Efficacy and Safety of MTBF Conditioning Regimen for Salvageable Allo-HSCT in the Treatment of R/R AML

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorFirst Affiliated Hospital Xi'an Jiaotong University

About this trial

The primary objective of this study was to evaluate the efficacy of MTBF conditioning regimen of salvageable allo-HSCT in patients with relapsed or refractory acute myeloid leukemia. The secondary purpose of the study was to observe the safety of MTBF regimen in these patients.

Eligibility criteria

Qualifiers

The subjects voluntarily joined the study, signed the informed consent, had good compliance, and cooperated with the follow-up;

Age 18-65 years old (including upper and lower limits);

No gender limitation

Relapsed or refractory (R/R) acute myeloid leukemia can not achieve complete remission by chemotherapy, and has the indication of salvage allogeneic hematopoietic stem cell transplantation.

Disqualifiers

Hypersensitivity to any investigational drug or its components;

Uncontrolled systemic diseases (e.g. active infections, uncontrolled hypertension, diabetes, etc.)

Long QTc syndrome or QTc interval>480 ms;

Complete left bundle branch block, II or III degree atrioventricular block;

Trial design

Treatments tested in this trial

  • MTBF regimen

Treatment groups

37 Participants
are divided into 1 treatment group

Locations

This trial has no locations