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You can access this
clinical trial
if you have
and you are
over 18
years old
This is an early phase trial to determine
the dosage and safety of the new treatment.
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The purpose

The objective of this study was to compare the oral bioavailability of an investigational formulation of mycophenolate mofetil (MMF) 250 mg capsules to an equivalent dose of the commercially available reference product, CellCept® (mycophenolate mofetil) 250 mg administered to healthy subjects following an overnight fast of at least 10 hours.

Provided treatments

  • Drug: Mycophenolate Mofetil
  • Drug: CellCept®
Tris trial is registered with FDA with number: NCT00911274. The sponsor of the trial is Teva Pharmaceuticals USA and it is looking for 53 volunteers for the current phase.
Official trial title:
A Single-Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalence Study of Mycophenolate Mofetil 250 mg Capsules Under Fasting Conditions