drugset / Trial / NCT01388491

A Multinational Study to Evaluate the Effects of a 28-Day Oral Contraceptive on Hemostatic Parameters in Healthy Women

NCT01388491

Phase 2 Completed 293 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedParallel-groupOpen-labelBasic science

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.

Timeline

Start
2011-10-31
Primary completion
2012-09-30
Completion
2012-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ethinyl estradiol Small molecule 20 ug Oral
Background Desogestrel Small molecule 150 ug Oral