sherlock: Thanks for another great post. We're going to

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Jake2212 sherlock57 #162746
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sherlock: Thanks for another great post. We're going to have to start calling you ohm jr. I know that you are trying hard to dumb down your explanations of the biological markers/info by which you reach Leronlimab focused conclusions but, unfortunately, for someone like me, you will have to get dumber.

Are you saying that your research compels you to expect "great ORR and OS data in the mCRC trial" when the ICIs are given because CYDY, with Creatv's assistance, is using a more predictively reliable biomarker test (focused on CCL3/4 levels) to determine which patients will eventually respond beneficially to an ICI? Likewise, are you expecting that LL's CRC ORR and OV data as computed before ICIs are given will be appreciably better than the ORR and OS data from the 2021 LL TNBC and CRC trials? If so, why? Better pre screening?

I assume you are not saying that CYDY has somehow improved the efficacy of LL since 2021, but I am flummoxed by your wording"that CYDY added CCL2 to the protocol as a defensive screen." "Added" how? And "protocol" for what? 

Any help you can supply to my poor old brain would be appreciated. Although obviously not tracking everything, I was able to discern that the developments you discuss have significantly increased your already steadfast confidence that Leronlimab will in fact be the game changer that we and cancer patients are counting on. And that is most definitely something to appreciate.

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