OncoMatch/Clinical Trials/NCT05917405
Study Comparing the Efficacy of 2 RIC Regimens (Clofarabine vs Fludarabine) in Adults With AML Eligible to Allo-SCT
Is NCT05917405 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Fludarabine and Busulfan for acute myeloid leukemia in remission.
Treatment: Fludarabine · Busulfan · ATG · Clofarabine — Relapse remains the main cause of death in patients with myeloid malignancies, especially after an allotransplant. Using drugs with higher anti-leukemic activity as part of the conditioning regimen is one of the strategies to decrease relapse incidence in this population. Retrospective studies have shown that clofarabine can achieve impressive results compared to the use of fludarabine in acute myeloid leukemia (AML) as part of the conditioning regimen. Confirming such results in a prospective manner would definitely establish the CloB2A2 as a superior reduced-intensity conditioning (RIC) regimen compared to the FB2A2 for AML patients.302 AML patients (151 in each arm) in complete remission at transplant will be included with the main objective to demonstrate a significant better 2-year overall survival for CloB2A2 cases (70% vs 55%). A cost-utility analysis and a cost-effectiveness analysis will be also performed as well as an assessment of the quality of life after transplant. Clofarabine will be furnished to all centers. The duration of the study will be 5 years with 3 years of inclusion and 2 years of follow-up for each patient.
Check if I qualifyExtracted eligibility criteria
Cancer type
Acute Myeloid Leukemia
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Lab requirements
Kidney function
creatinine clearance < 50 ml/min (evaluated by mdrd or ckdepi) [excluded]
Liver function
serum bilirubine > 30 mmol/l, cytolysis > 5 the upper limit range [excluded]
Cardiac function
left ventricular ejection fraction < 50% [excluded]
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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