Discovery of Vilaprisan (BAY 1002670): A Highly Potent and Selective Progesterone Receptor Modulator Optimized for Gynecologic Therapies

Abstract: Progesterone plays an important role in the female reproductive system. However, there is also evidence that gynecologic disorders/diseases such as uterine fibroids and endometriosis are progesterone‐dependent. Steroidal and non‐steroidal selective progesterone receptor modulators (SPRMs) have shown potential for the treatment of such diseases. Steroidal SPRMs, including mifepristone and ulipristal acetate, have proven effective in clinical trials. However, several steroidal SPRMs containing a dimethylamino substituent have been associated with elevated liver enzymes in patients. An earlier drug discovery program identified lonaprisan as a highly selective SPRM that did not show drug‐related change in liver enzyme activity. Building on data obtained from that work, here we describe the research program that culminated in the discovery of a novel steroidal SPRM, vilaprisan, which combines an extremely high potency with very favorable drug metabolism and pharmacokinetic properties. Vilaprisan has entered clinical development and is currently undergoing phase 3 clinical trials.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Discovery of Vilaprisan (BAY 1002670): A Highly Potent and Selective Progesterone Receptor Modulator Optimized for Gynecologic Therapies ; volume:13 ; number:21 ; year:2018 ; pages:2271-2280 ; extent:10
ChemMedChem ; 13, Heft 21 (2018), 2271-2280 (gesamt 10)

Creator
Möller, Carsten
Bone, Wilhelm
Cleve, Arwed
Klar, Ulrich
Rotgeri, Andrea
Rottmann, Antje
Schultze‐Mosgau, Marcus‐Hillert
Wagenfeld, Andrea
Schwede, Wolfgang

DOI
10.1002/cmdc.201800487
URN
urn:nbn:de:101:1-2022090205521095025893
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:28 AM CEST

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Associated

  • Möller, Carsten
  • Bone, Wilhelm
  • Cleve, Arwed
  • Klar, Ulrich
  • Rotgeri, Andrea
  • Rottmann, Antje
  • Schultze‐Mosgau, Marcus‐Hillert
  • Wagenfeld, Andrea
  • Schwede, Wolfgang

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