Clinical Trials Directory

Trials / Completed

CompletedNCT01321502

Bioequivalency Study of Famciclovir 500 mg Tablets Under Fed Conditions

A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Famciclovir Tablets Under Fed Conditions

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
31 (actual)
Sponsor
Roxane Laboratories · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The objective of this study was to prove the bioequivalence of Famciclovir 500 mg Tablets under fed conditions.

Conditions

Interventions

TypeNameDescription
DRUGfamciclovir500 mg tablet

Timeline

Start date
2007-07-01
Primary completion
2007-07-01
Completion
2007-07-01
First posted
2011-03-23
Last updated
2018-01-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01321502. Inclusion in this directory is not an endorsement.

Bioequivalency Study of Famciclovir 500 mg Tablets Under Fed Conditions (NCT01321502) · Clinical Trials Directory