To Demonstrate the Relative Bioequivalence of Lisinopril 1 x 40 mg Tablet Under Fasting and Fed
NCT ID: NCT00883506
Last Updated: 2017-03-29
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
24 participants
INTERVENTIONAL
2000-05-31
2000-06-30
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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1
Lisinopril 40 mg Tablet under fed conditions.
Lisinopril 40 mg Tablet under fed conditions.
2
Lisinopril 40 mg Tablet (Zestril)
Lisinopril 40 mg Tablet (Zestril) under fed conditions.
3
Lisinopril 40 mg Tablet under fasting conditions.
Lisinopril 40 mg Tablet under fasting conditions.
Interventions
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Lisinopril 40 mg Tablet (Zestril) under fed conditions.
Lisinopril 40 mg Tablet under fasting conditions.
Lisinopril 40 mg Tablet under fed conditions.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Treatment for drug or alcohol dependence.
18 Years
55 Years
MALE
Yes
Sponsors
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Sandoz
INDUSTRY
Responsible Party
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Sandoz Inc.
Principal Investigators
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Eric Masson, Pharm.D.
Role: PRINCIPAL_INVESTIGATOR
Anapharm
Other Identifiers
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00104
Identifier Type: -
Identifier Source: org_study_id
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