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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00602303
Other study ID # TORE-01
Secondary ID
Status Completed
Phase N/A
First received January 15, 2008
Last updated January 19, 2018
Start date September 2003
Est. completion date September 2003

Study information

Verified date January 2018
Source West-Ward Pharmaceutical
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this study was the bioequivalence of a Roxane Laboratories' Torsemide Tablets, 20 mg, to Demadex® Tablets, 20 mg (Roche) under fasting conditions using a single-dose, 2-treatment, 2-period, crossover design.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date September 2003
Est. primary completion date September 2003
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Drug:
Torsemide


Locations

Country Name City State
United States Bio-Kinetic Clinical Applications, Inc. Springfield Missouri

Sponsors (1)

Lead Sponsor Collaborator
Roxane Laboratories

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bioequivalence Baseline, Two period, Seven day washout
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