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A Phase 1, Open Label, Dose Escalation, and Dose Expansion Study to Assess the Safety, Tolerability, and Preliminary Antileukemic Activity of GDX012 in Patients With Minimal Residual Disease (MRD) Positive Acute Myeloid Leukemia

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A Phase 1, Open Label, Dose Escalation, and Dose Expansion Study to Assess the Safety, Tolerability, and Preliminary Antileukemic Activity of GDX012 in Patients With Minimal Residual Disease (MRD) Positive Acute Myeloid Leukemia

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 22 Jul 2022

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At a glance

  • Drugs TAK 012 (Primary) ; Cyclophosphamide; Fludarabine
  • Indications Acute myeloid leukaemia
  • Focus Adverse reactions; First in man
  • Sponsors GammaDelta Therapeutics

    • Most Recent Events

    • 18 Jul 2022 Status changed from recruiting to discontinued.
    • 13 Apr 2022 Trial design presented at the 113th Annual Meeting of the American Association for Cancer Research.
    • 15 Sep 2021 According to a GammaDelta Therapeutics media release, First dose delivered to patients of this study.

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