Overview

Bioequivalence Evaluation of Two Film-Coated Formulations of Valsartan 160 mg

Status:
Completed
Trial end date:
2014-03-01
Target enrollment:
Participant gender:
Summary
This was a randomized, single-blind, two-period, two sequence cross-over study under fasting condition, with a one-week wash-out period, to compare the pharmacokinetic profiles and bioavailability of two formulations (the test and reference) of valsartan 160 mg film-coated caplets.
Phase:
N/A
Details
Lead Sponsor:
Dexa Medica Group
Treatments:
Valsartan