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Re: None

Tuesday, 10/11/2016 3:02:38 PM

Tuesday, October 11, 2016 3:02:38 PM

Post# of 346543
My first quick opinion on yesterday's PR is kudos to the company for getting the resources to determine beta-2 GP1 as an important biomarker.

Additional questions and thoughts:

1. Why did they break out the range between 200 and 240 vs greater than 200?

2. Are they in FDA initiation for a biomarker qualification submission?

3. It would be nice to see a deep dive break out of ecog 0 vs 1 vs Bavi/doce vs doce vs alternative drug treatments/ trials patients sought during the trial vs beta 2 GP1 vs patient geographics and how all of that might have effected MOS. Was or will any of that info be prepared?
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