Difference between revisions of "Volasertib (BI-6727)"

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(Created page with "=Mechanism of action= Polo-like kinase 1 ([http://www.genenames.org/cgi-bin/gene_symbol_report?hgnc_id=9077 PLK1]) inhibitor =Preliminary data= # Döhner H, Lübbert M, Fiedl...")
 
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=Preliminary data=
 
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==[[Acute myeloid leukemia]]==
 
# Döhner H, Lübbert M, Fiedler W, Fouillard L, Haaland A, Brandwein JM, Lepretre S, Reman O, Turlure P, Ottmann OG, Müller-Tidow C, Krämer A, Raffoux E, Döhner K, Schlenk RF, Voss F, Taube T, Fritsch H, Maertens J. Randomized, phase 2 trial comparing low-dose cytarabine with or without volasertib in AML patients not suitable for intensive induction therapy. Blood. 2014 Jul 8. [Epub ahead of print] [http://bloodjournal.hematologylibrary.org/content/early/2014/07/07/blood-2014-03-560557.long link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/25006120 PubMed]
 
# Döhner H, Lübbert M, Fiedler W, Fouillard L, Haaland A, Brandwein JM, Lepretre S, Reman O, Turlure P, Ottmann OG, Müller-Tidow C, Krämer A, Raffoux E, Döhner K, Schlenk RF, Voss F, Taube T, Fritsch H, Maertens J. Randomized, phase 2 trial comparing low-dose cytarabine with or without volasertib in AML patients not suitable for intensive induction therapy. Blood. 2014 Jul 8. [Epub ahead of print] [http://bloodjournal.hematologylibrary.org/content/early/2014/07/07/blood-2014-03-560557.long link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/25006120 PubMed]
  

Revision as of 04:20, 21 November 2014

Mechanism of action

Polo-like kinase 1 (PLK1) inhibitor

Preliminary data

Acute myeloid leukemia

  1. Döhner H, Lübbert M, Fiedler W, Fouillard L, Haaland A, Brandwein JM, Lepretre S, Reman O, Turlure P, Ottmann OG, Müller-Tidow C, Krämer A, Raffoux E, Döhner K, Schlenk RF, Voss F, Taube T, Fritsch H, Maertens J. Randomized, phase 2 trial comparing low-dose cytarabine with or without volasertib in AML patients not suitable for intensive induction therapy. Blood. 2014 Jul 8. [Epub ahead of print] link to original article PubMed

History of changes in FDA indication