I think that with a compromised immune system CF33 is as effective as most Oncolytic viruses maybe there an are some substantially better and some substantially worse. If it were just an Oncarlytic treatment then I would be out, but my understanding is that it has been engineered to excise an immune response and that is the point of difference between CF33 and other Oncarlytic treatments.
If I am mistaken please let me know but if that is the case then a functioning immune system would be helpful to response rates. what stage of chemotherapy were the mice at when their tumours were obliterated?
If CF33 truly was a failure what would we be expecting from Management?
I would expect to see different behaviour to what I am seeing, again happy to be proven wrong here.![]()
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