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LGX818
Known as:
Raf Kinase Inhibitor LGX818
An orally available Raf kinase inhibitor with potential antineoplastic activity. LGX818 specifically inhibits Raf kinase, a serine/threonine enzyme…
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National Institutes of Health
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Related topics
Related topics
2 relations
NCIt Antineoplastic Agent Terminology
Broader (1)
encorafenib
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Abstract CT136: Final biomarker analysis of the phase I study of the selective BRAF V600 inhibitor encorafenib (LGX818) combined with cetuximab with or without the α-specific PI3K inhibitor alpelisib…
J. Schellens
,
R. V. Geel
,
+17 authors
J. Tabernero
2015
Corpus ID: 56559135
Background: Although BRAF V600-mutated (BRAFm) colorectal carcinoma (CRC) does not generally respond to BRAF inhibitors, results…
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2015
2015
Successful implementation of a novel trial model: The Signature program.
J. Peguero
,
J. Knost
,
+16 authors
S. Piha-Paul
2015
Corpus ID: 78972479
106 Background: Here we describe 8 ongoing single agent clinical protocols under Novartis’ “Signature” program involving…
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2015
2015
Drug combo beneficial in colorectal cancer.
Cancer Discovery
2015
Corpus ID: 11207962
The BRAF V600E mutation, well documented in melanoma, is also present in approximately 8% of patients with colorectal cancer…
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2015
2015
Abstract 2140: Dual Wnt and EGFR-MAPK dependency ofBRAFV600E-mutant colorectal cancer
Youzhen Wang
,
Michael R. Palmer
,
+12 authors
M. Mclaughlin
2015
Corpus ID: 78540828
Aberrant Wnt pathway activation due to inactivating mutations in the gene encoding RNF43 (an E3 ubiquitin ligase that promotes…
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2014
2014
Abstract 5466: The Mdm2 inhibitor, NVP-CGM097, in combination with the BRAF inhibitor NVP-LGX818 elicits synergistic antitumor effects in melanoma
H. Wang
,
Matthew Zubrowski
,
+9 authors
Ensar Halilovic
2014
Corpus ID: 70914841
Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA RAF kinase inhibitors have shown substantial therapeutic…
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2014
2014
11LBA Phase I study of the selective BRAFV600 inhibitor encorafenib (LGX818) combined with cetuximab and with or without the α-specific PI3K inhibitor alpelisib (BYL719) in patients with advanced…
J. Tabernero
,
R. V. Geel
,
+17 authors
J. Schellens
2014
Corpus ID: 72996242
2014
2014
Highlights of melanoma research presented at the 49th annual meeting of the American Society of Clinical Oncology in Chicago, 2013
C. Krepler
,
D. Herlyn
Pigment Cell & Melanoma Research
2014
Corpus ID: 165448
No: 9010). This antibody exhibited much lower toxicity in patients with melanoma (n = 45) than the anti-PD1 and anti-CTLA-4…
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2014
2014
Effect of the BRAF inhibitor LGX818 on endoplasmic reticulum stress and sensitivity of NRAS-mutant melanoma cells to the MEK inhibitor binimetinib.
F. Meier
,
C. Garbe
,
+5 authors
H. Niessner
2014
Corpus ID: 59257106
9062 Background: The BRAF inhibitors vemurafenib and dabrafenib have demonstrated antitumor activity in patients with metastatic…
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2014
2014
The development of the BRAF inhibitor encorafenib (LGX818) and mitogen-activated protein kinase kinase inhibitor binimetinib (MEK162) in patients with metastatic melanoma
R. Dummer
,
K. Flaherty
,
+4 authors
D. Schadendorf
2014
Corpus ID: 218748681
2012
2012
Abstract 5592: Modeling the evolution of resistance to RAF inhibitors in clinically relevant melanoma models
M. Thakur
,
Fernando Salangsang
,
N. Pryer
,
D. Stuart
,
M. McMahon
2012
Corpus ID: 58390496
Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL Small molecule RAF inhibitors such as Vemurafenib…
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