Bioequivalence Study of Minocycline 100mg Tablets Under Fasting Conditions
Status:
Completed
Trial end date:
2003-01-01
Target enrollment:
Participant gender:
Summary
The purpose of this study was to determine the bioequivalence of Minocycline formulations
after administration of single doses to normal healthy subjects under fasted conditions.
These data were to be evaluated statistically to determine if the products meet
bioequivalence criteria.