Summary:
A multicenter, open-label study to evaluate the efficacy and safety of a combination oral
contraceptive regimen for the prevention of pregnancy in women
Qualified Participants Must:
Be a sexually active female
Be 18-35 years of age
Be at risk for pregnancy
If female age 36-40 years, requesting OCs for any reason (these subjects do not have to be at risk for pregnancy
data collected will be assessed for safety only)
Qualified Participants May Receive:
Study related exams, blood work, birth control, and compensation for time and travel.