Expired Study
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Lincoln, Nebraska 68502


Purpose:

The purpose of this study is to determine how VI-0521 affect speed and reaction time on specific tasks that require eye and hand coordination, compared to placebo.


Criteria:

Inclusion Criteria: - Written consents; - Adequate contraception from screening through 28 days after the last dose of study drug for female subjects; - Healthy obese or overweight subjects with BMI between 27 and 35. Exclusion Criteria: - History of glaucoma or any past or present use of medications to treat increased intraocular pressure; - Current use of any tobacco products, including cigarettes, cigars, pipes, or chewing tobacco, or use within the three months prior to screening; - History of drug abuse during the three years prior to screening; - History of alcohol abuse, or excessive alcohol consumption, or describes themselves as non-users of alcohol; - Current depression of moderate or greater severity, or any presence or history of suicidal behavior or active suicidal ideation - More than one lifetime episode of major depression; - Currently working night shifts at a job; - On average consumes greater than two cups of coffee or xanthine-containing beverages per day (>200 mg/day) within the two weeks prior to screening; - Any use of dietary, herbal, and/or fitness/body-building supplements (with the exception of vitamins) within one month prior to screening; - Aspartate aminotransferase or alanine aminotransferase >2.5 x ULN; - Serum creatinine ≥1.5 mg/dL for men or ≥1.4 mg/dL for women.


NCT ID:

NCT00806260


Primary Contact:

Study Director
Craig Peterson
VIVUS, Inc.


Backup Contact:

N/A


Location Contact:

Lincoln, Nebraska 68502
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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