The goal of this observational study is to better understand real-world use of vimseltinib, treatment patterns, and health-related quality of life in participants treated with vimseltinib for TGCT.
This study will collect data in an observational disease registry involving no intervention to the participants and will not influence standard medical care or impact treatment decisions for participants.
Diagnosis of TGCT according to medical records
Prescribed vimseltinib per the approved label requirements. Participants are eligible if either (A) the decision to receive vimseltinib has been made but treatment has not yet been initiated or (B) the decision to receive vimseltinib has been made and participant has received first dose of prescribed vimseltinib less than 6 months prior to study enrollment
Has provided informed consent and medical records release
Participant has received any other systemic agent for the treatment of TGCT during the 6 months prior to starting treatment with vimseltinib
Participant has received the first dose of prescribed vimseltinib in the current treatment course more than 6 months before study enrollment
Participant is active in an interventional clinical trial of vimseltinib
Participants being treated for TGCT with vimseltinib in the community setting.
Cohort
Prospective
Not listed
Duration of Vimseltinib Treatment
Time to Discontinuation of Vimseltinib
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