Pexidartinib is a selective tyrosine kinase inhibitor that works by inhibiting the colony-stimulating factor (CSF1)/CSF1 receptor pathway. Pexidartinib was originally developed by Daiichi Sankyo, Inc. and it was approved by the FDA in August 2019 as the first systemic therapy for adult patients with symptomatic tenosynovial giant cell tumor. Tenosynovial gia...
Pexidartinib is indicated for the treatment of adult patients with symptomatic tenosynovial giant cell tumor (TGCT) associated with severe morbidity or functional limitations and not amenable to improvement with surgery.
Osaka International Cancer Institute, Osaka, Japan
Kanazawa University Hospital, Ishikawa, Japan
Nagoya University Hospital, Aichi, Japan
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Leiden University Medical Center (LUMC), Leiden, Netherlands
Washington University, Saint Louis, Missouri, United States
Peking University Cancer Hospital, Beijing, China
The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China
Beijing Ji Shui Tan Hospital, Beijing, China
Clinical Pharmacology of Miami, LLC., Miami, Florida, United States
Orlando Clinical Research Center, Orlando, Florida, United States
University of Kansas Cancer Center, Westwood, Kansas, United States
University of Arizona, Tucson, Arizona, United States
HonorHealth, Scottsdale, Arizona, United States
Memorial Sloan Kettering Cancer Center, New York, New York, United States
Worldwide Clinical Trials Early Phase Services, San Antonio, Texas, United States
Centre Léon Bérard, Lyon, France
IUCT-oncopole, Toulouse, France
Memorial Sloan Kettering Cancer Center, New York, New York, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
OSU Comprehensive Cancer Center, Columbus, Ohio, United States
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