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A Phase II, Multi-Center, Open-Label, Repeat-Dose Study of Forodesine Hydrochloride (BCX-1777) Infusion in Patients with Advanced T-Cell Leukemia with an Option of Long-Term Forodesine Hydrochloride (...

Update Il y a 4 ans
Reference: EUCTR2004-004286-15

A Phase II, Multi-Center, Open-Label, Repeat-Dose Study of Forodesine Hydrochloride (BCX-1777) Infusion in Patients with Advanced T-Cell Leukemia with an Option of Long-Term Forodesine Hydrochloride (BCX-1777) Use

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Extract

To determine the sustained effectiveness (for a minimum of 28 days) of intravenous (IV) forodesine hydrochloride infusions in patients with advanced T-cell leukemia (precursor T-lymphoblastic leukemia/lymphoma or T-cell prolymphocytic leukemia [T-PLL])

Inclusion criteria

  • Advanced T-cell Leukaemia (either T-cell Acute Lymphoblastic Leukaemia [T-ALL] or T-cell Prolymphocytic Leukaemia [T-PLL]) or Aleukaemic Leukaemia

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