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
| Type | Name | Description |
|---|---|---|
| DRUG | Cetirizine Hydrochloride | Cetirizine 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.