Rich Horgan (L) with his late brother, Terry (Cure Rare Disease via YouTube)

N-of-1 CRISPR tri­al ends with a death as non­prof­it digs in­to what hap­pened

Al­most two months af­ter the non­prof­it Cure Rare Dis­ease re­ceived FDA clear­ance to ad­min­is­ter its first-in-hu­man CRISPR ther­a­peu­tic for Duchenne mus­cu­lar dy­s­tro­phy, the non­prof­it an­nounced that the one pa­tient in the tri­al, Ter­ry Hor­gan, the broth­er of the non­prof­it’s founder and CEO, Rich Hor­gan, passed away.

Re­searchers are still try­ing to fig­ure out what ex­act­ly hap­pened with the sin­gle shot CRISPR ther­a­py, the non­prof­it said in a state­ment, and that process may take up to four months.

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