MOVE: Tenosynovial Giant Cell Tumor (TGCT) Real-World Participant Experience With Vimseltinib
Condition(s) studied
Study summary
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.
Eligibility
Primary outcome measure(s)
- Duration of Vimseltinib Treatment — Baseline up to 12 months
- Time to Discontinuation of Vimseltinib — Baseline to Discontinuation (Estimated up to 12 months)
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Synexus Clinical Research, US INC | Wilmington | North Carolina | Recruiting |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07075471 on ClinicalTrials.gov ↗ ← All trials in the USA