RecruitingPhase 3NCT06930794
A Study of Vebreltinib and Platinum-Containing Double Agents in Subjects With MET-Positive
Studying NLRP3-associated autoinflammatory disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Beijing Pearl Biotechnology Limited Liability Company
- Principal Investigator
- Yilong Wu, MDGuangdong Provincial People's Hospital
- Intervention
- Vebreltinib combined with platinum-based doublet chemotherapy.(drug)
- Enrollment
- 300 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2030
Study locations (2)
- Cancer Hospital Chinese Academy of Medical Sciences, Beijing, Beijing Municipality, China
- Guangdong Provincial People's Hospital, Guangzhou, Guangdong, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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