Tempe

Florida

  • Vanda Investigational Site — Orlando

Nevada

  • Vanda Investigational Site — Las Vegas

New Jersey

  • Vanda Investigational Site — Berlin

North Carolina

  • Vanda Investigational Site — Raleigh

Trial Details

FieldValue
Enrollment Target 230 participants
Start Date 2021-02-23
Est. Completion 2022-08-02
Phase Phase 2

Sponsor

Vanda Pharmaceuticals

34 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04800237

The ClinicalTrials.gov registry entry for NCT04800237 describes a study currently listed as completed. It is categorized as Phase 2, 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 230 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 Performance Anxiety 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: NCT04800237 reports 15 study locations spanning 10 distinct geographic areas — top geographies include California, Massachusetts, New York. 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 NCT04800237 about?

NCT04800237 is a clinical study titled "Evaluating the Effects of VQW-765 vs. Placebo in Performance Anxiety". 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 male and female participants with performance anxiety.

What is the current status of trial NCT04800237?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 230 participants. The study started on 2021-02-23. Estimated completion is 2022-08-02.

What conditions does trial NCT04800237 study?

This clinical trial studies the following conditions: Performance Anxiety. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04800237?

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 NCT04800237?

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 NCT04800237 being conducted?

This trial has 15 study locations across Arizona, California, Florida, Massachusetts, Nevada. 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