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    Home > Medical News > Medical Research Articles > FDA approves Precigen's PRGN-3006 Research New Drug (IND) Application

    FDA approves Precigen's PRGN-3006 Research New Drug (IND) Application

    • Last Update: 2020-06-10
    • Source: Internet
    • Author: User
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    Precigen, aof intrexon's wholly ownedcompany,(http:// signed a new licensing agreement with Ziopharm in October, however, Precigen announced thatFDA(http://has approved its prGN-3006 researchnew drug(http://(IND) applicationPRGN-3006
    PRGN-3006 UltraCAR-T is an autologous chimeric antigen receptor T cell (CAR-T) therapy for the treatment of recurrent or refractory acute myeloid leukemia (AML) and high-risk bone marrow hyperplasia syndrome (MDS)PRGN-3006 UltraCAR-T is a multigene CAR-T cell therapy that uses the Sleeping Beauty Platform (SB system) to express chimeric antigen receptors, membrane binding interleukin-15 (mbIL15), and control switches for recurrent or refractory AML and higher risk MDSthis phase 1 clinical dose increase study will assess the safety and maximum tolerable dose of PRGN-3006 UltraCAR-T and will be conducted in collaboration with the Moffitt Cancer Center
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