Efficacy and Safety of Two Flexible Extended Regimens of BAY86-5300 (SH T00186D) in Comparison With the Conventional Regimen of YAZ

Completed · Phase 3

Conditions studied: Contraception, Ovulation Inhibition, Contraceptives, Oral

In brief

The purpose of this study is to determine whether the study drug is safe and effective.

Key facts

Study ID

NCT00567164

Run by

Bayer

People needed

1887

Starts

2007-10-01

Expected to finish

2009-11-01

Last updated by the study team

2014-03-12

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Healthy women between 18 and 45 requesting oral contraception. Smokers may not exceed 35 years of age.

You may not qualify if…

• The use of steroidal oral contraceptives, or any drug that could alter oral contraception metabolism will be prohibited during the study.

Where it is running

• Study site — Chandler, Arizona, United States
• Study site — Mesa, Arizona, United States
• Study site — Mesa, Arizona, United States
• Study site — Phoenix, Arizona, United States
• Study site — Tempe, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Anaheim, California, United States
• Study site — Beverly Hills, California, United States
• Study site — Pacific Palisades, California, United States
• Study site — San Diego, California, United States
• Study site — San Diego, California, United States
• Study site — Santa Ana, California, United States
• Study site — Vallejo, California, United States
• Study site — Colorado Springs, Colorado, United States
• Study site — Denver, Colorado, United States
• Study site — Greenwood Village, Colorado, United States
• Study site — Littleton, Colorado, United States
• Study site — Waterbury, Connecticut, United States
• Study site — Boynton Beach, Florida, United States
• Study site — Brooksville, Florida, United States
• Study site — Clearwater, Florida, United States
• Study site — Coral Gables, Florida, United States
• Study site — Crystal River, Florida, United States
• Study site — Montgomery, Alabama, United States

Full record on ClinicalTrials.gov

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