If CF33 can provide the framework for other solid cancer treatment then easily $50B MC. The FDA won't even need IMU to demonstrate safety again after the approval for CF33, IMU just need to demonstrate efficacy for the other solid cancer treatment so what's an even faster path than "Fast Track".........
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- Ann: FDA Fast Track Designation Granted for VAXINIA Trial Program
Ann: FDA Fast Track Designation Granted for VAXINIA Trial Program, page-347
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