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

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Key facts

Sponsor
University of Pennsylvania
Principal Investigator
Stephen J. Schuster, MD
Abramson Cancer Center, University of Pennsylvania
Intervention
Bexxar(drug)
Enrollment
16 target
Eligibility
18-75 years · All sexes
Timeline
20072015

Study locations (1)

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.

Open NCT00434629 on ClinicalTrials.gov

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