RecruitingPhase 2NCT05917405

Study Comparing the Efficacy of 2 RIC Regimens (Clofarabine vs Fludarabine) in Adults With AML Eligible to Allo-SCT

FLUCLORIC: Randomized Multicentric Phase III Study Comparing the Efficacy of 2 Reduced Intensity Conditioning Regimens (Clofarabine/Busulfan vs Fludarabine/Busulfan) in Adults With AML and Eligible to Allogeneic Stem Cell Transplantation


Sponsor

Nantes University Hospital

Enrollment

302 participants

Start Date

Sep 14, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 99 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing two different reduced-intensity chemotherapy regimens — clofarabine vs. fludarabine — used before a stem cell transplant (allo-SCT) in adults with AML (acute myeloid leukemia) or MDS (a pre-leukemia bone marrow disorder) who are in remission. **You may be eligible if...** - You are 18 or older - You have AML or MDS and are in remission (bone marrow blasts under 5%) - You are eligible for a reduced-intensity transplant (age 60+, or younger with health conditions that prevent full-intensity conditioning) - A matched donor (related or unrelated) is available for you **You may NOT be eligible if...** - Your disease is not in remission at the time of transplant - You have severe heart, lung, or liver problems - You are pregnant or breastfeeding - A suitable donor is not available Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGFludarabine

30 mg/m2/day IV fludarabine for 5 days (day-6 to day-2)

DRUGBusulfan

130 mg/m2/day IV busulfan once daily for 2 days (day -4 and -3)

DRUGATG

Thymoglobuline®: 2.5 mg/Kg/day IV for 2 consecutive days (day -2 and -1)

DRUGClofarabine

30 mg/m2/day IV clofarabine for 5 days (day-6 to day-2)


Locations(23)

CHU de Nantes

Nantes, Loire Atlantique, France

CHU Amiens

Amiens, France

CHU Angers

Angers, France

CHU Besançon

Besançon, France

CHU Bordeaux

Bordeaux, France

CHU Brest

Brest, France

CRLC Caen

Caen, France

CHU Clermont-Ferrand

Clermont-Ferrand, France

APHP Créteil

Créteil, France

CHU Grenoble

Grenoble, France

CHRU Lille

Lille, France

CHU Limoges

Limoges, France

CHU Lyon

Lyon, France

Institut Paoli Calmettes

Marseille, France

CHU Montpellier

Montpellier, France

CHRU Nancy

Nancy, France

CHU Paris St-Louis

Paris, France

Pitie-Salpetriere, APHP

Paris, France

St-Antoine, APHP

Paris, France

CHU Poitiers

Poitiers, France

CHU Rennes

Rennes, France

CHU St-Etienne

Saint-Etienne, France

CRLC Toulouse

Toulouse, France

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NCT05917405


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