Comment by
ScienceFirst on Apr 19, 2022 6:20pm
450-days of 20-25 patients is what the FDA probably requires, so it can better assess both CR% and DR%. That's probably why TLT puts the BDt designation around Dec. 2022 and then commercial revenues Jan. 2023 whether from a jv upfront or via the Accelerated Approval program that allows you to get revenues from the drug while being in a clinical study.