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.
A work-stretched US FDA has several key approval application still to review by the end of 2023.
Curiously, however, higher dosing does not seem to be the answer to the company’s relapse problem.