drugset / Trial / NCT00833664

Terbinafine HCl 250 mg Tablet Formulations Under Non-Fasting Conditions

NCT00833664

Phase 1 Completed 22 enrolled Teva Pharmaceuticals USA
RandomizedCrossoverOpen-labelOther

Summary

The Purpose of this study os to evaluate the relative bioavailability of the test formulation of terbinafine tablets with an already marketed reference formulation Lamisil® (Novartis Pharmaceuticals), under post-prandial conditions in healthy, non-tobacco using male and female adult subjects.

Timeline

Start
2002-01
Primary completion
2002-01
Completion
2002-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Terbinafine Small molecule 250 mg

Indications

No indication recorded.