The patent tells us who will respond. How long do you think it will take trial data to convince a DSMB that it works if every patient entered responds to treatment by 8 weeks and tumors collapse to become operable or disappear within a month or 2 later? It’s always what they don’t say or talk about anymore. Best wishes.
''We are currently conducting a 60-patient Phase I/II trial of DCVax-Direct for all types of inoperable solid tumors. The trial is under way at MD Anderson in Houston, TX and MD Anderson in Orlando, FL, with additional sites in varying stages of preparation. The Phase I stage of the trial involves dose escalation, testing 3 different dose levels of DCVax-Direct, and confirmation of the optimal dose. The Phase II stage of the trial will focus on efficacy. The primary measure of efficacy will be regression (i.e., shrinkage or elimination) of the patient’s existing inoperable tumors. Such regression is a rapid endpoint: if it is going to occur, is anticipated to occur within a couple months of treatment.'' https://nwbio.com/dcvax-direct/
You're right on BIO. Direct is the "800lb Gorilla in the Room". Amazing how LP has kept it under the radar. Any accurate publicity will overwhelm DC Vax L.