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A Phase I/2 Dose Escalation Safety, Pharmacokinetic and Efficacy Study of Multiple Intravenous Administrations of a Humanized Monoclonal Antibody (SAR650984) Against CD38 in Patients With Selected CD38+ Hematological Malignancies

Trial Profile

A Phase I/2 Dose Escalation Safety, Pharmacokinetic and Efficacy Study of Multiple Intravenous Administrations of a Humanized Monoclonal Antibody (SAR650984) Against CD38 in Patients With Selected CD38+ Hematological Malignancies

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 25 Sep 2024

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At a glance

  • Drugs Dexamethasone (Primary) ; Dexamethasone (Primary) ; Isatuximab (Primary)
  • Indications Acute myeloid leukaemia; B-cell lymphoma; Chronic lymphocytic leukaemia; Multiple myeloma; Non-Hodgkin's lymphoma; Precursor cell lymphoblastic leukaemia-lymphoma
  • Focus Adverse reactions; First in man; Therapeutic Use
  • Sponsors Sanofi; Sanofi Aventis Deutschland GmbH; Sanofi-Aventis Recherche & Developpement
  • Most Recent Events

    • 05 Oct 2023 Status changed from active, no longer recruiting to completed.
    • 10 Aug 2023 This trial has been completed in Finland (End Date: 13 Jul 2023), according to European Clinical Trials Database record.
    • 07 Jul 2023 Planned End Date changed from 30 Aug 2023 to 14 Jul 2023.

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