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Study identifier: NCT02416388 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study to Improve OS in 18 to 60 Year-old Patients, Comparing Daunorubicin Versus High Dose Idarubicin Induction Regimens, High Dose Versus Intermediate Dose Cytarabine Consolidation Regimens, and Standard Versus MMF Prophylaxis of GvHD in Allografted Patients in First CR

Condition: Acute Myeloid Leukemia (AML)  ·  Sponsor: University Hospital, Angers

PhasePhase 2/Phase 3
Planned participants3100
Who can joinAll sexes, 18 Years to 61 Years
Healthy volunteersNo

About this study

This open label, multicenter phase II/III study with multiple randomization phases at differents stages of AML treatment (induction, consolidation and HSCT where applicable) is designed to improve OS in younger (18 to 60 year-old) patients, with AML risk-adapted patient strategies. Within the intermediate risk AML group, optimal GvHD prophylaxis following allogeneic SCT in first CR, after either myeloablative (MAC) or reduced intensity (RIC) conditioning, will also be evaluated. With an adaptative design, this clinical trial could test up to 3 novel AML agents of interest.

This description comes directly from the study's public registry record.

Talk to the study team

Mathilde Hunault, PD  ·  MaHunault@chu-angers.fr

DRCI Promotion Interne  ·  + 33 2 41 35 68 28  ·  EcPromotionInterne@chu-angers.intra

Always discuss trial participation with your own doctor first.

Locations (56)

CH Amiens Hôpital SudAmiens, FranceRecruiting
CHU AngersAngers, FranceRecruiting
CH Victor DupouyArgenteuil, FranceRecruiting
Centre Hospitalier de la Côte BasqueBayonne, FranceRecruiting
Hôpital Jean MinjozBesançon, FranceRecruiting
CH BeziersBéziers, FranceRecruiting
Hôpital AvicenneBobigny, FranceRecruiting
CH BordeauxBordeaux, FranceRecruiting
Hôpital du Dr DuchenneBoulogne-sur-Mer, FranceRecruiting
Hôpital MorvanBrest, FranceRecruiting
CH CaenCaen, FranceRecruiting
Clinique du parcCastelnau-le-Lez, FranceWithdrawn

+ 44 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT02416388