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Acute myeloid leukaemia (AML)

Volasertib, Boehringer Ingelheim´s investigational treatment of acute myeloid leukaemia, is granted ‘orphan drug designation’ in the EU and the US

17 April 2014 | By Boehringer Ingelheim

Boehringer Ingelheim announced that the US Food and Drug Administration and the European Commission have granted volasertib* ‘orphan drug designation' for the treatment of patients with acute myeloid leukaemia...

Prof. Klaus Dugi, Corporate Senior Vice President Medicine, Boehringer Ingelheim

news

Volasertib receives FDA Breakthrough Therapy designation for treatment of patients with acute myeloid leukaemia

17 September 2013 | By Boehringer Ingelheim

Administration (FDA) to potentially provide a new treatment option to improve survival related outcomes for patients with acute myeloid leukaemia (AML)...

news

Boehringer Ingelheim announces initiation of pivotal trial investigating volasertib* in patients with acute myeloid leukaemia

28 February 2013 | By Boehringer Ingelheim

Boehringer Ingelheim invests in rare diseases...

news

New phase II data demonstrates significant activity of quizartinib in relapsed or refractory acute myeloid leukaemia (AML) patients1,2

10 December 2012 | By Red Consultancy

Results from a completed phase II study...

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Recommended

Acute myeloid leukaemia (AML)

Volasertib, Boehringer Ingelheim´s investigational treatment of acute myeloid leukaemia, is granted ‘orphan drug designation’ in the EU and the US

Volasertib receives FDA Breakthrough Therapy designation for treatment of patients with acute myeloid leukaemia

Boehringer Ingelheim announces initiation of pivotal trial investigating volasertib* in patients with acute myeloid leukaemia

New phase II data demonstrates significant activity of quizartinib in relapsed or refractory acute myeloid leukaemia (AML) patients1,2