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First-in-human evaluation of CO-1686, an irreversible, highly selective tyrosine kinase inhibitor of mutations of EGFR (activating and T790M).

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Year: 2014
Type: conference-abstract
Source: Journal of Clinical Oncology
DOI: 10.1200/jco.2014.32.15_suppl.8010
Authors: Lecia V. Sequist, Jean-Charles Soria, Shirish M. Gadgeel, Heather A. Wakelee, D. Ross Camidge, Andrea Varga, Benjamin J. Solomon, Vassiliki Papadimitrakopoulou, Sarah S. Jaw-Tsai, Lisa Caunt, Paramjit Kaur, Lindsey Rolfe, Andrew R. Allen, Jonathan Wade Goldman
Institutions: Massachusetts General Hospital, Institut Gustave Roussy, Wayne State University, The Barbara Ann Karmanos Cancer Institute, Stanford Cancer Institute, Stanford University, University of Colorado Cancer Center, Peter MacCallum Cancer Centre, The University of Texas MD Anderson Cancer Center, Clovis Oncology (United States), University of California, Los Angeles
Language: English

Topic: Lung Cancer Treatments and Mutations
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W2461360472
Cites:
Cited by: 143
Related to: 10
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