Antiprogestin Pharmacodynamics, Pharmacokinetics, and Metabolism: Implications for Their Long-Term Use
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⤵ 3 in-corpus citations
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This review discusses the pharmacodynamics, pharmacokinetics, and metabolism of mifepristone, lilopristone, and onapristone, including their interactions with CYP3A4 and P-glycoprotein.
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Cites (4)
- Clinical efficacy of the antiprogesterone RU486 in the treatment of endometriosis and uterine fibroids 1994
- Comparison of Yuzpe regimen, danazol, and mifepristone (RU486) in oral postcoital contraception. 1992
- Regression of Uterine Leiomyomata in Response to the Antiprogesterone RU 486 1993
- Pharmacokinetics of mifepristone after low oral doses 1996
Cited by (3)
- Progesterone receptor ligands for the treatment of endometriosis: the mechanisms behind therapeutic success and failure 2020
- Population Pharmacokinetics of Telapristone (CDB-4124) and its Active Monodemethylated Metabolite CDB-4453, with a Mixture Model for Total Clearance 2011
- Novel class of non-steroidal progesterone receptor antagonists 1999
References (100)
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- Comparison of Yuzpe regimen, danazol, and mifepristone (RU486) in oral postcoital contraception. via openalex
- Pharmacokinetics of mifepristone after low oral doses via openalex
- Regression of Uterine Leiomyomata in Response to the Antiprogesterone RU 486 via openalex
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Cited by (3)
- Progesterone receptor ligands for the treatment of endometriosis: the mechanisms behind therapeutic success and failure 2020
- Population Pharmacokinetics of Telapristone (CDB-4124) and its Active Monodemethylated Metabolite CDB-4453, with a Mixture Model for Total Clearance 2011
- Novel class of non-steroidal progesterone receptor antagonists 1999
Source provenance
- europepmc
- last seen: 2026-06-11T06:19:48.454388+00:00
- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
- pubmed
- last seen: 2026-05-13T22:10:40.754221+00:00
License: CC0
· commercial use OK