Open-Label Extension (OLE) Study for Safety and Efficacy of Velneperit (S-2367) in Obese Subjects
NCT00788528 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 766
Last updated 2018-05-01
Summary
The purpose of this open-label extension study is to evaluate the safety and efficacy of velneperit (S-2367) in obese subjects.
Conditions
Interventions
- DRUG
-
S-2367 (velneperit)
Tablet, 4 x 400 mg, taken once daily with morning meal, 54-weeks
Sponsors & Collaborators
-
Shionogi
lead INDUSTRY
Principal Investigators
-
Shionogi Clinical Trials Administrator Clinical Support Help Line · Shionogi
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2008-08-31
- Primary Completion
- 2010-02-28
- Completion
- 2010-03-31
Countries
- United States
Study Locations
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