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Clinical Trial Summary

This trial will study the percentage of women with at least one occurrence of intracyclic bleeding (bleeding and/or spotting) during the cycles 2 and 3 of treatment with test or reference drug.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01557023
Study type Interventional
Source Eurofarma Laboratorios S.A.
Contact
Status Withdrawn
Phase Phase 3
Start date July 1, 2013
Completion date December 1, 2014

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