With Vertex and CRISPR some 30 patients in, Editas moves forward in sickle cell patients after FDA lifts hold
With gene therapies for sickle cell disease proving all the rage, one company is getting its FDA-imposed chains removed.
Editas Medicine announced Wednesday that the FDA lifted a partial hold on an early-stage study for its sickle cell therapy. Regulators had placed the hold on the company’s EDIT-301 program and asked it to develop a new potency assay, company spokesperson Cristi Barnett tells Endpoints News.
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