Trials / Completed
CompletedNCT01161940
Bioequivalence Study of Nizatidine Capsules 300 mg of Dr.Reddy's Laboratories Limited Under Fasting Conditions
A Two-way Crossover Experimental Evaluation of Relative Bioavailabilities of Two Formulations of Nizatidine 300 mg Capsules in Healthy Human Subjects Under Fasting Conditions
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 26 (actual)
- Sponsor
- Dr. Reddy's Laboratories Limited · Industry
- Sex
- Male
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
This is a bioequivalence study of nizatidine Capsules 300 mg of Dr.Reddy's Laboratories Limited under fasting conditions
Detailed description
Open label, balanced, randomized, two-treatment, two-period, two sequence, single dose, crossover, comparative oral bioavailability study in healthy, adult, male human subjects under fasting conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Nizatidine | Nizatidine Capsules 300 mg of Dr.Reddy's Laboratories Limited |
| DRUG | Axid | Axid 300 mg Capsules of Reliant Pharmaceuticals, US |
Timeline
- Start date
- 2004-07-01
- Primary completion
- 2004-09-01
- Completion
- 2004-09-01
- First posted
- 2010-07-14
- Last updated
- 2010-07-14
Source: ClinicalTrials.gov record NCT01161940. Inclusion in this directory is not an endorsement.