Introduction: Ivosidenib is an inhibitor of mutant isocitrate dehydrogenase 1 (mIDH1) that is approved alone or in combination with azacitidine in patients with mIDH1 acute myeloid leukemia (AML) that are ineligible to receive intensive chemotherapy. Aims: Here we describe the design of ALIDHE, an international, multicenter, single-arm, open-label Phase 3b study of ivosidenib + azacitidine for treatment of newly diagnosed mIDH1 AML in usual clinical practice. Methods: The primary endpoints are adverse events (AEs), clinical laboratory anomalies assessed as AEs, patients requiring transfusion and number of units transfused, and infection rate. The impact of ivosidenib + azacitidine treatment on health-related quality of life, healthcare resource utilization and measurable residual disease will also be assessed. Clinical trial registration number: NCT05907057 (ClinicalTrials.gov).

Vyas, P., Salek, S., Vives, S., Recher, C., Döhner, H., Venditti, A., et al. (2025). ALIDHE phase 3b study design: ivosidenib + azacitidine in adults with newly diagnosed IDH1 mutant acute myeloid leukemia. FUTURE ONCOLOGY, 1-9 [10.1080/14796694.2025.2567838].

ALIDHE phase 3b study design: ivosidenib + azacitidine in adults with newly diagnosed IDH1 mutant acute myeloid leukemia

Venditti, Adriano
Writing – Review & Editing
;
2025-11-15

Abstract

Introduction: Ivosidenib is an inhibitor of mutant isocitrate dehydrogenase 1 (mIDH1) that is approved alone or in combination with azacitidine in patients with mIDH1 acute myeloid leukemia (AML) that are ineligible to receive intensive chemotherapy. Aims: Here we describe the design of ALIDHE, an international, multicenter, single-arm, open-label Phase 3b study of ivosidenib + azacitidine for treatment of newly diagnosed mIDH1 AML in usual clinical practice. Methods: The primary endpoints are adverse events (AEs), clinical laboratory anomalies assessed as AEs, patients requiring transfusion and number of units transfused, and infection rate. The impact of ivosidenib + azacitidine treatment on health-related quality of life, healthcare resource utilization and measurable residual disease will also be assessed. Clinical trial registration number: NCT05907057 (ClinicalTrials.gov).
15-nov-2025
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/15
Settore MEDS-09/B - Malattie del sangue
English
Con Impact Factor ISI
Acute myeloid leukemia; azacitidine; healthcare utilization; ivosidenib; mutant isocitrate dehydrogenase 1; quality of life
This study was sponsored by Servier Affaires Médicales, France. ServierAffaires Médicales Servier Affaires Médicales 35 rue de Verdun 92284Suresnes CEDEX. Role of trial sponsor: responsible for the design of thestudy; collection, management, analysis, and interpretation of data; thedecision to submit this report for publication. The sponsor had ultimateauthority over these activities
https://doi.org/10.1080/14796694.2025.2567838
Vyas, P., Salek, S., Vives, S., Recher, C., Döhner, H., Venditti, A., et al. (2025). ALIDHE phase 3b study design: ivosidenib + azacitidine in adults with newly diagnosed IDH1 mutant acute myeloid leukemia. FUTURE ONCOLOGY, 1-9 [10.1080/14796694.2025.2567838].
Vyas, P; Salek, S; Vives, S; Recher, C; Döhner, H; Venditti, A; Derrien, H; Chatin, S; De La Bigne, A; Pelouchova, J; Hills, R; Nier, S
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/439924
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