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Study identifier: NCT05611931 Synced from ClinicalTrials.gov · August 03, 2026
● Active Not Recruiting

Selinexor in Maintenance Therapy After Systemic Therapy for Participants With p53 Wild-Type, Advanced or Recurrent Endometrial Carcinoma

Condition: Endometrial Cancer  ·  Sponsor: Karyopharm Therapeutics Inc

PhasePhase 3
Planned participants257
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the efficacy and safety of selinexor as a maintenance treatment in patients with p53 wt endometrial carcinoma (EC), who have achieved a partial response (PR) or complete response (CR) (per Response Evaluation Criteria in Solid Tumors version 1.1 \[RECIST v 1.1\]) after completing at least 12 weeks of platinum-based therapy. A total of 276 participants will be enrolled in the study and randomized in a 1:1 ratio to maintenance therapy with either selinexor or placebo.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

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Locations (204)

The University of Alabama at BirminghamBirmingham, Alabama, United States
Honor HealthPhoenix, Arizona, United States
University of Arkansas for Medical SciencesLittle Rock, Arkansas, United States
UC DAVISDavis, California, United States
City of Hope National Medical CenterDuarte, California, United States
City of Hope at Irvine LennarIrvine, California, United States
Cancer and Blood Specialty ClinicLos Alamitos, California, United States
UCLA - Women's Health Clinical Research UnitLos Angeles, California, United States
Long Beach Memorial Medical CenterLos Angeles, California, United States
Stanford UniversityPalo Alto, California, United States
California Pacific Medical CenterSan Francisco, California, United States
Broward Health Medical CenterFort Lauderdale, Florida, United States

+ 192 more locations — full list on the registry record.

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