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GDC-0973
Known as:
MEK Inhibitor GDC-0973
, XL518
National Institutes of Health
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Related topics
Related topics
3 relations
Broader (2)
Azetidines
Piperidines
Narrower (1)
Cobimetinib
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
BCL-2 Inhibitor Venetoclax (ABT-199) and MEK Inhibitor GDC-0973 Synergise to Target AML Progenitors and Overcome Drug Resistance with the Use of PET Scanning in a Mouse Model of HR-MDS to Monitor…
R. Padua
,
L. Sarda-Mantel
,
+16 authors
C. Chomienne
Blood
2018
Corpus ID: 208420233
Introduction: Targeted drugs are needed for HR-MDS/AML, particularly in elderly patients and Venetoclax, approved for some CLL…
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2014
2014
Abstract CT328: Clinical results of a phase Ib dose-escalation study of the Mek inhibitor cobimetinib (GDC-0973) and the Akt inhibitor ipatasertib (GDC-0068) in patients (pts) with solid tumors
J. Bendell
,
P. LoRusso
,
+7 authors
G. Shapiro
2014
Corpus ID: 72751236
Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA Introduction: Co-activation of Mek and Akt signaling…
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2012
2012
Abstract 911: Vemurafenib FDG-PET preclinical imaging outcomes across BRAF V600E mutant and resistant tumors
A. Baudy
,
Taner Dogan
,
+4 authors
Simon-Peter Williams
2012
Corpus ID: 72240358
The BRAF inhibitor vemurafenib (marketed as zelboraf) has recently been FDA approved for the treatment of metastatic melanoma in…
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2012
2012
Abstract P6-04-11: Combination of PI3K-AKT-mTOR and MEK-ERK pathway inhibitors overcome acquired resistance to letrozole in ER+ breast cancer models
P. De
,
Y. Sun
,
L. Friedman
,
S. Chen
,
N. Dey
,
B. Leyland-Jones
2012
Corpus ID: 72194688
Background: Approximately 60–70% of breast cancers (BC) express estrogen receptor (ERα) and/or progesterone receptor (PR), the…
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2011
2011
Abstract LB-89: Clinical combination of the MEK inhibitor GDC-0973 and the PI3K inhibitor GDC-0941: A first-in-human phase Ib study in patients with advanced solid tumors
J. Bendell
,
P. LoRusso
,
+9 authors
G. Shapiro
2011
Corpus ID: 72076217
Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL Introduction : The RAS/RAF/MEK/ERK and PI3K/PTEN/AKT…
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2011
2011
Abstract 1304: Clinical pharmacokinetics of GDC-0973, an oral MEK inhibitor, in cancer patients: data from a Phase 1 study
L. Musib
,
S. Eppler
,
+13 authors
J. Ware
2011
Corpus ID: 58732080
Background: GDC 0973 is a potent, selective, orally administered MEK1/2 inhibitor. It has shown antitumor activity in preclinical…
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2011
2011
Abstract 1280: Preclinical and Clinical Evidence for MEK Pathway Inhibition by GDC-0973 using FDG-PET
Simon-Peter Williams
,
J. Fredrickson
,
+9 authors
A. Crespigny
2011
Corpus ID: 71496580
Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL Inhibitors of the mitogen-activated protein kinase…
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2010
2010
132 Intermittent dosing of the MEK inhibitor, GDC-0973, and the PI3K inhibitor, GDC-0941, results in prolonged accumulation of Bim and causes strong tumor growth inhibition in vivo
M. Belvin
,
L. Berry
,
+7 authors
K. Rice
2010
Corpus ID: 71998098
2008
2008
A phase 1 dose-escalation study of XL518, a potent MEK inhibitor administered orally daily to subjects with solid tumors
L. Rosen
,
P. Galatin
,
+5 authors
B. Sikic
2008
Corpus ID: 74731985
14585 Background: XL518 is a potent, selective, orally bioavailable inhibitor of MEK1, a component of the RAS/RAF/MEK/ERK pathway…
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2007
2007
XL518, a potent selective orally bioavailable MEK1 inhibitor, downregulates the RAS/RAF/MEK/ERK pathway in vivo, resulting in tumor growth inhibition and regression in pre-clinical models
S. Johnston
2007
Corpus ID: 85681118
C209 Activation of the Ras/Raf/MEK/Erk pathway is a frequent occurrence in human tumors and often results from mutational…
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