A Phase I/II open label study to assess efficacy and safety of IPH1101 associated with low dose of interleukin 2, as add-on therapy to imatinib in CML patients with residual molecular disease

Update Il y a 4 ans
Reference: EUCTR2007-004252-37

Woman and Man

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Extract

The primary objective is to assess the efficacy of IPH1101 associated with low dose of IL-2 as add-on therapy to imatinib in CML patients with residual molecular disease after at least 2 years of imatinib monotherapy.


Inclusion criteria

  • Chronic myeloid leukemia

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