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Clinical Trial Summary

This clinical trial studies the efficacy and safety of selinexor combined with HAD or CAG regimen in the treatment of relapsed or refractory acute myeloid leukemia


Clinical Trial Description

Main Purpose: To observe the efficacy of selinexor in combination with HAD or CAG regimen for relapsed and refractory acute myeloid leukemia :complete remission rate (CR rate), partial remission rate (PR rate), no remission rate (NR rate), complete remission with incomplete hematologic recovery(CRi rate) Secondary Purposes: 1. To observe the recurrence rate of selinexor combined with HAD or CAG regimen for relapsed and refractory acute myeloid leukemia, treatment-related mortality(TRM), Overall Survival (OS), Event-Free Survival (EFS); 2. Safety indicators: to observe adverse events and deaths during treatment with selinexor in combination with HAD or CAG regimen. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05726110
Study type Interventional
Source Shanxi Bethune Hospital
Contact Tao Wang
Phone 13835175119
Email wangtao99699@163.com
Status Recruiting
Phase Phase 3
Start date January 29, 2023
Completion date December 31, 2024

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