Effects of Altered Formulation on the Bioequivalence of Tacrolimus in Healthy Female and Male Adult Volunteers
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- STATUS
- Not Recruiting
Updated on 19 February 2024
Summary
The purpose of this study is to see how well the body absorbs tacrolimus after oral administration.
Description
The purpose of this study is to conduct a randomized, single dose, four-treatment, four-period cross-over in vivo bioequivalence study in 24 healthy normal adult volunteers to evaluate the in vivo performance of fresh and aged brand name and generic amorphous solid dispersion preparations.
Details
| Condition | healthy |
|---|---|
| Age | 18years - 49years |
| Clinical Study Identifier | TX5145 |
| Last Modified on | 19 February 2024 |
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