A Study to Assess the Pharmacologic Equivalence of Two Orlistat Dosage Forms
NCT01550926 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 48
Last updated 2013-01-28
Summary
The purpose of this study is to determine whether a new dosage form and dose of orlistat is equivalent to the currently marketed form.
Conditions
Interventions
- DRUG
-
120 mg orlistat
2 X60 mg capsule
- DRUG
-
60 mg orlistat
60 mg orlistat
- DRUG
-
orlistat experimental dose
experimental
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
GSK Clinical Trials · GlaxoSmithKline
Study Design
- Allocation
- RANDOMIZED
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2009-02-28
- Primary Completion
- 2009-03-31
- Completion
- 2009-03-31
Countries
- United Kingdom
Study Locations
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