Of course Lindy also has a mAb for gastric cancer - FG27. This has Avidimab added. I think she would be looking for better results than that provided by bemarituzumab. Maybe this was the mAb for which a deal was almost done before Redmile threw a pile of cash at Scancell. At the 2020 AGM, she didn't actually mention a CT for FG27, only that is was being progressed
Thanks for pointing that out. I wasn't quite sure whether the document I posted related to the vaccine that the UK government has ordered. Do we know whether the new curevac vaccine is an update on their first vaccine i.e. it is taking into account known spike protein variants? If this is the case then IMO it could be still lagging behind what Covidity may provide. It could be 1st gen+ but not really 2nd gen. Your comments would be most welcome.
Quite possibly Wild. I'm hoping for a double whammy for Immunobody this year with great data in both Covidity and SCIB1/Keytruda trials. That would certainly make the world take notice.
Where Lindy's approach may prove to be superior is that she identifies specific epitopes (i.e portions of a protein) as the best to target and then Immmunobody in combination with Avidimab activates the T Cells that match those epitopes.
Because of Immunobody's dual presentation aspect the activated T Cells have high avidity (ability to stay attached to the target) and also strong clonal expansion (the T Cells splitting to produce identical copies). It is this high avidity and strong clonal expansion that may turn out to be key to Covidity's success.
As far as I know mNRA vaccines are messages to instruct the body on how to produce a protein, so yes this applies to any protein including the N protein.
This description of a clinical trial mentions the N protein in connection with antibodies but there doesn't seem to be a mention of testing a T Cell response to the N protein.
I haven't found a link for multiple vaccinations for adults. I suppose the criterion must be that the individual vaccines do not interact with each other and the mild side effects you get from each vaccine do not combine to produce more serious cumulative side effects.
"Future Research We have identified a common process that occurs in most cancer that can be recognised by the immune system. This would allow us to design a vaccine to stimulate an immune response which would recognise and kill early cancerous cells. This may have to be boosted yearly as for seasonal flu vaccines. It could be given to people at high risk of cancer or to adults over 60 which are the most common age group for this disease."
You cannot fault Lindy on the scale of her ambition.
The PhD previously discussed for investigating administration of Covidity intradermally and/or by inhalation looks like it is aimed at vaccinating large populations of the poorer countries. If CEPI were to support Covidity they would obviously want to accelerate that research.