Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Proellex-V is a proprietary vaginal suppository formulation of telapristone acetate, a synthetic, steroidal selective progesterone receptor modulator (SPRM) that functions as an anti-progestin by antagonizing the progesterone receptor in progesterone-sensitive tissues. Developed by Repros Therapeutics as a local vaginal delivery alternative to oral Proellex, it was investigated primarily for the treatment of symptomatic uterine fibroids, with the goal of reducing excessive menstrual bleeding and fibroid-related symptoms while maintaining systemic estrogen levels and thereby preserving bone mineral density. By opposing progesterone’s proliferative and survival signals in uterine and fibroid tissue, Proellex-V is intended to shrink progesterone-sensitive tumors and improve quality-of-life measures such as bleeding scores and symptom severity, with vaginal delivery designed to optimize systemic exposure and mitigate liver toxicity observed with higher-dose oral telapristone.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Proellex-V.