Philadelphia, Pennsylvania, 19148, United States
NCT Number: NCT00541996
Study Comparing Bioavailability of Oral Formulations of Vabicaserin
The purpose of this study is to determine the absorption rate of four oral formulations of vabicaserin.
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Notify MeKey information
Age range
18 year–50 year
Sex eligibility
Male
Study type
Interventional
Phase
Phase 1
Primary location
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Healthy men aged 18-50 years.
Exclusion criteria
- Any significant disease state.
- History of drug or alcohol abuse within 1 year.
- Abnormal liver function tests.
Treatment and study plan
vabicaserin
DrugPrimary outcomes
-
Assess the bioavailability of four oral formulations of vabicaserin.
Secondary outcomes
-
Obtain additional safety and tolerability data for vabicaserin in healthy male subjects.
Sponsors and collaborators
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Registry information
Official study title
A Randomized, Open-Label, Single-Dose, 4-Period Crossover, Comparative Bioavailability Study of 3 Sustained- Release Formulations and an Immediate- Release Formulation of Vabicaserin (SCA-136) in Healthy Subjects
Important dates
- Study start
- 2007
- Study completion
- 2007
- First posted
- Oct 10, 2007
- Registry last updated
- Dec 5, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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