Overview

Mycophenolate Mofetil Tablets Under Fasting Conditions

Status:
Completed
Trial end date:
2006-08-01
Target enrollment:
Participant gender:
Summary
The objective of this study was to evaluate the comparative bioavailability between Mycophenolate Mofetil 500 mg Tablets (test) and CellCeptĀ® 500 mg tablets (reference), after a single-dose in healthy subjects under fasting conditions.
Phase:
Phase 1
Details
Lead Sponsor:
Teva Pharmaceuticals USA
Treatments:
Mycophenolate mofetil
Mycophenolic Acid