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Not Yet RecruitingNCT07236931

Clinical Study of Selinexor-Based Chemotherapy With Minimal or No Cytotoxic Agents in Treatment-Naïve AML Patients Unsuitable for Intensive Therapy: Focusing on Rapid Reduction of Blast Cells

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
71 (estimated)
Sponsor
Donghua Zhang · Academic / Other
Sex
All
Age
18 Years – 74 Years
Healthy volunteers
Not accepted

Summary

This study aims to evaluate the efficacy and safety of selinexor-based chemotherapy-sparing regimens (including chemotherapy-free or dose-reduced approaches) in optimizing therapeutic strategies for treatment-naïve acute myeloid leukemia patients deemed unfit for intensive induction therapy. The investigation will focus on dynamic blast clearance patterns and early toxicity profiles to inform timely treatment adaptation during the critical induction window.

Conditions

Interventions

TypeNameDescription
DRUGthe XAB regimenthe XAB regimen: a chemotherapy-free or low-dose chemotherapy regimen containing selinexor (X), azacitidine (A), and venetoclax (B)

Timeline

Start date
2025-11-20
Primary completion
2027-10-20
Completion
2028-10-20
First posted
2025-11-19
Last updated
2025-11-19

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07236931. Inclusion in this directory is not an endorsement.

Clinical Study of Selinexor-Based Chemotherapy With Minimal or No Cytotoxic Agents in Treatment-Naïve AML Patients Unsui (NCT07236931) · Clinical Trials Directory