Trials / Completed
CompletedNCT01167933
Bioequivalence Study of Simvastatin Tablets, 80 mg of Dr. Reddy's Under Fed Conditions
A Randomized, Two-treatment, Two-period, Two-sequence, Single Dose, Crossover Bioequivalence Study of Simvastatin 80 mg Tablets of Dr. Reddy's to be Compared With Zocor® 80 mg Tablets of Merck & Co. Inc., USA in Healthy Adult Subjects Under Fed Conditions
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 44 (actual)
- Sponsor
- Dr. Reddy's Laboratories Limited · Industry
- Sex
- All
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to * compare the single dose bioavailability of Simvastatin 80 mg tablets with Zocor® 80 mg tablets of MercK \& Co. Inc, USA in healthy subjects under fed conditions * monitor adverse events and to ensure the safety of subjects.
Detailed description
A randomized, two-treatment, two-period, two-sequence, single dose, crossover bioequivalence study of Simvastatin 80 mg tablets of Dr. Reddy's Laboratories Limited to be compared with Zocor® 80 mg tablets of Merck \& Co. Inc., USA in healthy, adult, human subjects under fed conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Simvastatin | Simvastatin 80 mg tablets Dr. Reddy's Laboratories Ltd |
Timeline
- Start date
- 2005-01-01
- Primary completion
- 2005-04-01
- Completion
- 2005-04-01
- First posted
- 2010-07-22
- Last updated
- 2010-08-09
Source: ClinicalTrials.gov record NCT01167933. Inclusion in this directory is not an endorsement.