Overview

Bioequivalence Study of Mycophenolate Mofetil 500 mg Tablets of Dr.Reddy's Laboratories Limited Under Fasting Conditions

Status:
Completed
Trial end date:
2007-12-01
Target enrollment:
Participant gender:
Summary
To compare the bioavailability and characterise the pharmacokinetic profile of the sponsor's test formulation with respect to the reference formulation CellceptĀ® 500 mg tablets, in healthy, adult, human male subjects under fasting conditions and to assess the bioequivalence.
Phase:
Phase 1
Details
Lead Sponsor:
Dr. Reddy's Laboratories Limited
Treatments:
Mycophenolate mofetil
Mycophenolic Acid