Brigatinib, originally named AP26113, is a reversible dual inhibitor of anaplastic lymphoma kinase (ALK) and epidermal growth factor receptor (EGFR). It presents selectivity against the mutant forms of EGFR compared to the wild-type. It also exhibits selectivity against 9 different Crizotinib-resistant mutants of the EML4-ALK fusion gene, which is a pivotal ...
The anaplastic lymphoma kinase positive, metastatic non-small cell lung cancer (ALK+ NSCLC), represents only 3-5% of the NSCLC cancer cases, but the ALK mutation, overexpression and presence in several oncogenic fusion proteins in solid and hematologic tumors have pointed out the importance as well as its potential as a cancer therapy target. The ALK-related...
City of Hope, Duarte, California, United States
University of Colorado Hospital, Aurora, Colorado, United States
Mayo Clinic, Rochester, Minnesota, United States
I.R.S.T. Srl Irccs, Meldola, Italy
Ospedale Classificato Sacro Cuore - Don Calabria, Negrar, Italy
I.R.C.C.S. Istituto Oncologico Veneto, Padova, Italy
UCLA Medical Center, Los Angeles, California, United States
University of Miami, Miami, Florida, United States
New York University Langone Medical Center, New York, New York, United States
Universitätsmedizin Essen, Essen, Germany
Evangelisches Krankenhaus Hamm, Hamm, Germany
Lungenklinik Hemer, Hemer, Germany
Northwestern University, Chicago, Illinois, United States
Penn State Cancer Institute, Hershey, Pennsylvania, United States
Rush University Medical Center, Chicago, Illinois, United States
Hospital Regional Universitario de Málaga, Málaga, Andalucia, Spain
Hospital Clínico de Salamanca, Salamanca, Spain
Hospital General de Valencia, Valencia, Spain
National Cancer Center, Goyang-si, Gyeonggi-do, Korea, Republic of
University of California, San Francisco, San Francisco, California, United States
Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States
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