Trials / Completed
CompletedNCT01888328
Bioequivalence Study of Isotretinoin Capsules 40 mg Under Fed Condition
An Open Label, Randomized, Single Dose, Oral Bioequivalence Study of Isotretinoin Capsules 40 mg of Dr. Reddy's Laboratories Limited, India Comparing With That of ACCUTANE® Capsules 40 mg of Roche Laboratories Inc., Under Fed Conditions
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 26 (actual)
- Sponsor
- Dr. Reddy's Laboratories Limited · Industry
- Sex
- Male
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to determine the pharmacokinetics and bioequivalence of isotretinoin formulations after administration of single doses to normal, non-smoking,healthy males under fed conditions
Detailed description
An open label, randomized, two-treatment, single dose, oral bioequivalence study of Isotretinoin capsules 40 mg of Dr. Reddy's Laboratories Limited,under fed conditions
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Isotretinoin | Isotretinoin Capsules,40 mg |
Timeline
- Start date
- 2001-05-01
- Primary completion
- 2001-05-01
- Completion
- 2001-06-01
- First posted
- 2013-06-27
- Last updated
- 2013-06-27
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01888328. Inclusion in this directory is not an endorsement.