drugset / Trial / NCT02817828

E4 FREEDOM (Female Response Concerning Efficacy and Safety of Estetrol/Drospirenone as Oral Contraceptive in a Multicentric Study) - EU/Russia Study

NCT02817828

Phase 3 Completed 1577 enrolled Estetra PRA Health Sciences · collab
NaSingle-groupOpen-labelPrevention

Summary

The objectives of this study are to evaluate the contraceptive efficacy, vaginal bleeding pattern (cycle control), and the general safety and acceptability of the 15 mg estetrol (E4)/3 mg drospirenone (DRSP) combination in healthy women aged 18 to 50 years.

Timeline

Start
2016-06
Primary completion
2018-04-26
Completion
2018-04-26

Drugs

EvaluationDrugModalityDoseRoute
Subject ESTETROL ANHYDROUS Other / unclassified 15 mg Oral
Subject drospirenone Unknown 3 mg Oral

Indications

No indication recorded.