@JB1975
In the USA :
”Patent applications generally are published about 18 months after they are initially filed.”
https://www.mintz.com/insights-center/viewpoints/2231/2023-12-06-basics-how-inventors-own-work-affects-patent
As you still are unaware of this fact, i thought i would provide you with a basic teach in from some IP specialist patent lawyers. Link above
Not long to go before i can show you the relevant patent
Let me know if you want me to find another five quoted examples before you accept the point ?
Aww shucks, let’s try another link , because i know how sceptical you are .
https://www.nutter.com/ip-law-bulletin/nutter-patent-basics-part-1-what-happens
@nippy
I believe the need for this assay is risk management of upstream CQA’s which may have identified potency shortfalls in the harvesting of cells from the Osiris facilty in the USA, had it been available for use at the time? It may represent also an extremely useful quality control process going forward to monitor factors which influence downstream potency, which will be the envy of the industry if authorised…..another massive IP barrier to entry…but no doubt available for licence at the right price. I suggest JB1975 looks at the MAGIC algorithm for acute GVHD which risk stratifies patients , to see an example of how a panel of data can be forged into a matrix assay shown in terms of straightforward numerical values, below and above the AUC.
Enough said , I have several companies on my radar right now, so forgive me if I can’t reply to all the other posters…i just don't have the time ! OP
Please do not rely on the facts or opinions expressed in this post when making an investment decision . I am not a medical or legal professional so do your own due diligence .
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