Selective progesterone receptor modulators for the treatment of dysmenorrhea: an update

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This review examines clinical trials and observational studies evaluating selective progesterone receptor modulators for treating dysmenorrhea associated with endometriosis, adenomyosis, and uterine fibroids.

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AI-generated deep summary by claude@2026-06, 2026-06-09 · read from full text

This paper is an update review examining clinical trials and observational studies of selective progesterone receptor modulators (SPRMs) used to treat dysmenorrhea in patients with uterine diseases, focusing on how different SPRMs act on progesterone receptors with agonist, antagonist, or mixed effects across tissues. It summarizes that mifepristone, telapristone acetate, and vilaprisan show antagonistic activity, while ulipristal acetate and asoprisnil show both antagonist and partial agonist effects, and notes that evaluations have been conducted for endometriosis-, adenomyosis-, and uterine fibroid-related dysmenorrhea, with no studies reported for primary dysmenorrhea. A major caveat highlighted is that side effects and long-term safety concerns, including hepatotoxicity and PAECs, limit SPRM use. Relevance to endometriosis: the review specifically discusses SPRMs (including mifepristone, ulipristal acetate, and asoprisnil) as evaluated for dysmenorrhea related to endometriosis, and also covers adenomyosis-related dysmenorrhea.

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Abstract

INTRODUCTION: Dysmenorrhea is a painful symptom associated with uterine contractions and menstrual bleeding and is treated by administering analgesic drugs. Since progesterone receptors (PRs) have a major role in regulating uterine tissues (myometrium and endometrium) physiology, oral contraceptives are used off-label for treating primary or secondary dysmenorrhea. The development of selective progesterone receptor modulators (SPRMs), a class of synthetic steroids with agonistic, antagonistic, or mixed effects in targeting PRs in different tissues, stimulated their possible clinical use for treating secondary dysmenorrhea related to uterine diseases (endometriosis, adenomyosis, uterine fibroids). AREAS COVERED: The present review examines the development of the clinical trials and observational studies done with the different SPRMs for the treatment of dysmenorrhea in patients with uterine diseases. EXPERT OPINION: Mifepristone, telapristone acetate and vilaprisan have antagonistic activity on PRs, whereas ulipristal acetate and asoprisnil have both potent antagonist and partial agonist effects.Since no studies have been done on primary dysmenorrhea, the different SPRMs have been evaluated in the treatment of endometriosis, adenomyosis and uterine fibroid-related dysmenorrhea.
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ABSTRACT Introduction Dysmenorrhea is a painful symptom associated with uterine contractions and menstrual bleeding and is treated by administering analgesic drugs. Since progesterone receptors (PRs) have a major role in regulating uterine tissues (myometrium and endometrium) physiology, oral contraceptives are used off-label for treating primary or secondary dysmenorrhea. The development of selective progesterone receptor modulators (SPRMs), a class of synthetic steroids with agonistic, antagonistic, or mixed effects in targeting PRs in different tissues, stimulated their possible clinical use for treating secondary dysmenorrhea related to uterine diseases (endometriosis, adenomyosis, uterine fibroids). Areas covered The present review examines the development of the clinical trials and observational studies done with the different SPRMs for the treatment of dysmenorrhea in patients with uterine diseases. Expert opinion Mifepristone, telapristone acetate and vilaprisan have antagonistic activity on PRs, whereas ulipristal acetate and asoprisnil have both potent antagonist and partial agonist effects. Since no studies have been done on primary dysmenorrhea, the different SPRMs have been evaluated in the treatment of endometriosis, adenomyosis and uterine fibroid-related dysmenorrhea. Article highlights Progesterone is a central target for therapeutic interventions in the context of uterine diseases. There are no studies on the clinical use of SPRMs for the treatment of primary dysmenorrhea. Studies on SPRMs’ use for treating endometriosis-, adenomyosis-, and uterine fibroids-related dysmenorrhea are available (mifepristone, ulipristal acetate, asoprisnil, telapristone acetate, vilaprisan). The ability to selectively modulate progesterone activity without inducing hypoestrogenism makes SPRMs an attractive option for long-term treatment. Side effects and long-term safety (hepatotoxicity and PAECs) represent the major limit for SPRMs use. Declaration of interest The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties. Reviewer disclosure Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.

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Condition tags

mesh:D004412mesh:D004715endometriosisadenomyosisdysmenorrhea

MeSH descriptors

Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea Dysmenorrhea

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europepmc
last seen: 2026-06-04T01:30:01.192114+00:00
pubmed
last seen: 2026-06-02T00:32:06.746407+00:00
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last seen: 2026-05-11T08:34:28.763810+00:00
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