CRISPR Ther­a­peu­tics gets a snap­shot of off-the-shelf CAR-T suc­cess in B-cell ma­lig­nan­cies — marred by the death of a pa­tient

Just days af­ter sci­en­tif­ic founder Em­manuelle Char­p­en­tier shared the No­bel prize for her work on CRISPR/Cas9, CRISPR Ther­a­peu­tics $CR­SP is show­ing off a snap­shot of suc­cess in their ear­ly-stage study for an off-the-shelf CAR-T ap­proach to CD19+ B cell ma­lig­nan­cies — a snap­shot marred by the death of a pa­tient who had been giv­en a high dose of the treat­ment.

Us­ing their gene edit­ing tech, re­searchers for CRISPR en­gi­neered cells from healthy donors in­to an at­tack ve­hi­cle aimed at can­cer, some­thing that has been achieved with great suc­cess us­ing pa­tients’ own cells — the au­tol­o­gous ap­proach. But au­tol­o­gous CAR-T is ham­pered by the more com­plex vein-to-vein re­quire­ment that de­lays treat­ment, and now CRISPR Ther­a­peu­tics along with oth­er play­ers like Al­lo­gene are de­ter­mined to re­place the pi­o­neers with CAR-T 2.0.

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