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Thursday, September 28, 2017 2:10:08 PM
At this point, I am simply not convinced that they are actually able to convert anti-PD-1 nonresponders into responders using the current IL-12 DNA construct and electroporation device. The 33% BORR advertised is for all checkpoint inhibitor nonresponders, not just anti-PD-1 nonresponders. That is, they aren't going for anti-CTLA-4 nonresponders in the PISCES trial. This is the biggest issue I have with the company right now. I don't feel comfortable with the existing data to give me much confidence in the PISCES trial.
With all this said, the P2A-linked data, TRACE-enabled device, and multigene constructs give me a lot of faith in the company's future. I also truly like the company's leadership. I think ONCS's intratumoral gene expression platform is the best approach to eliminating solid tumors. I think there is so much locked up value in this early stage work that it has become frustrating for me to see the company languish around a $20M valuation. I have invested literally thousands of hours researching cellular biology and combing through peer reviewed data and I gotta tell ya, as soon as ONCS figures out the right combinations of encoded proteins to drive immunity, things will change very quickly. I think anti-CTLA-4 needs to be encoded on a plasmid delivered and expressed intratumorally with P2A-linked IL-12 and a co-stimulator. That is in my unprofessional opinion, but it is an informed one.
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