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
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
- lead INDUSTRY
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
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