ClinicalTrials.gov record
Completed Phase 3 Interventional

Maintenance With Selinexor/Placebo After Combination Chemotherapy in Participants With Endometrial Cancer [SIENDO]

ClinicalTrials.gov ID: NCT03555422

Public ClinicalTrials.gov record NCT03555422. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 10:02 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Phase 3 Trial of Maintenance With Selinexor/ Placebo After Combination Chemotherapy for Patients With Advanced or Recurrent Endometrial Cancer

Study identification

NCT ID
NCT03555422
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Karyopharm Therapeutics Inc
Industry
Enrollment
263 participants

Conditions and interventions

Interventions

  • Matching placebo for selinexor Drug
  • Selinexor Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 4, 2018
Primary completion
Jan 21, 2022
Completion
Apr 2, 2025
Last update posted
Apr 12, 2026

2018 – 2025

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Arizona Oncology Tucson Arizona 85711
Stanford University Palo Alto California 94304
Moffitt Cancer Center Tampa Florida 33612
Florida Cancer Specialists (Sarah Cannon Research Institute) West Palm Beach Florida 33401
Gynecological Cancer Institute of Chicago Oak Lawn Illinois 60453
Parkview Research Center Fort Wayne Indiana 46845
Indiana University Simon Cancer Center Indianapolis Indiana 46202
HCA Midwest Health - Kansas City (Sarah Cannon Research Institute) Kansas City Missouri 64132
NYU Langone New York New York 10016
Memorial Sloan Kettering Cancer Center New York New York 10065
University of Oklahoma Health Sciences Center - Stephenson Cancer Center Oklahoma City Oklahoma 73104
Oncology Associates of Oregon Eugene Oregon 97401
Women & Infants Hospital of Rhode Island Providence Rhode Island 02905
Tennessee Oncology Nashville (Sarah Cannon Research Institute) Nashville Tennessee 37203
Texas Oncology, Austin Austin Texas 78731
Texas Oncology DFW Dallas Texas 75246
University of Texas Southwestern Medical Center Dallas Texas 75390
Texas Oncology DFW Fort Worth Texas 76104
VCU Massey Cancer Center Richmond Virginia 23298

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 59 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03555422, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 12, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03555422 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →