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bfiest

01/14/18 11:34 PM

#322616 RE: corporalagarn #322615

It’s evident the market has no idea what the IP is worth at this point. The market is certainly questioning whether the IP is worth anything at this point. That’s what the market is saying and without evidence to the contrary the market will continue to say this — resulting in a depressed stock price. But this story is just starting to unfold. It is just now becoming hopefully a “true” and dynamic situation and can change on a dime. We will all know soon enough what the market determines the value to be. All the predictions in the world cannot change that. So we wait and hope. I only want a fair process to be utilized. To me that is all we can ask. I for one am more optimistic than I have been in a very long time. Optimistic that we will get fair play for once. Let the process unfold. Predictions of any kind are simply an amusing way to pass the time. None of us really have any idea. Now do we? And yes we are representative of the market albeit a small sub section. The market will speak soon enough. That is the only certainty. It’s certainly premature to believe it has already spoken. AIMO
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jakedogman1

01/14/18 11:50 PM

#322617 RE: corporalagarn #322615

The question will come down to how much BP wants to find out whether the sunrise data set is real and if so, what is the value of treating "cold tumors".... does it increase the "footprint" of that subgroup enough to be commercially viable...

keep in mind the entire sunrise ICI subgroup was heavily weighted to less than 1% pdl 63% vs say 34% in the merck keynote 10 study... mgmt had a specific question related to "cold tumors"

And how much is it worth to answer the car-t question? And exosomes...

At the end of the day it will be whether BP can identify a population where bavi by using biomarkers ...

Keep in mind about $500 mil (or more) has been spent to date...

And 5,000 patients at $100k per treatment is $500 mil a year

and billions are at stake for BP...

So $500 mil is not a reach at all and could be much higher and it could be $5 mil.....

The issue has been terrible mgmt of the IP and taking a risk of going alone and no coverage or institutional interest or desire by prev mgmt in order to keep the gravy train... so there could be a real disconnect to value and SP... BP has beat the bastards into submission... so we will soon see what the IP is worth and we are fortunate that BP in general has the motivation to improve ICI outcomes and cash ...

https://investorshub.advfn.com/boards/read_msg.aspx?message_id=135586168


https://www.keytruda.com/static/pdf/keytruda-pd-l1-expression-testing-guide.pdf

RESULTS: 93 of 597 randomized patients (16%) received ICI as next line of therapy after SUNRISE assigned treatment. Baseline characteristics were balanced between the treatment groups and consistent with the ITT population. From randomization, mOS was not reached (95% CI, 15.2-NA) in D+B (N=46) and 12.6mos. (95% CI, 10.4-17.8) in D+P (N=47) (HR, 0.46; P=0.006). From start of ICI, mOS was not reached (95% CI, 10.2-NA) in D+B and 6.2mos. (95% CI, 3.9-8.7) in D+P (HR, 0.42; P=0.002). The mPFS was 6.0mos. (95% CI, 3.5-6.5) in D+B and 4.4mos. (95% CI, 2.6-6.3) in D+P (HR, 1.00; P=0.991). ORR was 20% vs. 13% (Odds ratio 0.6; P=0.41) for D+B and D+P, respectively. The safety profile was similar between groups and no immune related (IR) toxicities (colitis, pneumonitis, hypothyroidism) were reported.
CONCLUSIONS: Within the limits of a subgroup analysis, a significant improvement in OS was observed for patients previously treated with D+B. Furthermore, bavituximab has not been associated with IR toxicities and might serve as a useful drug in combination with ICI for the treatment of immune cold tumors.