drugset / Trial / NCT01046214

Bupropion Hydrochloride 300 mg Extended Release Tablets Under Fasting Conditions

NCT01046214 ↗

Phase 1 Terminated 8 enrolled Teva Pharmaceuticals USA
RandomizedCrossoverQuadruple-blind

Summary

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.

Timeline

Start
2010-01
Primary completion
—
Completion
—

Outcome

Outcome not reported

Stopped (Enrollment): “Recruitment issues”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bupropion Small molecule 300 mg —

Indications