They aren't questioning "negative" announcement of clinical trial result which IMU has never released, on the contrary they said the end of Ph2 clinical result for HER-Vaxx were excellent. There's still a market for HER-Vaxx as Chemotherapy will be the last option for cancer patient so why would patient want to use a drug which minimise the affect of using Chemo where in some instance it's actually the radiation which cause the death and not the cancer???
What they are questioning is the path for HER-Vaxx and PD1-Vaxx which are both at the most advanced development stage of all of IMU's IP. I think right now management is focusing on these 3 IP as they have FDA IND so BP will more than likely purchase the company once they are at similar development stage.
Why IMU is a multi multi bagger, page-24732
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