Contraception Clinical Trial
Official title:
A Multi-center, Randomized Study of the Efficacy of Ulipristal Acetate (UPA) 30 mg, Levonorgestrel (LNG) 1.5 mg, and LNG 3.0 mg for Emergency Contraception (EC) in Women With Weight ≥ 80 kg
The proposed research study is a Phase IIb, multi-center, single-blind, randomized study of UPA 30 mg, LNG 1.5 mg and LNG 3.0 mg to evaluate EC effectiveness in women with weight ≥ 80 kg who present within 72 hours of unprotected intercourse.
Orally-dosed emergency contraception (EC) is highly effective when used properly. EC is up to
90% effective at preventing pregnancy following unprotected intercourse. Both ulipristal
acetate (UPA) and levonorgestrel (LNG) delay or inhibit ovulation when used for EC. For
individual women, use of EC provides a critical backup to prevent unintended pregnancy.
However, obesity may severely impair EC effectiveness. Data from two large randomized control
trials to identify risk factors for EC failure. A woman of obese body mass index (BMI)
(≥30mg/kg2) using LNG-based EC had more than a 4 times greater risk of pregnancy compared to
her normal BMI counterpart and a woman of overweight BMI (25-29.9) was at twice the risk of
pregnancy. Failure was also associated with a high body weight. LNG-based EC appears to have
a ceiling of efficacy at 70 kg and no efficacy for women 80 kg and above. It is believed that
by doubling the dose to LNG 3.0 mg, serum levels of LNG are corrected to a therapeutic range.
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