drugset / Trial / NCT02283840

Single Dose Crossover Comparative Bioavailability Study of Eslicarbazepine Acetate Versus To-be-marketed Formulation

NCT02283840

Phase 1 Completed 60 enrolled Bial - Portela C S.A.
RandomizedCrossoverSingle-blindTreatment

Summary

Single center, randomized, single dose, laboratory-blinded, 2-period, 2-sequence, crossover design

Timeline

Start
2007-05
Primary completion
2007-06
Completion
2007-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Eslicarbazepine acetate Unknown 400 mg Oral
Subject Eslicarbazepine acetate Unknown 600 mg Oral
Subject Eslicarbazepine acetate Unknown 800 mg Oral

Indications