CompletedPhase 1NCT00434629
Safety and Efficacy of Bexxar Therapy in the Treatment of Relapsed/Residual B-Cell Lymphoma After Autologous Transplant
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
- University of Pennsylvania
- Principal Investigator
- Stephen J. Schuster, MDAbramson Cancer Center, University of Pennsylvania
- Intervention
- Bexxar(drug)
- Enrollment
- 16 target
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2007 – 2015
Study locations (1)
- Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania, United States
Collaborators
GlaxoSmithKline
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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