A Relative Bioavailability Study of Moexipril HCl 15 mg Tablets Under Fasting Conditions
NCT ID: NCT00992862
Last Updated: 2013-09-26
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
PHASE1
60 participants
INTERVENTIONAL
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
Study Groups
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Moexipril HCl 15mg Tablets
Moexipril HCl 15mg Tablets, Paddock Laboratories, Inc.
Univasc® 15mg Tablets
Univasc® 15mg Tablets
Interventions
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Moexipril HCl 15mg Tablets, Paddock Laboratories, Inc.
Univasc® 15mg Tablets
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* History of allergy or sensitivity to Moexipril HCl or related drugs
18 Years
45 Years
ALL
Yes
Sponsors
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Paddock Laboratories, Inc.
INDUSTRY
Principal Investigators
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Kennedy, M.D.
Role: PRINCIPAL_INVESTIGATOR
Novum Pharmaceutical Research Services
Locations
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Novum Pharmaceutical Research Services
Pittsburgh, Pennsylvania, United States
Countries
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Other Identifiers
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B035302
Identifier Type: -
Identifier Source: org_study_id