While I appreciate your response, you're effectively saying that you're comfortable with how IMU is progressing PD1-VAXX because of what a now ex-employee has told you...
The data you're referring would appear to be the preclinical model work on PD1-VAXX produced by Ohio State Uni.
https://static1.squarespace.com/static/5b63d41b3e2d09b1f56bf483/t/62156d4f47397c1133df7c25/1645571463514/IMU+Science+Series+PD1-Vaxx+Feb2021.pdf
https://cancer.osu.edu/news/therapeutic-pd1-cancer-vaccine-shown-to-be-safe-and-effective-in-preclinical-studies
Let's hope this translates well to humans.
And just to re-state my position on PD1-VAXX again - I think the 25% CR rate in cohort 1 (i.e. 1/10 the dose of the final cohort 3 which achieved 0 CRs) of the Imprinter trial was very interesting and I think IMU may have dropped the ball on this one (this was produced as a result of a single agent PD1-VAXX regime). This is why I'd like to understand the dose regime for NeoPOLEM.
However, this doesn't address the elephant in the room:
P.S. Still no idea how much this will cost IMU with maybe $20m cash on hand...
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