Bioequivalency Study of Losartan Potassium/Hydrochlorothiazide 100 mg/25 mg Tablet Under Fasted Conditions
NCT ID: NCT01102478
Last Updated: 2018-01-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2005-02-28
2005-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Interventions
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losartan potassium / hydrochlorothiazide
100 mg / 25 mg tablet
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Treatment with known enzyme altering drugs.
* History of allergic or adverse response to losartan potassium hydrochlorothiazide or any comparable or similar product.
18 Years
45 Years
ALL
Yes
Sponsors
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Roxane Laboratories
INDUSTRY
Responsible Party
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Roxane Laboratories, Inc.
Principal Investigators
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Daniel V Freeland, D.O.
Role: PRINCIPAL_INVESTIGATOR
CEDRA Clinical Research, LLC
Locations
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CEDRA Clinical Research, LLC
Austin, Texas, United States
Countries
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Other Identifiers
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LOHY-T100/25-PVFS-1
Identifier Type: -
Identifier Source: org_study_id
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