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Completed Phase 1 Interventional

Selinexor With Combination Chemotherapy in Treating Patients With Acute Myeloid Leukemia

ClinicalTrials.gov ID: NCT02573363

Public ClinicalTrials.gov record NCT02573363. 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 7, 2026, 10:59 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

Phase I Investigator Sponsored Study to Assess the Tolerability and Efficacy of Selinexor in Combination With High Dose Cytarabine (HiDAC) and Mitoxantrone Chemotherapy for Remission Induction in Acute Myelogenous Leukemia (AML)

Study identification

NCT ID
NCT02573363
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
University of Chicago
Other
Enrollment
25 participants

Conditions and interventions

Interventions

  • Cytarabine Drug
  • Mitoxantrone Hydrochloride Drug
  • Selinexor Drug

Drug

Eligibility (public fields only)

Age range
Not listed
Sex
All
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
Oct 6, 2015
Primary completion
Dec 31, 2017
Completion
May 2, 2019
Last update posted
Apr 7, 2020

2015 – 2019

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02573363, 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 7, 2020 · Synced May 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02573363 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →