Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

VEC-162 Study in Adult Patients With Primary Insomnia

ClinicalTrials.gov ID: NCT00548340

Public ClinicalTrials.gov record NCT00548340. 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.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 10:20 AM EDT

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 (20 mg/Day and 50 mg/Day) in the Treatment of Primary Insomnia

Study identification

NCT ID
NCT00548340
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Vanda Pharmaceuticals
Industry
Enrollment
322 participants

Conditions and interventions

Interventions

  • VEC-162 20 mg Drug
  • Placebo Drug
  • VEC-162 50 mg Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 64 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2007
Primary completion
Jan 31, 2008
Completion
May 31, 2008
Last update posted
Oct 14, 2014

2007 – 2008

United States locations

U.S. sites
35
U.S. states
20
U.S. cities
35
Facility City State ZIP Site status
Vanda Investigational Site Birmingham Alabama
Vanda Investigational Site Hot Springs Arkansas
Vanda Investigational Site Little Rock Arkansas
Vanda Investigational Site Anaheim California
Vanda Investigational Site Burbank California
Vanda Investigational Site Los Angeles California
Vanda Investigational Site San Diego California
Vanda Investigational Site Santa Monica California
Vanda Investigational Site Colorado Springs Colorado
Vanda Investigational Site Hallandale Florida
Vanda Investigational Site Miami Florida
Vanda Investigational Site Naples Florida
Vanda Investigational Site Orlando Florida
Vanda Investigational Site Pembroke Pines Florida
Vanda Investigational Site St. Petersburg Florida
Vanda Investigational Site Atlanta Georgia
Vanda Investigational Site Chicago Illinois
Vanda Investigational Site Overland Park Kansas
Vanda Investigational Site Crestview Hills Kentucky
Vanda Investigational Site Lexington Kentucky
Vanda Investigational Site Louisville Kentucky
Vanda Investigational Site Chevy Chase Maryland
Vanda Investigational Site Newton Massachusetts
Vanda Investigational Site Troy Michigan
Vanda Investigational Site Chesterfield Missouri
Vanda Investigational Site Las Vegas Nevada
Vanda Investigational Site New York New York
Vanda Investigational Site West Seneca New York
Vanda Investigational Site Raleigh North Carolina
Vanda Investigational Site Beachwood Ohio
Vanda Investigational Site Cincinnati Ohio
Vanda Investigational Site Oklahoma City Oklahoma
Vanda Investigational Site Columbia South Carolina
Vanda Investigational Site Austin Texas
Vanda Investigational Site Dallas 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 NCT00548340, 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 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00548340 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →