Trials / Completed
CompletedNCT00894088
Bioequivalency Study of Mycophenolate Mofetil 500 mg Tablets Under Fasted Conditions
A Single Dose, 2-Period, 2-Treatment 2-Way Crossover Bioequivalency Study of Mycophenolate Mofetil 500 mg Tablets Under Fasting Conditions
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 38 (actual)
- Sponsor
- Roxane Laboratories · Industry
- Sex
- All
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
The objective of this study was to prove the bioequivalence of Mycophenolate Mofetil 500 mg tablets under fasted conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Mycophenolate Mofetil | Mycophenolate Mofetil 500 mg Tablet |
Timeline
- Start date
- 2006-01-01
- Primary completion
- 2006-01-01
- Completion
- 2006-01-01
- First posted
- 2009-05-06
- Last updated
- 2018-01-23
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00894088. Inclusion in this directory is not an endorsement.