RecruitingPHASE1, PHASE2NCT06040320
Polatuzumab Vedotin (Pola) Plus Rituximab (R) in Patients With Post-transplant Lymphoproliferative Disorder (PTLD)
Studying Post-transplant lymphoproliferative 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
- Washington University School of Medicine
- Principal Investigator
- Neha Mehta-Shah, M.D., M.DWashington University School of Medicine
- Intervention
- Polatuzumab vedotin(drug)
- Enrollment
- 12 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2032
Study locations (1)
- Washington University School of Medicine, St Louis, Missouri, United States
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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