Catalyst

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FDA Clearance to Initiate Two Phase 3 Clinical Studies to Evaluate Tabelecleucel in Patients with Rituximab-Refractory Epstein-Barr Virus Associated Post-Transplant Lymphoproliferative Disorder (EBV+PTLD)

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Catalyst Date
Occurred on:
Dec 29, 2017
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Related Keywords Tabelecleuce, Rituximab, Lymphoproliferative Disorder