Bioequivalency Study of Famciclovir 500 mg Tablets Under Fasted Conditions
NCT ID: NCT01321515
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
36 participants
INTERVENTIONAL
2007-07-31
2007-07-31
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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famciclovir
500 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 famciclovir, penciclovir 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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Benno G Roesch, M.D.
Role: PRINCIPAL_INVESTIGATOR
Advanced Biomedical Research
Locations
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Advanced Biomedical Research, Inc.
Hackensack, New Jersey, United States
Countries
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Other Identifiers
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FAMC-T500-PVFS-1
Identifier Type: -
Identifier Source: org_study_id
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