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Ibrutinib

Known as: 1-[(3R)-3-[4-Amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl]prop-2-en-1-one, 2-Propen-1-one, 1-((3R)-3-(4-amino-3-(4-phenoxyphenyl)-1h-pyrazolo(3,4-d)pyrimidin-1-yl)-1-piperidinyl)- 
An orally bioavailable, small-molecule inhibitor of Bruton's tyrosine kinase (BTK) with potential antineoplastic activity. Upon oral administration… 
National Institutes of Health

Papers overview

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Review
2018
Review
2018
BACKGROUND: Chronic lymphocytic leukemia (CLL) is one of the most common lymphoid malignancies, accounting for ~11% of all… 
2018
2018
7502Background: Ibr, a first-in-class, once-daily BTK inhibitor, is approved in the US and EU for CLL treatment, including del17p… 
Highly Cited
2017
Highly Cited
2017
Orphan Nano drugs such as Rituxan, Revlimid, Soliris, Afinitor, Tasigna, Velcade, Avonex, Alimta, Yervoy, Sprycel, Rebif… 
2017
2017
7509Background: Immunotherapy with anti-CD19 CART cells induces complete remission (CR) in the minority of patients with CLL, but… 
2017
2017
Background: Ibrutinib (IBR), a BTK inhibitor is approved for patients (pts) with CLL. Venetoclax (VEN), a BCL2 inhibitor is… 
2016
2016
Progressive multifocal leukoencephalopathy (PML) is a devastating neurological disease observed nearly exclusively in… 
2015
2015
Introduction In 2 large phase 3 trials of patients (pts) with relapsed or refractory (R/R) CLL/SLL, single-agent ibrutinib (ibr… 
Review
2014
Review
2014
Abstract Recent clinical data suggest remarkable activity of ibrutinib, the first-in-class covalent inhibitor of Bruton's… 
2013
2013
![Graphic][1] The Bruton tyrosine kinase (BTK) inhibitor ibrutinib is a promising new targeted therapy for patients with mature…