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Contraceptive Study

A Single Arm, Open-Label Pivotal Contraceptive Efficacy Study of Ovaprene®

physician talking with patient

 

AGE: 18 - 40 years old
SEX AT BIRTH: Female
HEALTHY PARTICIPANTS: Yes
TYPE: Experimental Intervention Study
CONDITION: Birth control, contraceptive
LOCATION: University Hospitals Landerbrook Medical Center

Learn More About This Research Study

Please call study coordinator, MacDonald Clinical Research Unit at 440-995-3810 or complete the form below.

Study Purpose

The purpose of this research study is to find out how well the investigational contraceptive, Ovaprene prevents pregnancy in women who can become pregnant.

Who Can Participate

Participants assigned female at birth who are 18 years and older who are sexually active may be eligible for this study.

Request More Information

To learn more about this study, please fill out the form below to request more information.

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  • StudyID# Site00002132