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Thursday, October 05, 2017 9:00:37 AM
I bring this up as it relates to cost. Hypothetically if say 5% of the patients were at higher risk of life threatening complications, HER2 with legitimate life saving efficacy but side effects could still be approved (eventually) and be incredibly lucrative, but those trials and working with FDA thru the process could take some time and be very costly.
If that is true it would be logical to sell or license to a Big Pharma who could easily take on the heavy lifting and afford the cost.
Even if safety profile is no problem at all, it still makes sense to sell or license this out due to costs involved.
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