RE: RE: Ray IMO.6 Apr 2019 22:54
Well big pharma have not been convinced about cancer vaccines.
More interested in TCR and CarT.
So, Scancell are having to run more trials to convince them
Hence SCIB1 combo and SCIB2 combo.
Yes, this makes immunobody more attractive (see Slide 15) for mouse results.
So, if either of these trials acheives Lindy's endpoint then big pharma will have a change of heart about cancer vaccines IMO.
Then, on top of that we have Moditope. This has already attracted a lot of attention from the scientific community.
Lindy believes that this does not require the help of a CI. It does the job on its own.
Have a look at slide 8 to give you some idea of its success in mouse experiments - 100% survival
Then 2 of the Modi1 targets are the subject of the collaboration with BionTech.
I'm not going to say that the SP isn't important, but I am saying its barmy IMO.
From slide 8
"Vimentin and enolase targets are highly expressed in triple negative breast cancer (TNBC) (90%), ovarian cancer (95%)," and sarcoma (100%) - all with high unmet medical need
A bit out of date, since sarcoma has now been replaced with head and neck cancer in the Modi1 trial.
Consider, if the Modi1 trial gives comparable results to the mouse experiments.
What then........?