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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