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Clinical Trial Summary

This study is being conducted to evaluate the impact of DR-102, a 28-day oral contraceptive compared to a standard 28-day oral contraceptive regimen on hemostatic parameters in healthy women.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01388491
Study type Interventional
Source Teva Branded Pharmaceutical Products R&D, Inc.
Contact
Status Completed
Phase Phase 2
Start date October 31, 2011
Completion date September 30, 2012

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