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The Cranbury, New Jerseybased biotech announced FDA acceptance of its Biologics License Application for RP-L201 (marnetegragene autotemcel), an investigational lentiviral vector (LV)-based gene therapy for LAD-I, a rare, genetic immune disorder that predisposes patients to frequent and often fatal infections
Teichman SL, Neale A, Lawrence B, Gagnon C, Castaigne JP, Frohman LA
F.Al TarabshehT
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