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Sponsored by: |
Egalet a/s |
Information provided by: | Egalet a/s |
ClinicalTrials.gov Identifier: | NCT00444834 |
The purpose of this study is to compare the efficacy of the Egalet® controlled release formulation to an immediate release Carvedilol tablet.
Condition | Intervention | Phase |
Hypertension |
Drug: Carvedilol |
Phase II |
MedlinePlus related topics: | Exercise and Physical Fitness High Blood Pressure |
Drug Information available for: | Carvedilol |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Active Control, Crossover Assignment, Pharmacodynamics Study |
Official Title: | A Phase II, Multi-Center, Multiple-Dose, Double-Blind, Randomized, Crossover Study Comparing the Pharmacodynamic Effects of a Once-Daily Controlled-Release Carvedilol (CRC; Egalet® Formulation) and an Immediate-Release Carvedilol (IRC) Formulation in Patients With Primary Hypertension |
Estimated Enrollment: | 40 |
Study Start Date: | April 2007 |
Estimated Study Completion Date: | October 2007 |
Estimated Primary Completion Date: | October 2007 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
1: Experimental
Egalet carvedilol
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Drug: Carvedilol
50 mg
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2: Active Comparator
Coreg
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Drug: Carvedilol
50 mg
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Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Responsible Party: | Egalet a/s ( Egalet a/s ) |
Study ID Numbers: | CL-EG-006, EudraCT no.: 2006-006534-17 |
First Received: | March 7, 2007 |
Last Updated: | February 12, 2008 |
ClinicalTrials.gov Identifier: | NCT00444834 |
Health Authority: | Denmark: Danish Medicines Agency |
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