A Study of Controlled-Release Carvedilol Compared to Immediate-Release Carvedilol in Patients With Primary Hypertension
NCT00444834 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 14
Last updated 2016-08-29
Summary
The purpose of this study is to compare the efficacy of the Egalet® controlled release formulation to an immediate release Carvedilol tablet.
Conditions
Interventions
- DRUG
-
Carvedilol
50 mg
Sponsors & Collaborators
-
Egalet Ltd
lead INDUSTRY
Principal Investigators
-
Christine Andersen, MSc Pharm · Egalet A/S
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-04-30
- Primary Completion
- 2007-05-31
- Completion
- 2007-05-31
Countries
- Denmark
Study Locations
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