Clinical Trials Directory

Trials / Completed

CompletedNCT01630655

Bioequivalence Study of Torrent Pharmaceuticals Ltd's Felodipine Extended-Release Tablets Under Fasting Condition

An Open Label, Randomised, 2-period, 2-treatment, 2-sequence, Cross-over, Single-dose Bioequivalence Study of Felodipine Extended-Release Tablets USP 10 mg (Test, Torrent Pharmaceuticals Ltd., India) Versus Felodipine Extended-Release Tablets USP 10 mg (Reference, Mylan Pharmaceuticals Inc., USA) in Healthy Human Volunteers Under Fasting Condition

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
Sponsor
Torrent Pharmaceuticals Limited · Industry
Sex
Male
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

Objective: Primary objective of the present study was to compare the single dose bioavailability of Torrent's Felodipine Extended-Release Tablets USP 10 mg and Innovator's (Mylan Pharmaceuticals Inc., USA) Felodipine Extended-Release Tablets USP 10 mg. Dosing periods were separated by a washout period of 17 days during fasting study. Study Design: Open-Label, Randomised, two Period, two treatment, Crossover, Single-Dose Bioequivalence Study

Conditions

Interventions

TypeNameDescription
DRUGTorrent's Felodipine Extended-Release Tablets

Timeline

First posted
2012-06-28
Last updated
2012-06-28

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT01630655. Inclusion in this directory is not an endorsement.

Bioequivalence Study of Torrent Pharmaceuticals Ltd's Felodipine Extended-Release Tablets Under Fasting Condition (NCT01630655) · Clinical Trials Directory