drugset / Trial / NCT00650520

Fed Study of (Parlodel®) 2.5 mg Bromocriptine Mesylate Tablets

NCT00650520

Phase 1 Completed 119 enrolled Mylan Pharmaceuticals Inc
RandomizedCrossoverOpen-labelOther

Summary

The objective of this study is to assess the single-dose relative bioavailability of Mylan Pharmaceuticals Inc. and Novartis Pharmaceuticals Corporation (Parlodel®) 2.5 mg bromocriptine mesylate tablets, following the administration of a 10 mg dose, under fed conditions.

Timeline

Start
2007-05
Primary completion
2007-07
Completion
2007-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Bromocriptine Small molecule 10 mg

Indications

No indication recorded.