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Safety and Efficacy of CDB-2914 for Emergency Contraception

Emergency Contraception Clinical Trial

Official title:
A Prospective, Open-Label, Single Arm, Multicenter Study to Evaluate the Efficacy, Safety and Tolerability of CDB-2914 as Emergency Contraception When Taken Between 48 Hours and 120 Hours of Unprotected Sex

Clinical Trial Summary

The purpose of this study is to assess the safety and efficacy of CDB-2914 for preventing pregnancy when taken 3 to 5 days after unprotected sexual intercourse.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00411684
Study type Interventional
Source HRA Pharma
Contact
Status Completed
Phase Phase 3
Start date November 2006
Completion date June 5, 2009
View Details
See also
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Completed NCT03614494 - Piroxicam and Levonorgestrel Co-treatment for Emergency Contraception Phase 2/Phase 3