Bioequivalency Study of Mycophenolate Mofetil 500 mg Tablets Under Fed Conditions

Completed · Not applicable

Conditions studied: Prophylaxis of Organ Rejection

In brief

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

Key facts

Study ID

NCT00893958

Run by

Roxane Laboratories

People needed

39

Starts

2006-01-01

Expected to finish

2006-01-01

Last updated by the study team

2018-01-23

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• No clinically significant abnormal findings on the physical examination, medical history, or clinical laboratory results during screening

You may not qualify if…

• Positive test for HIV, Hepatitis B, or Hepatitis C. Treatment with known enzyme altering drugs. History of allergic or adverse response to mycophenolate mofetil or any comparable or similar product.

Where it is running

• CEDRA Clinical Research — Austin, Texas, United States

Full record on ClinicalTrials.gov

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