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Clinical Trial Summary

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 220 participants will be enrolled in the study and randomized in a 1:1 ratio to maintenance therapy with either selinexor or placebo.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05611931
Study type Interventional
Source Karyopharm Therapeutics Inc
Contact Karyopharm Medical Information
Phone (888) 209-9326
Email clinicaltrials@karyopharm.com
Status Recruiting
Phase Phase 3
Start date April 18, 2023
Completion date January 31, 2028

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