I think you have hammered on the correct point. These patients had not responded to any of the SOC. They had no other options. A CR and SD with mid dose is an amazing result for both these patients and shareholders.
Have a look at how some CarT have been given expedited approvals after phase 2 trials with T cell tech. Those drugs have many adeverse events (a recent on with AE rate of 79%).
For IMU have a safe drug, with these kind of results is a fantastic place to be. And to think there are still another two drugs to start trials!
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