Drug intelligence / Profile preview

ulipristal acetate

Development stage
Approved
Lead developer
Esteve
Modality
Small Molecules
Administration
Vaginal
01

Overview

Ulipristal acetate (UPA) is a selective progesterone receptor modulator (SPRM) being developed by the Population Council, in partnership with the National Institute of Child Health and Human Development (NICHD) and HRA Pharma, as a long-acting contraceptive vaginal ring (CVR). This matrix-type ring is designed for continuous use over a three-month period, providing a sustained release of UPA (1500-2500 μg/day) to suppress ovulation. Unlike the emergency contraceptive pill formulation (brand name ella), this program focuses on regular, estrogen-free contraception, offering a viable alternative for women who cannot use estrogen-containing products. Clinical development has progressed through Phase 1 and Phase 2 trials, evaluating the ring's efficacy in inhibiting ovulation both as a monotherapy and in combination with oral levonorgestrel, while also monitoring endometrial safety and bleeding patterns.

Brand names
ellaOneElla
Other names
ulipristal acetate contraceptive vaginal ringulipristal acetate vaginal ring
02

Targets

AR (Adrenergic receptors)GR (Glucocorticoid receptor)PR (Progesterone receptor)

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