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A Multiple-Dose, Double Blind, Double Dummy, Comparative Bioavailability Study of Two Formulations of Bupropion Hydrochloride 300 mg Extended Release Tablets Under Fasting Conditions

NCT01046214 Phase 1 TERMINATED

The objective of this study is to evaluate the comparative bioavailability between bupropion hydrochloride 300 mg extended release tablets (Teva Pharmaceuticals USA) and Wellbutrin XL® 300 mg extended release tablets (Biovail Pharmaceuticals, Inc.) at steady-state in patients under fasting conditions.

Details

Lead sponsorTeva Pharmaceuticals USA
PhasePhase 1
StatusTERMINATED
Enrolment8
Start date2010-01

Conditions

Interventions

Primary outcomes

Countries

United States