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.
Study Type
OBSERVATIONAL
Enrollment
100
Synexus Clinical Research, US INC
Wilmington, North Carolina, United States
RECRUITINGDuration of Vimseltinib Treatment
Time frame: Baseline up to 12 months
Time to Discontinuation of Vimseltinib
Time frame: Baseline to Discontinuation (Estimated up to 12 months)
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