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...
Fondazione Policlinico Gemelli IRCCS, Rome, Italy
MD Anderson Cancer Center, Houston, Texas, United States
Celerion, Inc., Tempe, Arizona, United States
Pfizer Norway, Oslo, Norway
Department of Oncology, Shanghai pulmonary hospital, Shanghai, Shanghai, China
CHU Angers, Angers, France
Caen - CHU, Caen, France
Hôpital de Marseille, Marseille, France
Yonsei University Health System, Severance Hospital, Seoul, Korea, Republic of
Takeda Selected Site, Tokyo, Japan
Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands
Institut Gustave Roussy, Paris, France
Pfizer Innovations AB, Sollentuna, Sweden
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