Overview

Minocycline Bioequivalence Study

Status:
Completed
Trial end date:
2013-06-01
Target enrollment:
Participant gender:
Summary
This study compared the bioavailability of two formulations 100 mg (one capsule or other respectively) of each one of the products, of Minocycline, under fasting conditions, in healthy Mexican volunteers of both sexes. The single dose study under fasting (10 hours prior to study) conditions, cross, with two treatments, two periods, two sequences (2x2) randomized sequence, balanced, and with a washout period of at least 7 days between each dose, in 24 healthy volunteers.
Phase:
Phase 1
Details
Lead Sponsor:
GlaxoSmithKline
Collaborator:
CECYC (Center of Scientific and Clinical Studies, CRO)
Treatments:
Minocycline