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Real-World Patient Experience of Vimseltinib for the Treatment of Tenosynovial Giant Cell Tumor

Status: Recruiting
Location: See location...
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
United States
North Carolina
Synexus Clinical Research, US INC
RECRUITING
Wilmington
Contact Information
Primary
Clinical Team
clinicaltrials@deciphera.com
888-724-3274
Time Frame
Start Date: 2025-09-03
Estimated Completion Date: 2027-09
Participants
Target number of participants: 100
Related Therapeutic Areas
Sponsors
Leads: Deciphera Pharmaceuticals, LLC

This content was sourced from clinicaltrials.gov

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