Vilaprisan for the treatment of symptomatic endometriosis: results from a terminated phase 2b randomized controlled trial

dc.contributor.authorTaylor H.S.
dc.contributor.authorDong L.
dc.contributor.authorHaikonen J.
dc.contributor.authorOppelt P.
dc.contributor.authorTamussino K.
dc.contributor.authorWenzl R.
dc.contributor.authorFaustmann T.
dc.contributor.authorGroettrup-Wolfers E.
dc.contributor.authorRen X.
dc.contributor.authorSeitz C.
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.converis.publication-id404721911
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/404721911
dc.date.accessioned2025-08-28T00:30:23Z
dc.date.available2025-08-28T00:30:23Z
dc.description.abstract<p><strong>Objective: </strong>To evaluate the efficacy and safety of 2 doses of vilaprisan vs. placebo in participants with symptomatic endometriosis.</p><p><strong>Design: </strong>Multicenter, randomized, double-blind, placebo-controlled, parallel-group phase 2b trial (NCT03573336). The initially planned sample size was 315 patients. Recruitment was paused to assess long-term toxicity findings in rodents; although the findings were assessed as likely to be of limited clinical relevance in humans, the study was closed by the sponsor. During the pause, enrolled patients completed 3 or 6 months of treatment per their assigned regimen.</p><p><strong>Setting: </strong>University hospitals, a regional hospital, and a private clinic.</p><p><strong>Patients: </strong>Premenopausal adults with confirmed endometriosis and moderate-to-severe pelvic pain (≥4/10 on a numerical rating scale) were enrolled. Inclusion required protocol adherence, including ≥24 diary entries, and an average pain score of ≥3.5.</p><p><strong>Intervention: </strong>Participants were randomly assigned 1:1:1 to receive vilaprisan (2 mg), vilaprisan (4 mg), or placebo.</p><p><strong>Main outcome measures: </strong>The primary outcome was a change in the 7-day mean "worst pain" (per the endometriosis symptom diary item 1) from baseline to month 3. All analyses were descriptive only.</p><p><strong>Results: </strong>Eight participants were randomly assigned to treatment before the study pause: 6 received vilaprisan (4 mg, n = 4 and 2 mg, n = 2), and 2 received placebo. The 6 vilaprisan recipients experienced an improvement in endometriosis-associated pelvic pain, whereas the 2 placebo recipients experienced no change or increased pain; all 8 participants had decreased use of pain medication. Bleeding intensity decreased from baseline in the vilaprisan group.</p><p><strong>Conclusion: </strong>The study findings suggest that vilaprisan may improve outcomes in patients with endometriosis. Further studies in larger populations would be needed to accurately assess treatment effects.</p>
dc.format.pagerange189
dc.format.pagerange196
dc.identifier.jour-issn2666-3341
dc.identifier.olddbid205835
dc.identifier.oldhandle10024/188862
dc.identifier.urihttps://www.utupub.fi/handle/11111/34966
dc.identifier.urlhttps://doi.org/10.1016/j.xfre.2024.03.002
dc.identifier.urnURN:NBN:fi-fe2025082791060
dc.language.isoen
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3123 Gynaecology and paediatricsen_GB
dc.okm.discipline3123 Naisten- ja lastentauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier Inc.
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1016/j.xfre.2024.03.002
dc.relation.ispartofjournalF&S Reports
dc.relation.issue2
dc.relation.volume5
dc.source.identifierhttps://www.utupub.fi/handle/10024/188862
dc.titleVilaprisan for the treatment of symptomatic endometriosis: results from a terminated phase 2b randomized controlled trial
dc.year.issued2024

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