This study is currently not recruiting participants.
Effects of Altered Formulation on the Bioequivalence of Tacrolimus in Healthy Female and Male Adult Volunteers
Not Recruiting
18 years - 49 years
All
Phase
N/A
Brief description of study.
The purpose of this study is to see how well the body absorbs tacrolimus after oral administration.
Detailed description of study
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.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
Conditions:healthy
Age:
18 years - 49 years
Gender: All
Updated on
20 May 2015.
Study ID: 1409250017
Interested in the study?
Select a study center that’s convenient for you, and get in touch with the study team.
