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AXL Inhibitor BGB324
Known as:
BGB324
An orally available and selective inhibitor of the AXL receptor tyrosine kinase (UFO), with potential antineoplastic activity. Upon administration…
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National Institutes of Health
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Related topics
Related topics
2 relations
NCIt Antineoplastic Agent Terminology
Receptor Tyrosine Kinase Inhibition
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A phase II study of bemcentinib (BGB324), a first-in-class highly selective AXL inhibitor, with pembrolizumab in pts with advanced NSCLC: OS for stage I and preliminary stage II efficacy.
E. Felip
,
P. Brunsvig
,
+17 authors
M. Krebs
Journal of Clinical Oncology
2019
Corpus ID: 198242242
9098 Background: AXL is an RTK implicated in epithelial-to-mesenchymal transition and as a resistance mechanism to multiple…
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Review
2018
Review
2018
The Role of the TAM Family of Receptor Tyrosine Kinases in Neural Development and Disorders
Jun Zhang
,
Xin Qi
2018
Corpus ID: 13710361
Tyrosine kinase receptor 3 (Tyro3), Axl, and Mer constitute the TAM family of receptor tyrosine kinases. These receptor tyrosine…
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2018
2018
Combination of bemcentinib (BGB324): A first-in-class selective oral AXL inhibitor, with pembrolizumab in patients with triple negative breast cancer and adenocarcinoma of the lung.
M. Yule
,
K. Davidsen
,
+15 authors
J. Lorens
2018
Corpus ID: 80056333
TPS43Background: Activation of the receptor tyrosine kinase AXL has a profound suppressive effect on the innate immune system…
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2018
2018
Phase II open-label, multi-centre study of bemcentinib (BGB324), a first-in-class selective AXL inhibitor, in combination with pembrolizumab in patients with advanced NSCLC.
J. Lorens
,
C. Arce-Lara
,
+14 authors
M. Chisamore
2018
Corpus ID: 80851225
3078Background: Bemcentinib (BGB324) is a first-in-class, oral, potent and highly selective inhibitor of the AXL tyrosine kinase…
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2018
2018
A randomized phase Ib/II study of the selective small molecule axl inhibitor bemcentinib (BGB324) in combination with either dabrafenib/trametinib or pembrolizumab in patients with metastatic…
O. Straume
,
C. Schuster
,
G. Gausdal
,
J. Lorens
,
B. Gjertsen
2018
Corpus ID: 81918991
9548Background: Upregulation of the receptor tyrosine kinase Axl has been linked with both a reduced response to PD-1 blockade…
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2018
2018
Abstract 3774: BGB324, a selective small-molecule inhibitor of receptor tyrosine kinase AXL, targets tumor immune suppression and enhances immune checkpoint inhibitor efficacy
K. Davidsen
,
K. Wnuk-Lipinska
,
+14 authors
J. Lorens
Immunology
2018
Corpus ID: 81290286
The AXL receptor tyrosine kinase is associated with poor overall survival in a wide spectrum of cancers. AXL signaling is…
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2017
2017
Abstract 626: BGB324, a selective small molecule inhibitor of receptor tyrosine kinase AXL, abrogates tumor intrinsic and microenvironmental immune suppression and enhances immune checkpoint…
K. Wnuk-Lipinska
,
K. Davidsen
,
+16 authors
J. Lorens
2017
Corpus ID: 80341852
The AXL receptor tyrosine kinase is associated with poor overall survival in a wide spectrum of cancers including lung and breast…
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2016
2016
Axl Blockade by BGB324 Inhibits BCR-ABL Tyrosine Kinase Inhibitor–Sensitive and -Resistant Chronic Myeloid Leukemia
I. Ben-Batalla
,
R. Erdmann
,
+19 authors
S. Loges
Clinical Cancer Research
2016
Corpus ID: 3464263
Purpose: BCR-ABL kinase inhibitors are employed successfully for chronic myeloid leukemia (CML) treatment. However, resistant…
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2016
2016
Implication of the Receptor Tyrosine Kinase AXL in Head and Neck Cancer Progression
Anne von Mässenhausen
,
J. Brägelmann
,
+9 authors
S. Perner
International Journal of Molecular Sciences
2016
Corpus ID: 7385412
Head and neck squamous cell carcinoma (HNSCC) remains a clinical challenge and identification of novel therapeutic targets is…
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2015
2015
Axl inhibition: a potential road to a novel acute myeloid leukemia therapy?
M. Janning
,
I. Ben-Batalla
,
S. Loges
Expert Review of Hematology
2015
Corpus ID: 24669185
Novel treatment options in acute myeloid leukemia (AML) are urgently needed; treatment has not changed significantly over the…
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