Bioequivalency Study of Perindopril Erbumine 8 mg Tablet Under Fed Conditions
NCT ID: NCT01013155
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
48 participants
INTERVENTIONAL
2007-05-31
2007-05-31
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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perindopril erbumine
8 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 Perindopril 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.
Locations
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Novum Pharmaceutical Research Services
Houston, Texas, United States
Countries
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Other Identifiers
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PERI-T8-PVFD-1
Identifier Type: -
Identifier Source: org_study_id
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