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GSK2256098
Known as:
FAK Inhibitor GSK2256098
, Focal Adhesion Kinase Inhibitor GSK2256098
A focal adhesion kinase-1 (FAK) inhibitor with potential antiangiogenic and antineoplastic activities. FAK inhibitor GSK2256098 inhibits FAK, which…
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National Institutes of Health
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Related topics
Related topics
4 relations
Broader (2)
Aminopyridines
Hydroxamic Acids
NCIt Antineoplastic Agent Terminology
Receptor Tyrosine Kinase Inhibition
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2020
Review
2020
FAK-targeted and combination therapies for the treatment of cancer: an overview of phase I and II clinical trials
Atish Mohanty
,
Rebecca R Pharaon
,
Arin Nam
,
S. Salgia
,
Prakash Kulkarni
,
E. Massarelli
Expert Opinion on Investigational Drugs
2020
Corpus ID: 212741434
ABSTRACT Introduction: Focal adhesion kinase (FAK) is a promising target for the treatment of solid tumors because its expression…
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Highly Cited
2019
Highly Cited
2019
A phase Ib dose-finding, pharmacokinetic study of the focal adhesion kinase inhibitor GSK2256098 and trametinib in patients with advanced solid tumours
G. Mak
,
J. Soria
,
+13 authors
H. Arkenau
British Journal of Cancer
2019
Corpus ID: 116864311
Combined focal adhesion kinase (FAK) and MEK inhibition may provide greater anticancer effect than FAK monotherapy. This dose…
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Highly Cited
2019
Highly Cited
2019
WT1 associated protein promotes metastasis and chemo-resistance to gemcitabine by stabilizing Fak mRNA in pancreatic cancer.
Bing-Qi Li
,
Z. Liang
,
+5 authors
Yupei Zhao
Cancer Letters
2019
Corpus ID: 73487379
2019
2019
BI 853520, a FAK-Simile of Prior FAK Inhibitors?
Rachael Chang Lee
,
H. Gan
Targeted oncology
2019
Corpus ID: 71143814
2018
2018
A phase II trial of GSK2256098 and trametinib in patients with advanced pancreatic ductal adenocarcinoma (PDAC) (MOBILITY-002 Trial, NCT02428270).
K. Aung
,
E. Mcwhirter
,
+13 authors
P. Bedard
2018
Corpus ID: 79935239
409Background: MEK (mitogen-activated protein kinase kinase) is activated through mutated KRAS in > 90% of PDAC. Focal adhesion…
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2015
2015
A phase Ib dose-escalation study of GSK2256098 (FAKi) plus trametinib (MEKi) in patients with selected advanced solid tumors.
H. Arkenau
,
A. Gazzah
,
+15 authors
L. Yan
2015
Corpus ID: 79032740
2593 Background: The focal adhesion kinase (FAK) and MAPK pathways share common upstream activators and contribute to cell…
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2015
2015
PTEN Expression as a Predictor of Response to Focal Adhesion Kinase Inhibition in Uterine Cancer
D. Thanapprapasr
,
R. Previs
,
+10 authors
A. Sood
Molecular Cancer Therapeutics
2015
Corpus ID: 3259254
PTEN is known to be frequently mutated in uterine cancer and also dephosphorylates FAK. Here, we examined the impact of PTEN…
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2015
2015
ATNT-06EVALUATION OF THE SAFETY OF GSK2256098 AND PHARMACOKINETICS OF 11C-GSK2256098 IN PATIENTS WITH RECURRENT GLIOBLASTOMA BY POSITRON EMISSION TOMOGRAPHY (PET) IMAGING.
P. Mulholland
,
M. Williams
,
+13 authors
S. Blagden
2015
Corpus ID: 75847102
BACKGROUND: Focal adhesion kinase (FAK) is overexpressed in glioblastoma (GBM) and is associated with poor prognosis. The FAK…
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2012
2012
Phase I clinical and pharmacologic study of the focal adhesion kinase (FAK) inhibitor GSK2256098 in pts with advanced solid tumors.
J. Soria
,
Hui K. Gan
,
+16 authors
M. Millward
2012
Corpus ID: 79118964
3000 Background: FAK has an important role in cancer invasion and metastasis. FAK and phospho-FAK (pFAK) are increased in…
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Review
2011
Review
2011
Clinical importance and potential use of small molecule inhibitors of focal adhesion kinase.
A. Schultze
,
W. Fiedler
Anti-Cancer Agents in Medicinal Chemistry
2011
Corpus ID: 46056198
Since its first description Focal Adhesion Kinase (FAK), a cytoplasmatic tyrosine kinase, has been implicated in the formation…
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