Crispr abandons first-generation Car-T projects
The company hopes that new edits could solve the relapse problem with allogeneic Car-Ts.
The company hopes that new edits could solve the relapse problem with allogeneic Car-Ts.
The once-hyped group’s most advanced hope is an allogeneic CD19 Car-T, where competition is fierce.
Curiously, however, higher dosing does not seem to be the answer to the company’s relapse problem.