Bioequivalency Study of Torsemide Tablets Under Fed Conditions
Not Applicable
Completed
- Conditions
- Edema
- Registration Number
- NCT00602615
- Lead Sponsor
- Roxane Laboratories
- Brief Summary
The objective of this study was the bioequivalence of a Roxane Laboratories' Torsemide Tablets, 20 mg, to Demadex® Tablets, 20 mg (Roche) under fed conditions using a single-dose, 2-treatment, 2-period, crossover design.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 28
Inclusion Criteria
- No clinically significant abnormal findings on the physical examination, medical history, or clinical laboratory results during screening.
Exclusion Criteria
- Positive test for HIV, Hepatitis B, or Hepatitis C.
- Treatment with known enzyme altering drugs.
- History of allergic or adverse response to Torsemide or any comparable or similar product.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Bioequivalence Baseline, Two period, Seven day washout
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
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Are there specific biomarkers that correlate with enhanced diuretic response to torsemide in nephrotic syndrome?
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Trial Locations
- Locations (1)
Bio-Kinetic Clinical Applications, Inc.
🇺🇸Springfield, Missouri, United States
Bio-Kinetic Clinical Applications, Inc.🇺🇸Springfield, Missouri, United States