Study to Evaluate LevoCept, a Long-Acting Reversible Intrauterine

Build status - In Progress

Recruiting

99 years or below

All

Phase 3

1525 participants needed

1 Location

Brief description of study

The primary objective of the study is to assess the contraceptive efficacy (prevention of pregnancy) of LevoCept. The secondary objectives of the study are to assess the following for LevoCept: Safety and tolerability; Return to fertility after LevoCept removal, only for subjects requesting LevoCept removal to become pregnant; Release rate of LNG from the intrauterine system (IUS) and resulting pharmacokinetics of LNG (PK substudy only).

Detailed description of study

Eligibility of study

You may be eligible for this study if you meet the following criteria:

Conditions: Contraceptive, intrauterine device (IUD), birth control
Age: 99 years or below
Gender: All

Woman Age 18+ of child bearing age and interested in using an intrauterine device (IUD) for birth control for up to 5 years.

Updated on 04 Aug 2024. Study ID: 844951

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