VSF-173 Study in Healthy Adult Volunteers for Treatment of Induced Excessive Sleepiness

NCT00467441 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2007-11-02

No results posted yet for this study

Summary

The purpose of this study is to determine the safety and efficacy of VSF-173 compared to placebo in treatment of induced excessive sleepiness.

Conditions

  • Excessive Somnolence

Interventions

DRUG

VSF-173

Sponsors & Collaborators

Principal Investigators

  • Gunther Birznieks · Vanda Pharmaceuticals

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Countries

  • France

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00467441 on ClinicalTrials.gov