Obstetrics, Gynecology and Reproductive Biology Research
Luminous Study
A Phase 3, Multicenter, Open-Label, Single Arm Study MR-100A-01 in Women of Childbearing Potential to Evaluate Contraceptive Efficacy and Safety
AGE: 16 years or older
SEX AT BIRTH: Female
SEX AT BIRTH: Female
TYPE: Interventional Study
CONDITION: Contraception
CONDITION: Contraception
HEALTHY PARTICIPANTS: Yes
COMPENSATION: For time and travel
COMPENSATION: For time and travel
Learn More About This Research Study
For more information, please contact Alyssa Mason at 440-995-3811 or complete the online form below.
Study Purpose
The purpose of this study is to learn about the effectiveness of the study drug in preventing pregnancy and the safety and tolerability of wearing the patch (side effects, menstrual cycle control, and ability of the patch to stick to the skin).
Who Can Participate
Participants who are 16 years or older, sexually active with a regular menstrual cycle may be eligible for this study. To take part in the study, you must be willing and able to:
- use the study patch as your only method of birth control
- apply the study patch at home and undertake home pregnancy tests
- complete an electronic diary with details of your menstrual cycle and sexual activity
- attend regular, scheduled visits at your nearest study center
- undergo regular study-related tests and health checks.
STUDYID#
- SSU00184830