Dacomitinib, designed as (2E)-N-16-4-(piperidin-1-yl) but-2-enamide, is an oral highly selective quinazalone part of the second-generation tyrosine kinase inhibitors which are characterized by the irreversible binding at the ATP domain of the epidermal growth factor receptor family kinase domains.
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Dacomitinib is indicated as the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletion or exon 21 L858R substitution mutations as verified by an FDA-approved test.
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Erasmus Medical Center Cancer Institute, Rotterdam, Netherlands
The Netherlands Cancer Institute, Amsterdam, Netherlands
University Medical Center Utrecht, Utrecht, Netherlands
Dana Farber Cancer Institute, Boston, Massachusetts, United States
Medical University of South Carolina/ University Hospital, Charleston, South Carolina, United States
MUSC Health East Cooper, Mount Pleasant, South Carolina, United States
UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, United States
Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute, Los Angeles, California, United States
Investigational Drug Service, Hillman Cancer Center, Pittsburgh, Pennsylvania, United States
Princess Margaret Cancer Centre, Toronto, Ontario, Canada
Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy
Pfizer Investigational Site, South Miami, Florida, United States
City of Hope, Duarte, California, United States
St. Jude Heritage Healthcare, Fullerton, California, United States
UC San Diego Medical Center - La Jolla, La Jolla, California, United States
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