Clinical Trials Directory

Trials / Completed

CompletedNCT01064115

Cetirizine Hydrochloride Tablets, 10 mg Bioequivalence Study of Dr.Reddy's Under Fed Condition

A Two Way, Open Label, Single Dose, Cross Over, Experimental Evaluation of Relative Bioavailabilities of Two Formulations of Cetirizine Hydrochloride Tablets 10 mg in Healthy Adult Human Male Subjects Under Fed Conditions.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Dr. Reddy's Laboratories Limited · Industry
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

A Two Way, Open Label, Single Dose, Cross Over, Experimental Evaluation of Relative Bioavailabilities of Two Formulations of Cetirizine Hydrochloride Tablets 10 mg of Dr. Reddys laboratories with Zyrtec 10 mg of Pfizer labs in Healthy Adult Human Male Subjects Under Fed Conditions.

Detailed description

Open Label, Balanced, Randomized, Two-Treatment, Two-Period, Two-Sequence, Single Dose, Cross Over, and Comparative Oral Bioavailability study in healthy, adult, human, male subjects under Fed Conditions.

Conditions

Interventions

TypeNameDescription
DRUGCetirizine HydrochlorideCetirizine Hydrochloride Tablets 10 mg

Timeline

Start date
2006-01-01
Primary completion
2006-01-01
Completion
2006-02-01
First posted
2010-02-08
Last updated
2010-02-08

Source: ClinicalTrials.gov record NCT01064115. Inclusion in this directory is not an endorsement.

Cetirizine Hydrochloride Tablets, 10 mg Bioequivalence Study of Dr.Reddy's Under Fed Condition (NCT01064115) · Clinical Trials Directory