Condition: Endometrial Cancer · Sponsor: Karyopharm Therapeutics Inc
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.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| The University of Alabama at Birmingham | Birmingham, Alabama, United States | — |
| Honor Health | Phoenix, Arizona, United States | — |
| University of Arkansas for Medical Sciences | Little Rock, Arkansas, United States | — |
| UC DAVIS | Davis, California, United States | — |
| City of Hope National Medical Center | Duarte, California, United States | — |
| City of Hope at Irvine Lennar | Irvine, California, United States | — |
| Cancer and Blood Specialty Clinic | Los Alamitos, California, United States | — |
| UCLA - Women's Health Clinical Research Unit | Los Angeles, California, United States | — |
| Long Beach Memorial Medical Center | Los Angeles, California, United States | — |
| Stanford University | Palo Alto, California, United States | — |
| California Pacific Medical Center | San Francisco, California, United States | — |
| Broward Health Medical Center | Fort Lauderdale, Florida, United States | — |
+ 192 more locations — full list on the registry record.
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