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.
But the FDA’s investigation looks like worse news for autoimmune disease than oncology.
Novartis and Gracell place further bets on shortened production times, with Bristol waiting in the wings.
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.