Bioequivalence Study Of Verapamil
NCT00668967 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 79
Last updated 2009-07-08
Summary
The purpose of this study is to demonstrate bioequivalence of single doses of two verapamil formulations
Conditions
- Healthy Volunteers
Interventions
- DRUG
-
verapamil
240 mg extended release tablets once daily at bedtime for 28 days
- DRUG
-
verapamil
240 mg extended release tablets once daily at bedtime for 28 days
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Pfizer CT.gov Call Center · Pfizer
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2008-02-29
- Primary Completion
- 2008-07-31
- Completion
- 2008-07-31
Countries
- United States
Study Locations
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