As to the FDA, I believe if they show this two month separation or better at trial's end, the drug will be approved based on the SPA. The better the drug functions, obviously, the better the profit margin will be... premium pricing for more survival, less pricing for less survival. If we get several complete responders/partial responders as contrasted to Avastin.... say 28 percent response rate versus 10 percent response rate for Avastin only as the phase II showed, this will be a meaningful secondary endpoint.
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