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Bioequivalency Study of Mycophenolate Mofetil 500 mg Tablets Under Fed Conditions | Clinical Trials | Clareo Health

COMPLETEDNANCT00893958

Bioequivalency Study of Mycophenolate Mofetil 500 mg Tablets Under Fed Conditions

The objective of this study was to prove the bioequivalence of Mycophenolate Mofetil 500 mg tablets under fed conditions.

Lead sponsor: Roxane Laboratories•1 U.S. locations•View source on ClinicalTrials.gov

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COMPLETEDNA

Bioequivalency Study of Mycophenolate Mofetil 250 mg Capsules Under Fasted Conditions

NCT00893542 · Prophylaxis of Organ Rejection

Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: January 23, 2018Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment39

Start dateJan 2006

Last updatedJan 23, 2018

Condition

Prophylaxis of Organ Rejection

Locations shown

CEDRA Clinical Research

Austin, Texas

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 23, 2018Data synced to Clareo: May 10, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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