Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
NOT YET RECRUITING
NCT06297772
PHASE3

Compare the Efficacy and Safety of Dec-FB4 and FB4 as Conditioning Regimen for AML-MR

Sponsor: Ruijin Hospital

View on ClinicalTrials.gov

Summary

A multicenter, randomized, controlled clinical study comparing the efficacy and safety of allogeneic hematopoietic stem cell transplantation with decitabine-Fludarabine- busulfan (Dec-FB4) and Fludarabine-busulfan (FB4) as pretreatment regimens for the treatment of acute myeloid leukemia in adults with MR gene abnormalities

Official title: Comparing the Efficacy and Safety of Decitabine-Fludarabine-busulfan (Dec-FB4) and Fludarabine-busulfan (FB4) as Conditioning Regimens for AML-MR

Key Details

Gender

All

Age Range

16 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

220

Start Date

2024-06-01

Completion Date

2028-05-01

Last Updated

2024-06-04

Healthy Volunteers

No

Conditions

Interventions

DRUG

Decitabine

decitabine 20mg/m2 per day for consecutive 5 days

DRUG

Fludarabine Injection

fludarabine 30mg/m2 per day for consecutive 5 days

DRUG

Busulfan Injection

Busulfan 3.2mg/kg per day for consecutive 4 days

Locations (1)

Ruijin Hospital

Shanghai, China