VEC-162 Study in Healthy Adult Volunteers in a Model of Insomnia
Public ClinicalTrials.gov record NCT00291187. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Study to Investigate the Efficacy and Safety of VEC-162 and Matching Placebo in Healthy Male and Female Subjects With Induced Transient Insomnia
Study identification
- NCT ID
- NCT00291187
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- Vanda Pharmaceuticals
- Industry
- Enrollment
- 411 participants
Conditions and interventions
Conditions
Interventions
- 20 mg VEC-162 Drug
- 50 mg VEC-162 Drug
- 100 mg VEC-162 Drug
- Placebo Drug
Drug
Eligibility (public fields only)
- Age range
- 21 Years to 50 Years
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jan 31, 2006
- Primary completion
- Jul 31, 2006
- Completion
- Jul 31, 2006
- Last update posted
- Oct 14, 2014
2006
United States locations
- U.S. sites
- 19
- U.S. states
- 12
- U.S. cities
- 19
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Vanda Investigational Site | Birmingham | Alabama | — | — |
| Vanda Investigational Site | Phoenix | Arizona | — | — |
| Vanda Investigational Site | San Diego | California | — | — |
| Vanda Investigational Site | San Francisco | California | — | — |
| Vanda Investigational Site | Santa Monica | California | — | — |
| Vanda Investigational Site | Miami | Florida | — | — |
| Vanda Investigational Site | Naples | Florida | — | — |
| Vanda Investigational Site | Pembroke Pines | Florida | — | — |
| Vanda Investigational Site | St. Petersburg | Florida | — | — |
| Vanda Investigational Site | Atlanta | Georgia | — | — |
| Vanda Investigational Site | Overland Park | Kansas | — | — |
| Vanda Investigational Site | Chevy Chase | Maryland | — | — |
| Vanda Investigational Site | New York | New York | — | — |
| Vanda Investigational Site | Rochester | New York | — | — |
| Vanda Investigational Site | Raleigh | North Carolina | — | — |
| Vanda Investigational Site | Cincinnati | Ohio | — | — |
| Vanda Investigational Site | Columbia | South Carolina | — | — |
| Vanda Investigational Site | Austin | Texas | — | — |
| Vanda Investigational Site | Plano | Texas | — | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00291187, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Oct 14, 2014 · Synced Jul 21, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00291187 live on ClinicalTrials.gov.