An Open-label, First-in-human, Dose Escalation Study of SAR440234 Administered as Single Agent by Intravenous Infusion in Patients With Relapsed or Refractory Acute Myeloid Leukemia (R/R AML), B-cell Acute Lymphoblastic Leukemia (B-ALL), or High Risk Myelodysplasia (HR-MDS)

Status: Discontinued

Phase of Trial: Phase I/II

Latest Information Update: 08 Apr 2022

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At a glance

Drugs SAR-440234 (Primary)
Indications Acute myeloid leukaemia; Myelodysplastic syndromes; Precursor B-cell lymphoblastic leukaemia-lymphoma
Focus Adverse reactions; First in man; Therapeutic Use
Sponsors Sanofi

Most Recent Events

08 Jul 2021 Status changed from recruiting to discontinued.
03 May 2021 This trial has been Discontinued in France, according to European Clinical Trials Database record.
26 Mar 2021 Planned End Date changed from 1 Aug 2023 to 1 Sep 2023.

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