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Transdermal Contraceptive Delivery System (TCDS), Also Known as AG200-15 Patch Arm — ATI-CL13  

Contraception Clinical Trial

Official title:
An Open-Label, Randomized, Phase 3 Study of the Contraceptive Efficacy and Safety of Agile Transdermal Contraceptive Delivery System in Comparison to an Oral Contraceptive Containing 150 mcg LNG and 30 mcg EE

Clinical Trial Summary

The purpose of the study is to evaluate the efficacy and safety of a low dose transdermal contraceptive delivery system containing ethinyl estradiol and levonorgestrel.

Clinical Trial Description

Comparative evaluation of AG200-15 versus OC with regard to safety, contraceptive efficacy, hormone related adverse events, lipid profile, cycle control (bleeding pattern), subject compliance and serum concentrations of EE and LNG. To evaluate TCDS wearability (including adhesion). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01236768
Study type Interventional
Source Agile Therapeutics
Contact
Status Completed
Phase Phase 3
Start date October 2010
Completion date June 2011
View Details
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