This study will compare two different formulations of vabicaserin.
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Full eligibility criteria for NCT00928551
Ages eligible for Study
18 Years to 50 Years
Genders eligible for Study
Accepts Healthy Volunteers
Sexually active men must agree to use a medically acceptable form of contraception during the study and continue it for 12 weeks after investigational product administration.
Nonsmoker or smoker of fewer than 10 cigarettes per day as determined by history. Must be able to abstain from smoking during the inpatient stay.
Use of any investigational or prescription drug within 30 days before investigation product administration.
Consumption of any caffeine-containing products (eg, coffee, tea, chocolate, or soda) or alcoholic beverages within 48 hours before study day 1.
Use of any over-the-counter drugs, including herbal supplements within 72 hours before study day 1.
All locations for NCT00928551
United States (1)
Brighton, Massachusetts, United States, 2135
View full eligibility
Tris trial is registered with FDA with number: NCT00928551. The sponsor of the trial is Wyeth is now a wholly owned subsidiary of Pfizer and it is looking for 15 volunteers for the current phase.
Official trial title: A Randomized, Open-Label, Single-Dose, 3-Period Crossover, Comparative Study of a Modified Formulation of Vabicaserin (SCA-136) Versus the Reference Formulation in Healthy Subjects
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